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Science Feature Articles</p>

Bring On the Rain

English

 

A fast-paced rain dance inside clouds brings on rainfall, shows a new Weizmann study. The findings, published in Nature, may provide an effective tool for rain prediction.
 
The Weizmann team has revealed that turbulent whirlpools within clouds spin heavy droplets outward, much like a sling whirled around to discharge a stone by centrifugal force, a phenomenon the scientists call the “sling effect.”
Rain dance . illustration
 
Droplets hurled by a turbulent whirlpool are more likely to collide with one another than are droplets floating peacefully about. Colliding droplets form heavy, rain-producing drops. The team – Prof. Gregory Falkovich of the Physics of Complex Systems Department, graduate student Alexander Fouxon and visiting scientist Dr. Michael Stepanov – has developed a formula that makes it possible to calculate the speed with which tiny droplets in clouds cluster into the rain-producing drops. By predicting the collision rate of droplets in a turbulent cloud, the formula makes it possible to forecast when the cloud will produce rain.
 
Emergence of raindrops from the cloud occurs in two stages. First, tiny moisture droplets condense and gradually grow until they reach a diameter of about 20 micrometers (20 thousandths of a millimeter). At this size, the droplets begin crashing into one another and gathering into larger drops about a millimeter across.
 
The collisions are caused mainly by turbulent airflow, creating whirlpools and eddies inside the cloud. Since turbulent flows of different magnitudes exist in all clouds, the Weizmann Institute formula, which includes such variables as temperature, humidity and wind speed, may prove useful for improving the precision of numerous meteorological forecasts.
 
Prof. Gregory Falkovich’s research is supported by the Gabriel Alhadeff Research Fund and the Edward D. and Anna Mitchell Family Foundation.

 

 
Space & Physics
English

Lord of the Ring

English
 
Prof. Avi Minsky. The trick of survival
 
Solving a longstanding mystery, Weizmann Institute scientists have found what makes a certain bacterium the most radiation-resistant organism in the world. The microbe’s DNA is packed tightly in a unique ring-like structure, which keeps pieces of DNA broken by radiation in close enough proximity for repair to occur.
 
The red-colored bacterium Deinococcus radiodurans can withstand 1.5 million rads – 3,000 times more than humans. Its healthy appetite has made it a reliable worker at waste sites, where it eats up nuclear waste, transforming it into safer derivatives. The ability to withstand other extreme stresses, such as dehydration and low temperatures, makes the microbe one of the few life forms found on the North Pole. It’s not surprising, then, that it has been the source of much curiosity worldwide, with Russian scientists proposing that it originated on Mars, where radiation levels are higher.
 
DNA is the first part of a cell to be damaged by radiation. The most lethal damage is the breakage of both DNA strands. While most cells, including human cells, can mend only a few such breaks in their DNA, D. radiodurans can fix more than 200. This outstanding performance caused scientists to believe that the microbe must possess uniquely effective DNA repair enzymes; yet a series of experiments found that the microbe’s repair enzymes were very similar to those in ordinary bacteria.
 
Using an assortment of optical and electron microscopy methods, Prof. Avi Minsky of the Institute’s Organic Chemistry Department has now shown that the microbe’s resilience lies in the unique ring-like structure containing its DNA, which, following radiation damage, holds severed pieces of DNA closely together, allowing for repair. This is in contrast to most other organisms, where radiation breaks the DNA into fragments that float off into the cell’s liquids and are lost. 
 
“Exciting as these findings may be, I don’t expect them to boost the protection of humans from radiation. Our DNA is structured in a fundamentally different manner,” says Minsky. “The results may, however, lead to a better understanding of DNA protection in sperm cells, where a ring-like DNA structure has also been observed.”
 

More survival tricks

 

Minsky’s team also found that the microbe undergoes two phases of DNA repair. During the first phase the DNA repairs itself within the ring as described. It then performs an even more unusual stunt.
 
The bacterium is composed of four compartments, each containing one complete copy of DNA. Minsky’s group found two small passages between the compartments. After roughly 90 minutes of repair within the ring, the DNA unfolds and migrates to an adjacent compartment – where it mingles with the copy of DNA residing there. At this point, “regular” DNA repair enzymes, common in humans and bacteria alike, kick in. To complete the mending process, the enzymes compare the two copies of DNA, using each as a template to repair the other. 
 

…and a backup system

 

Their finding of a tightly packed ring made the team wonder how the bacterium manages its everyday tasks – including protein production, for which its DNA must first unfold. How, they asked, can the microbe do this if its DNA can barely budge? This question led to the uncovering of yet another of the microbe’s survival strategies: Of the four copies of DNA, there are always two (or sometimes three) tightly packed in a ring while the other copies are free to move about. Thus at any given moment, there are copies of DNA that drive protein production and others that are inactive but continuously protected.
 

Deinococcus radiodurans. rings give protection

D. radiodurans was discovered decades ago in canned food sterilized by using radiation – setting off questions as to how it could have survived. Though these questions have now been answered, the tide of speculation as to how these defense mechanisms evolved – and where – is likely to continue.
 
Minsky, along with other scientists, believes that the bacterium’s answer to acute stresses evolved on Earth in response to a harsh environment. The very same mechanism enabling it to fight dehydration and thus survive in some of the planet’s most inhospitable deserts also protects it from the destructive effects of radiation.
 
Prof. Abraham Minsky is the incumbent of the Professor T. Reichstein Professorial Chair. His research is supported by the Helen and Milton A. Kimmelman Center for Biomolecular Structure and Assembly; TEVA Pharmaceutical Industries Ltd.; and the Verband der Chemischen Industrie.
 
Deinococcus radiodurans
Chemistry
English

The Science of Simplicity

English

Dr. Rami Marelly and Prof. David Harel. Play engine has serious uses

Ever feel you have too much on  your mind and just can't sort it our?  Imagine, then, that you were told to build a computer system that could simulate a football game and predict its development. You’d have to work on each one of the game’s many elements separately. Specifically, you’d have to take into account the physical and behavioral characteristics of each of the players and of the referees, carefully laying out the way they react to each possible set of circumstances. You’d also have to consider the features of the ball and the field, the condition of the grass, the weather and so on. Then there are the rules of the game, as well as the possibility of human error in referee decisions.

 

The numerous elements involved make building such a computerized system through regular programming virtually impossible. This is true for many other kinds of systems as well – such as aerospace systems, complex communication networks, embryonic development and even work management in the office. All include many events that trigger multiple and diverse reactions, which is why they are called “reactive systems.”

 

In the past, Prof. David Harel, Dean of the Faculty of Mathematics and Computer Science at the Weizmann Institute, created a visual programming language called Statecharts, aimed at programming reactive systems. Now, together with Dr. Rami Marelly (who worked with Harel as a graduate student), he proposes a different method that may significantly advance this field.

 

Instead of describing every component of the game separately, in what is called “intra-object” style, Harel and Marelly propose to describe the game as a collection of scenarios depicting the possible interactions between the components (what they term “inter-object” style). The approach is similar to that of a radio or TV commentator, who rather than describing characteristics of the players and the ball, describes the dynamics among them.

 

The collection of scenarios includes desirable scenarios (for example, a series of passes leading to a goal), necessary scenarios (a ball kicked upward must eventually come down), forbidden scenarios (the presence of more than 22 players on the field), and the various possible ways in which the game can progress.

 

An important aspect of the method is that it’s easy to use. A person trying to input the possible scenarios does not need a background in programming. “There is no need to write a single line of code,” says Harel. Instead of writing a cryptic input command, the programmer “plays in” the scenarios in a natural, relatively simple way. If the programmer wants to play in the “behavior” of a telephone, for example, an image of a phone appears on-screen. The programmer – which could be anyone – would “teach” the computer how he or she wants the phone to work, feeding in the desirable, necessary and forbidden scenarios. The computer, in turn, would “understand” how the different scenarios are related, and their combination would constitute the system’s full behavioral repertoire.

 

This approach is supported by a tool built by the scientists for this purpose, called the Play-Engine. It can analyze the collection of behaviors as one unit and decide, using combinations of scenarios, how to respond to changing circumstances – even those that were not directly fed into the system.

 

The new method has produced very encouraging results and is already being used to construct computer models of complex biological processes, such as the differentiation of a group of embryonic cells in the C. elegans roundworm. Although the method was only recently published in the scientific literature, numerous scientists have already found it efficient and convenient for programming reactive systems. The Play-Engine promises to produce a significant change in the programming of large systems. It may also allow people with no background in computers to easily design new programs on their PCs, specify the dynamics of their Web pages or reprogram their home appliances.

 

Harel and Marelly have authored a book called Come, Let’s Play that describes their work in detail. It will be published in May with the Play-Engine software attached so that readers can “play” on their own.

 

Out With Dead Ends

 

In a follow-up project to Harel and Marelly's work, a tool called "smart play -out”was developed by graduate student Hillel Kugler, working under the guidance of Harel and Prof. Amir Pnueli of the Computer Science and Applied Mathematics Department. Its aim is to prevent the Play-Engine from running into a dead end or other undesirable situations and to minimize surprises in the behavior of the system.

 

Prof. David Harel is the incumbent of the William Sussman Professorial Chair. His research is supported by the Arthur and Rochelle Belfer Institute of Mathematics and Computer Science; the Gulton Foundation; and the Ida Kohen Center for Mathematics Research.

 

Left to right: Dr. Rami Marelly and Prof. David Harel. Making computers play
Math & Computer Science
English

Networking Naturally

English

Dr. Uri Alon and students. basic principles from netwok motifs

 

 

Khad Gadya, the 16th-century song concluding the Passover Seder, describes a succession of allegorical events leading from the purchase of a young goat to the striking down of the Angel of Death:
 
  Father bought a young
   goat for two zuzim;
   a cat came and ate the goat;
   a dog then bit the cat;
   the dog was beaten by a stick;
   the stick was burned by fire;
   water quenched the fire;
   an ox drank the water;
   a shohet [ritual slaughterer]                              
   slaughtered the ox;
   the shohet was killed by the Angel of Death,
   who in punishment was destroyed by God.
 
Cause-and-effect chains, spanning all aspects of life, have often baffled the human mind, which is naturally inclined to find the “order” behind things. The task becomes more mind-racking as the number of factors increases. The verse above mentions a dozen factors. Now, take our DNA. How do 30,000 genes in our DNA work together to form a large part of who we are? How does one neuron operate in the context of the whole nervous system?
 
Decades of pinpointed biological research have yielded profuse bits of information. Increasingly, scientists are feeling the need to meld the many fragments together to understand how we work as a whole. In an article published in Nature Genetics, Dr. Uri Alon, a physicist at the Weizmann Institute’s Molecular Cell Biology Department, proposed a mathematical technique to seek out the basic principles of biological systems. Using this technique, he has uncovered several motifs underlying genetic, neural and food networks.   
 
Alon surmised that patterns serving an important function in nature might recur more often than statistically forecasted. This guiding principle, he thought, might help one find the “wiring” underlying biological systems. Using an algorithm that he devised, Alon analyzed the scientific findings existing on networks in some well-researched organisms. He noticed that some patterns in the networks were inexplicably more repetitive than they would be in randomized networks. This handful of patterns was singled out as a potential bundle of design principles.
 
“For a physicist, looking inside the cell is like witnessing a succession of miracles,” says Alon. “The field of physics offered many ‘miracles’ in the past as well – lightning, for instance, evoked an image of Zeus casting a fiery spear. When this belief gave way to an understanding of electric charges, lightning became an ‘interesting phenomenon.’ The basic laws of biology, however, are still unknown, making biology seem ‘miraculous.’ Unearthing these laws is what makes this kind of research so exciting.”
 
Alon’s team has succeeded in uncovering “basic laws” in genetic systems, neural systems and food webs. “Surprisingly, we found two identical laws in genetic and neural systems,” says Alon. “Apparently both information-processing systems employ similar strategies.” Exposing the backbones of such networks can thus help scientists classify systems generically (just as butterflies and ants both belong to the same “class,” neural and genetic systems would also belong to a generic category). This would function as more than just an organizing principle: “One might be able to learn about the neural system by studying the genetic system, which is usually more accessible,” says Alon.
 
In each of seven ecosystems scrutinized, seven recurring patterns relating to food webs were found. One demonstrates that predators will not eat components in the diet of their prey – a lion will eat a gazelle, which eats grass, but it will not eat grass (see below). Humans, who are avid omnivores, are an exception to the rule.
 
Alon’s method detects such patterns – which he calls network motifs – on the basis of their frequency. Any patterns that are functionally important but not statistically significant will not be detected by this method.

“The dream,” says Alon, “is to detect and understand all of the laws governing our bodies, rendering the workings of a cell fully evident and the means of repairing it clear-cut.” Scientists hope that one day in the distant future doctors’ work will be comparable to that of present-day electronic engineers, who analyze blueprints of their subjects and then set to work to put them back in shape.

 
Dr. Uri Alon is the incumbent of the Carl and Frances Korn Career Development Chair in the Life Sciences. His research is supported by the Charpak-Vered Visiting Fellowship, Canada; the Clore Center for Biological Physics; the Rita Markus Foundation Inc.; the Minerva Stiftung Gesellschaft fuer die Forschung m.b.H.; the James and Ilene Nathan Charitable Directed Fund; the Mrs. Harry M. Ringel Memorial Foundation; R.P.H. Promotor Stiftung; the Yad Abraham Center for Cancer Diagnostics and Therapy; and Yad Hanadiv.

Networking Naturally-scientific-1

1. Gene regulation and neural networks: The "feedforward loop." For Z (a gene or a neuron) to be activated, both X and Y must send it a signal (a protein in the case of genes, a pulse in the case of neurons). Y is activated by X, but only when the latter's signal is strong. Thus Z won't begin to be activated when X is present in low concentrations. This motif's function may be to filter noise (low concentrations of X are unimportant noise) and to allow rapid deactivation.

2. Gene regulation networks: Conveyor belt-like activation. X, in relatively small amounts, will produce V. As its amoung increases, it will produce W, Y and Z, respectively. Deactivation will follow the opposite sequence.

Networking Naturally

3. Food webs: Predators don't usually eat the same food as their prey (man-made products like cheese are not taken into account). Omnivores, such as humans, are the exception to the rule and are rare in ecosystems, conformint to the "feedforward loop" shown above.

4. Food webs and neural networks: Different species of prey of a given predator will often have a similar diet. Likewise, if two neurons are activated by the same neuron, they are both likely to be needed to activate a subsequent neuron.
Back (l-r): Students Nadav Kashtan, Ron Milo and Shalev Itzkovitz. Front: Dr. Uri Alon. Nature’s motifs
Math & Computer Science
English

Montezuma's Final Act?

English
Prof. David Mirelman and his research team. Antisense
 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

When the Spaniards conquered Mexico in the early 16th century, they were met with an unexpected form of resistance: life-threatening dysentery, which they called "Montezuma's revenge" (Montezuma being the exalted leader of the Aztecs at that time). Tourists traveling to developing countries sometimes go through the same experience.

 
Today we know that one of the main causes of this disease is an amoeba found in sewage-contaminated drinking water and poorly sanitized food. Amoeba-caused disease claims the lives of thousands yearly and afflicts millions more, mainly in impoverished communities. 
 
Unfortunately, the means to fight amoebic disease remain very limited. Because affected populations usually reside in poor countries pharmaceutical companies do not have sufficient economic incentive to invest in developing new therapies. Now a Weizmann team has succeeded in engineering an amoeba that could become the basis for a pioneering vaccine against amoebic disease.

 

Kiss of Death

 
Amoebas are parasites that settle in the victim's intestine, where they reproduce and attack mucosal cells in the intestines' linings. In the early 1980s Profs. Carlos Gitler and David Mirelman of the Weizmann Institute's Biological Chemistry Department received a joint research grant from the Rockefeller Foundation to study dysentery-causing amoebas. Mirelman focused on lectins, the proteins that enable amoebas to attach themselves to intestinal cells. Gitler, who had immigrated to Israel from Mexico where he personally witnessed amoeba-related suffering, discovered that amoebas kill human cells by injecting a small protein into their membranes. Gitler called this protein an amoebapore; the killing phenomenon was coined "the amoeba kiss of death."  Gitler hoped to produce antibodies that could be used against the amoebapore. However, the anti-bodies proved ineffective because they couldn't reach the amoebapore, which passed directly from the amoebas into the intestinal cells without being exposed.
 
Some 15 years later, technological advances encouraged Mirelman to make an attempt to study the amoebapore's role in the development of disease. Mirelman and team members Rivka Bracha and Yael Nuchamowitz isolated the gene encoding the amoebapore, made a copy of the gene and reversed the orientation of its components (called nucleotides). They then reintroduced the reversed gene (called "anti-sense") into the amoeba, creating an organism that carries both the original ("sense") amoebapore gene and the antisense gene. When the original amoebapore gene starts getting expressed, the anti-sense gene does the same. The resulting two molecules (called messenger RNAs) fit together perfectly, clinging to each other like two sides of a zipper. As a result, neither of the messenger RNA molecules is available for producing the amoebapore protein.
 
illustration of Amoebae protest
 
Using this technique the scientists managed to block some 60% of amoebapore production in the amoebas. The engineered amoebas  were much less aggressive than their original counterparts. Yet the scientists went further: In follow-up research they managed to completely block the gene that encodes the lethal protein, in effect developing a new breed of "silenced" amoebas incapable of making amoebapore and therefore much less harmful to human cells.
 
Now the scientists are trying to see whether the silenced amoebas can be used as a vaccine against aggressive amoebas (similar to the way weakened viruses or bacteria are used as vaccines). If successful, this first vaccination of its kind will open the way to ending the suffering of millions affected by the amoeba parasite.
 
Prof. David Mirelman is the incumbent of the Besen-Brender Chair of Microbiology and Parasitology. His research is supported by the Y. Leon Benoziyo Institute for Molecular Medicine; Erica A. Drake, Scarsdale, NY; Robert Drake, the Netherlands; Mr. and Mrs. Henry Meyer, Wakefield, RI; the M.D. Moross Institute for Cancer Research; and Claire Reich, Forest Hills, NY.
 
 
While attending a conference in China around ten years ago, Mirelman asked local Chinese doctors what they prescribed to patients suffering from intestinal diseases. They told him of an ancient remedy that has been used for almost five thousand years, consisting of an alcohol extract made from freshly crushed garlic cloves. They even jotted down the precise recipe. Surprised to hear that this extract cured patients from the infecting microorganisms without ill effects, Mirelman decided to investigate it. Upon returning to the Weizmann Institute, he prepared the solution and found that a specific molecule, allicin, which is found in fresh garlic extracts, kills amoebas by inactivating some of their crucial enzymes. Though the same molecule can affect enzymes in human cells, they, unlike their amoebic counterparts, are able to reactivate these enzymes. The key to reactivating them lies in a substance called glutathione, which exists in mammalian cells but not in amoebas and most other microorganisms. Efforts to develop therapies for amoebic disease based on these findings are currently under way.
 
 

Prof. Mirelman on the Great Wall of China. Garlic cure

 

 

Prof. David Mirelman and his research team. Antisense
Life Sciences
English

Sperm on the Egghunt

English
 
Left to right: Ph.D. students Anna Gakamsky and Anat Bahat, Prof. Michael Eisenbach. Obstacle course
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Sperm have much in common with the heat-guided missiles used to track down planes and other military targets, a new Weizmann Institute study suggests.
 
The site where the egg lies is slightly warmer than the place where sperm pause during their journey through the female reproductive tract. This temperature difference apparently guides sperm in their navigation. The study, headed by Prof. Michael Eisenbach of the Institute’s Biological Chemistry Department and reported in Nature Medicine, may improve future IVF treatments for couples finding it difficult to conceive.
 
After passing through the womb, sperm cells enter the fallopian tubes. Once inside a tube, they attach themselves to the tube’s wall and pause for “storage,” during which they go through a maturation process that prepares them for penetrating the egg. A sperm cell that has completed this maturation process detaches itself from the wall and leaves the storage site.
If ovulation has taken place in the preceding 24 hours, releasing an egg ready to be fertilized, the mature sperm embarks on a long, complicated journey through the tube to the site of potential fertilization.
Egg and sperm meet in the middle of the fallopian tube
How does the sperm steer a course through the fallopian tube? In earlier studies, Prof. Eisenbach discovered that the egg “calls” the mature sperm by releasing a chemical substance. However, the chemical signal can attract the sperm only across a short range; since the tube normally moves in a wavelike fashion, the chemical apparently cannot spread effectively through the entire tube and therefore cannot signal the sperm over longer distances. This chemical attraction mechanism, known as chemotaxis, cannot therefore explain the sperm’s entire journey.
 

Some like it hot

 

Guided by the knowledge that the sperm storage site is about 2 degrees C cooler than the site of fertilization, Eisenbach and his team – Ph.D. students Anat Bahat and Anna Gakamsky, Dr. Ilan Tur-Kaspa from the Barzilai Medical Center in Ashkelon and visiting Argentinean scientist Dr. Laura C. Giojalas – hypothesized that sperm may be attracted to the fertilization site by a difference in temperature. The technical term for such attraction is thermotaxis.
 
To test this theory, the team built a model of the fertilization process consisting of the sperm storage site, the area where fertilization takes place and the tube in between. They then heated the sperm storage site to a temperature of 37 degrees C (98.6 degrees F) and the fertilization site to the slightly warmer temperature of 39 degrees C (102.2 degrees F), and checked the effect of this setup on the behavior of rabbit sperm. 
 
The findings were clear: The rabbit sperm were indeed sensitive to heat and moved quickly to the warmer fertilization area. On gradually reducing the difference in temperature, the scientists found that even a half-degree difference was enough to attract the sperm. Moreover, they found that only mature sperm – those most likely to penetrate the egg – are heat sensitive.
 
“Apparently, sperm are guided by temperature in their travels through most of the fallopian tube,” says Eisenbach. “Only when they near the fertilization site do they navigate by tuning in to the egg’s chemical call.”
 
The team’s findings were replicated in further research with human sperm, conducted in collaboration with Prof. Haim Breitbart of Bar-Ilan University.
 
Prof. Michael Eisenbach is the incumbent of the Jack and Simon Djanogly Chair of Carbohydrate Biochemistry.
 
 
Left to right: Ph.D. students Anna Gakamsky and Anat Bahat, Prof. Michael Eisenbach. Obstacle course
Life Sciences
English

Riding a Black Hole

English
 
 
The center of our galaxy may well consist of a supermassive black hole – the name given to black holes whose mass is more than one million times that of the sun. Reported in Nature, this finding heralds a new epoch of high-precision black-hole astronomy and might help us better understand how galaxies are born and evolve.
 
Supermassive black holes can be found at the center of many galaxies. The pioneering study, which traced a racing star as it journeyed through the Milky Way, suggests that this may also be true of our galaxy.
 
The massive black holes are thought to develop when many smaller black holes merge at the center of a galaxy and start swallowing everything that comes their way. Such a black hole is a remnant of an exploded sun much bigger than our own. The explosion is a rare celestial phenomenon, called a supernova, which happens when suns use up all their nuclear fuel. The process results in one of the most powerful explosions in nature. Lacking the fuel to maintain the huge pressure required to counter gravity, the star first implodes, and then its outer layers rebound against its core and are violently ejected into space. Simultaneously, the massive core continues to collapse rapidly into itself, forming a black hole.
 
The pull of this dark mass is so great that even light can’t escape it, rendering it invisible. “Invisible _ but not powerless,” says theoretical astrophysicist Dr. Tal Alexander of the Weizmann Institute of Science’s Physics faculty, who participated in the study together with scientists from Germany’s Max Planck Institute for Extraterrestrial Physics and several institutions in France. “The black hole’s presence is felt by its immense gravitational pull. A star that happens to be close to a supermassive black hole will orbit very rapidly around a point of seemingly empty space. Another clue is the radiation emitted by gas heated up just before it is swallowed forever by the black hole.” In a 10-year study, Alexander and his colleagues succeeded in tracking a star known as S2 as it orbited around a known unusual source of radiation (a black-hole candidate called Sagittarius A*) located at the center of our galaxy.
 
The team found that the S2 star does indeed orbit Sagittarius A*; moreover, it picks up speed as it gets closer and closer to its maw, reaching a peak velocity as it whizzes past at 5,000 kilometers (around 3,000 miles) per second. 
 
Some astrophysicists had previously suggested that the dark mass at the center of the Milky Way is not a black hole but, rather, a dense cluster of compact stars or even a giant blob of mysterious subatomic particles.
 
It now appears that these hypotheses are not viable. The new detailed analysis of the orbit, made possible by the techniques developed by the present team, is fully consistent with the view that the dark mass is a supermassive black hole.
 
The observations were made with the new European Very Large Telescope in Chile, whose detectors were developed by scientists from the Max Planck Institute for Extraterrestrial Physics, the Observatoire de Paris, the Office National d’Etudes et de Recherches Aerospatiales and the Observatoire de Grenoble. American scientists participated in the observations.
 
The new techniques allow for precise observation of the center of the galaxy, overcoming the problem of interstellar dust that pervades space. “Such sightings could provide information on a point we know surprisingly little about: our own place in the universe,” Alexander concluded. “We currently do not even know the earth’s exact distance from the center of our own galaxy. Understanding stellar orbits of this kind might tell us where we are.”

 

What a black hole might look like

 

 

White dwarf -- red giant collision near a black hole

 

Dr. Tal Alexander’s research is supported by Sir Harry Djanogly, CBE, London, UK.

 

Stars pulled into the crowded perimeter of a supermassive black hole sometimes collide. Simulation of a collision between two stars.
Space & Physics
English

Mice Grow Human Kidneys

English
 
 Benny Dekel and Prof. Yair Reisner. Hope of a solution
 
More than 50,000 people in the United States alone are on the waiting list for kidney transplants. The wait can last years – and steadily claim victims along the way.
 
A landmark study recently reported in Nature Medicine now offers hope of a future solution. Prof. Yair Reisner of the Weizmann Institute of Science has succeeded in growing miniature human kidneys in mice, using human stem cells. His team has also produced pig kidneys in mice, using the same technique. The kidneys were fully functional.
 
Reisner and Ph.D. student Benny Dekel of the Weizmann Institute’s Immunology Department, with Prof. Justen Passwell, who heads the pediatric department at Tel Aviv’s Sheba Medical Center, transplanted human and pig kidney precursor cells (stem cells destined to become kidney cells) into mice. Both the human and pig tissue grew into perfect mouse-size kidneys. The miniature kidneys were functional, producing urine. In addition, the risk of rejection – a common phenomenon in current transplantation procedures – was greatly reduced, since blood supply within the kidney was provided by host rather than donor blood vessels.
 
“The findings suggest that one day it might be possible to grow a healthy kidney in a human by transplanting human or pig fetal tissue into the patient,” says Reisner. 
 

Window of opportunity

 
To date, the key obstacle to transplanting embryonic stem cells from one kind of animal into another has been that of timing: Cells that were too old suffered substantial immune rejection, while cells that were too young were found to develop into disorganized tissue that included non-kidney structures, such as bone, cartilage and muscle.
 
The Institute team succeeded in pinpointing the ideal time during embryonic development at which stem cells have the best chance of forming well-functioning kidneys with a minimal risk of rejection: 7- to 8-week-old human tissue and 4-week-old porcine tissue were found to offer the optimal window of opportunity for transplantation. Within this time range the tissue lacks certain cells that the body recognizes as foreign.
 
To determine whether the immune system would reject human and pig kidneys grown in mice, the scientists grew the kidneys in mice that lack an immune system. They then restored the animals’ immunity by injecting human immune cells called lymphocytes. Their findings were encouraging: As long as the kidney stem cells were transplanted at the right stage, the lymphocytes did not attack the new pig or human kidneys. Rejection rates in normal (immune-functioning) mice were also reduced compared to those caused by older stem cells. “If all goes well, we hope to begin human trials within a few years,” says Reisner.
 

The challenge of stem cell therapy

 

The current accomplishment of growing functional kidneys in mice using human stem cells marks yet another milestone in the career of Prof. Yair Reisner, whose prize-winning stem cell research has spanned more than 20 years.
 
Stem cells in bone marrow (the sponge-like tissue found in the center of certain bones) are the precursors of red and white blood cells. They play a crucial role in transplant therapies aimed at saving the lives of people with acute leukemia and other blood disorders.
 
The strategy, however, depends on finding a compatible donor. Patients lacking a suitable donor among their siblings have to search the general population, and many fail to find one, even though donor registries – which include more than 8 million volunteers – have been established worldwide.
 
Collaborating with a team led by Prof. Massimo Martelli of Italy’s Perugia University, Reisner has made it possible to transplant even partially matched stem cells in leukemia patients. Nearly 400 patients throughout Europe have been treated using the new approach, yielding significant success rates, as reported in the New England Journal of Medicine, Science and other leading journals. Reisner and Martelli recently received the Daniele Chianelli Prize for their work.
 
The first mismatched transplant using the Reisner-Martelli approach was attempted in 1993, in a 20-year-old factory worker from Italy who had no matched donor in his family. As there was no time to search for an unrelated donor, physicians intended to perform an autologous transplant (using the patient’s own stem cells), but before the transplant was ready, the patient’s disease had progressed to a critical stage. At the family’s request, the Perugia team attempted their new approach, using the patient’s father as a partially matching donor.
 
Following a successful recovery, the patient was able to resume his normal lifestyle and return to his job at the factory, where he still works today.
 
Prof. Yair Reisner is the incumbent of the Henry H. Drake Professorial Chair in Immunology. His research is supported by Richard M. Beleson, San Francisco, CA; Renee Companez, Australia; the Concern Foundation; the Crown Endowment Fund for Immuno-logical Research; Erica A. Drake, Scarsdale, NY; Robert Drake, the Netherlands; the Ligue Nationale Francaise Contre le Cancer; the M.D. Moross Institute for Cancer Research; the Gabrielle Rich Leukemia Research Foundation; Rowland Schaefer, Pembroke Pines, FL; and the Union Bank of Switzerland-Optimus Foundation.
 
Left to right: Ph.D. student Benny Dekel and Prof. Yair Reisner. Timing is everything
Life Sciences
English

Uprooting Hunger in Africa

English

Experimental field has triple yield

 
A slender purple flower is a leading cause of the ever-rising death toll in Africa due to starvation. Appropriately named "witchweed,"it feasts on more than 70 percent of all corn crops in Kenya alone. A recently reported method for killing witchweed may be able to rescue this staple of the African diet from parasitic destruction.

"Witchweed attaches itself to the crop's roots,"says Prof. Jonathan Gressel of the Weizmann Institute of Science's Plant Sciences Department, "then drains it of life." The innovative method of attacking witchweed, conceived by Gressel and developed in collaboration with researchers at CIMMYT (the Spanish acronym for the International Maize and Wheat Improvement Center), kills the colorful weed in its early stages of growth. That is the key to its success.

Until now, African farmers commonly removed witchweed (Striga hermonthica) by hand, but by the time it emerged above ground it had already done its damage. Herbicides applied after its emergence were also ineffective for the same reason.

Gressel decided to test whether coating the corn seeds with herbicide before planting would have an effect. The result: When the seeds sprouted, the parasite unwittingly devoured the weed-killing chemical from the crop's roots or surrounding soil and died. By the time the crop ripened, the herbicide, applied at less than one-tenth the usual rate, had disappeared, leaving the corn unaffected.

Tested in four African countries over ten crop seasons, the technique has on average tripled corn harvests and dramatically cut the cost of growing this crop, sparing farmers the expensive process of air-spraying entire fields. In addition to saving lives, this method may be an economic blessing to Africa: Yields lost to witchweed are valued at approximately $1 billion annually.

For the method to work, the seed itself must be resistant to the herbicides. Gressel sought out strains of corn that resist these herbicides and found one in the United States. His African colleagues Drs. Alpha Diallo and Stephen Mugo crossbred those seeds, provided by Pioneer International, Inc., with local corn to endow them with resistance to other African afflictions as well. The seed treatment technology was perfected by Drs. Fred Kanampiu and Dennis Friesen.

The new technology was presented at a conference in Kenya in July. After viewing the results in the field, Kenyan authorities pledged to fast-track approval for the method.
 
Prof. Gressel's research is supported by the Virginia Polytechnic Institute; Mr. David M. Safer, San Francisco, CA; and the Charles W. and Tillie K. Lubin Center for Plant Biotechnology. He holds the Gilbert de Botton Chair of Plant Sciences.
 
  • According to UN figures, as many as 24,000 people die every day of starvation around the world. This devastation is substantially concentrated in Africa.

  • Since the beginning of 2002, the U.S. Government, by far the leading food donor to Africa, has provided more than $68 million in emergency humanitarian aid and plans to provide an additional $82 million by the year's end.
Kenyan farmer in an experimental corn field
Environment
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Catalyzing Change

English

Profs. David Milstein and Ronny Neumann. Eco-friendly catalysts

One day industry might churn out water instead of waste. This vision -  one of the main goals of a relatively new field called "green chemistry"-  has recently been brought much closer to reality for two key industrial processes.


More than three billion tons of waste are released into the environment each year by the chemical industry in the United States alone. Billions of dollars are then spent every year to comply with laws for the treatment, control, and disposal of waste. Green chemistry, focusing on the prevention of pollutants from the outset, holds that the proverbial ounce of prevention is worth more than a pound of cure. Its aim is to develop new industrial processes that do not generate hazardous substances.

Targeting a major environmental challenge, Profs. David Milstein and Ronny Neumann of the Weizmann Institute's Organic Chemistry Department have cleaned up two processes that work behind the scenes to generate innumerable products ranging from compact discs to pharmaceuticals. The scientists, each working on a different process, designed them so that the only "waste"product is water. Now they are working on adapting the lab-tested methods for industrial use.


Making contact


All around us, as well as within us, molecules interact with one another -  joining, sharing atoms, running off with each other's atoms, or breaking into smaller molecules. For instance, sugar is created when molecules of water and carbon dioxide join. But not all molecules are happy to react with each other -  some are fussy about whom they react with, and some just prefer to be left alone.

The trick behind the design of many products, including plastics and pharmaceuticals, is in causing molecules that normally would take no notice of one another to interact. Many industrial processes employ "mediators"-  mainly chlorine compounds -  that, after making the desired connections, end up as hazardous waste.

Milstein and Neumann, by designing two unique catalysts, have succeeded in causing such molecules to react directly with one another, without mediators.

One process, researched by Milstein's team, is the preparation of substances called aromatic alkenes, which are attractive candidates for the production of key non-steroid anti-inflammatory drugs such as Ibuprofen and Naproxen. Currently they are used for a variety of industrial materials, including plastics. To prepare them, two "unsociable"organic molecules must be merged. The metal catalyst tailored by the team causes the two organic molecules to react directly, without "middlemen,"producing the desired substance with water as the only byproduct (see "The psychol- ogy of atoms"below).

Neumann's team studied the preparation of a substance called propylene oxide (used for a wide range of plastic products), which has an annual market of $5 billion. It is generated by reacting oxygen with propylene, a compound derived from oil or natural gas. Since oxygen rarely reacts with organic materials under normal conditions (and at high temperatures can react with them explosively), Neumann designed a unique metal catalyst to couple oxygen with organic substances directly, cleaning up the process.

The scientists also hope to capitalize on another unique quality of catalysts -  the ability to selectively manipulate, or "reroute,"chemical reactions to produce a desired product. "People often view catalysts as compounds that scurry around in the cell, or in flasks along factory production lines, speeding up a range of chemical reactions. But they're also masters of diversion,"says Neumann. In another of his team's green projects, catalysts are used to stop certain reactions at critical spots, yielding the desired products before waste is generated.

In addition to being environment- friendly, the reactions designed by Milstein and Neumann are much simpler than those currently in use, since they omit many stages of the process. For industry, this could translate into lower production costs. For us, it could translate into safer surroundings and a welcome breath of fresh air.
 

The psychology of atoms


A stable metal is a happy metal. Certain metal atoms, like those of ruthenium, will go to great lengths to achieve happiness. This property is utilized by scientists in making efficient catalysts.

In ruthenium's world, achieving balance means attaining 18 electrons in its "outer shell."Thus it will attract unguarded molecules and bind to them, draining them of electrons. Some caught molecules form partnerships among themselves and take back their electrons, leaving ruthenium to seek out other molecules.

"The 'unhappier'a metal, the more reactive it becomes,"says Milstein. "Ruthenium belongs to a group called 'transition metals,'whose atoms lack electrons and will eagerly react with a variety of molecules to attain them. The metal's 'happiness'depends, however, not only on the number of electrons it gains, but also on whom it takes them from -  in other words, whom it binds with. By understanding what the metal 'wants,'we can design organic groups that induce it to seek out only specific molecules."

Milstein's team attached ruthenium to organic groups of atoms that make it "want"to bind to two specific organic molecules. It seeks each out and binds to it. The organic molecules are thus brought close to one another, in ruthenium's clutches. Displeased with their situation, they strike up a partnership and consequently unite, enabling them to escape ruthenium. The newly formed alliance between the two organic molecules is actually the desired industrial product, "catalyzed"by the tailored ruthenium complex. Later, ruthenium binds to an oxygen molecule that makes off with two hydrogen atoms, forming water.
 

Catalyst credits

 

From plastics to fuels and automobile exhaust systems, from blood clotting to food digestion -  catalysts are crucial to life as we know it. These "hardworking"substances speed up the rate of diverse industrial and biochemical reactions, providing a low-energy shortcut between the reactant and product stages. Essential for nearly all cellular processes, specialized biological catalysts known as enzymes fast-forward reactions that in their absence would occur far too slowly to sustain life. Other catalysts are playing a growing role in worldwide attempts to design greener transportation and streamline factory assembly lines to cut production costs and reduce pollution. Success stories include catalytic converters (based on a metal catalyst), now required in all new cars, which reduce gasoline emissions.
 
Prof. Milstein's research is supported by the Levine Institute of Applied Science and the Helen and Martin Kimmel Center for Molecular Design. He holds the Israel Matz Chair of Organic Chemistry.
Prof. Neumann's research is supported by Yad Hanadiv, Israel; the Helen and Martin Kimmel Center for Molecular Design; the Fritz Haber Center for Physical Chemistry; and Minerva Stiftung Gesellschaft fur die Forschung m.b.H. He holds the Rebecca and Israel Sieff Chair of Organic Chemistry.
 
Profs. David Milstein (left) and Ronny Neumann. Chemistry goes green
Environment
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