A ribosome reads an mRNA sequence and produces protein according to its genetic code.
From left, Venkatraman Ramakrishnan of the MRC Laboratory of Molecular Biology in Cambridge, England; Thomas A. Steitz of Yale University; and Ada E. Yonath of the Weizmann Institute of Science in Rehovot, Israel will share the 2009 Nobel Prize in Chemistry.
"Ribosomes are key to life," Malcolm Ritter of The Associated Press explained: "They use instructions from genes to make thousands of different proteins that control what happens in the body. Many antibiotics kill bacteria by attacking their ribosomes, and the detailed descriptions by new Nobelists are being used to develop new drugs."
"The chemistry prize was awarded for research into how information on strands of DNA is translated into proteins."
"Ribosomes were discovered in the 1950’s by George Palade, who went on to win the Nobel Prize in Physiology or Medicine for his work on the makeup of cells, but scientists weren’t able to take a close look at those organelles till the end of the century. Thomas Steitz, Venkatraman Ramakrishnan, and Ada Yonath developed tricks for examining the tiny structures with x-rays and electron beams. The high-resolution 3D images they acquired will help chemists develop a host of better medications."
"Dozens of antibiotics — including tetracycline and clindamycin — work by gumming up the ribosomes inside bacteria. Each of those medications is made up of relatively small molecules that can wedge themselves into crevices in the ribosome, destroying the microbes’ ability to make protein, and thus rendering them helpless.
"Armed with 3D images of antibiotic molecules wedged into ribosomes, medicinal chemists can refine their strategy for fighting bacteria. They can find new weak spots in bacterial ribosomes.
"That approach is a lot like the way that the Rebel Alliance destroyed the first Death Star: by looking at its blueprint and finding a weak spot. Except, in this case the researchers are looking for vulnerable nooks and crannies in a blob of RNA and protein, rather than a thermal exhaust port.
"Dozens of 3D images that show antibiotics sticking to ribosomes are available in the Protein DataBank, and you can look at them yourself with a tool called First Glance.
"Just type the Protein DataBank ID number for the ribosome that you want to look at, and then start exploring.
"Here are some of the best structures:
Ribosome with Clindamycin: 1YJN
Ribosome with Azithromycin: 1NWY
Ribosome with Erythromycin: 1JZY"
"Armed with 3D images of antibiotic molecules wedged into ribosomes, medicinal chemists can refine their strategy for fighting bacteria. They can find new weak spots in bacterial ribosomes.
"That approach is a lot like the way that the Rebel Alliance destroyed the first Death Star: by looking at its blueprint and finding a weak spot. Except, in this case the researchers are looking for vulnerable nooks and crannies in a blob of RNA and protein, rather than a thermal exhaust port.
"Dozens of 3D images that show antibiotics sticking to ribosomes are available in the Protein DataBank, and you can look at them yourself with a tool called First Glance.
"Just type the Protein DataBank ID number for the ribosome that you want to look at, and then start exploring.
"Here are some of the best structures:
Ribosome with Clindamycin: 1YJN
Ribosome with Azithromycin: 1NWY
Ribosome with Erythromycin: 1JZY"
Following the announcement, Professor Gunnar von Heijne told senior editor Simon Frantz how the achievements awarded the 2009 Nobel Prize in Chemistry not only provided insights into life at the atomic level, but also provided insights into how to save lives.
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