The 2018 Nobel Prize in chemistry was awarded Wednesday morning to three scientists who put evolution to work to design molecules from living organisms that eventually led to the development of cleaner biofuels and drugs for treating diseases including psoriasis.
Half of the $1 million prize went to Frances Arnold, 62, at the California Institute of Technology, the fifth woman ever to receive the Nobel Prize in chemistry. The remainder was divided between George Smith, 77, at the University of Missouri Columbia and Gregory Winter, 67, at the MRC Laboratory of Molecular Biology in the United Kingdom.
Humans have been tinkering with other species since at least the dawn of civilization, from domesticating dogs to breeding more productive crops. But what the 2018 Nobel chemistry laureates figured out was how to use those same principles of selectively reproducing desired traits to make specific molecules, namely enzymes and antibodies.
Arnold tackled enzymes. These are proteins that serve as catalysts, speeding up chemical reactions without being used up in the process. In nature, enzymes do things like break apart long starch chains into sugars, assemble proteins, or transcribe DNA.
But suppose you want an enzyme to do something slightly different, say turn a starchy plant like corn into a clean-burning biofuel. The requires tuning biological machinery from a bacterium or fungus with a technique known as directed evolution to break down the corn in a new way.
Directed evolution is an iterative process scientists use to design biological molecules like enzymes. It requires inducing some randomness in the target enzyme within an organism like bacteria. The resulting mutated bacteria are screened to see which ones perform the intended function the best. The winners are then cultured, and from their offspring, the best are selected, and then cultured, and so on.
Essentially, it’s the same selective breeding process humans have used for thousands of years to develop better crops, just accelerated in the lab.
In 1993, Arnold reported that she used this technique to produce an enzyme that could still work well even when treated with a chemical that would otherwise drastically weaken the natural enzyme. This bit of “unnatural selection” was an important validation of directed evolution. It showed how scientists could use nature’s molecular tools to serve humanity’s needs.
Arnold’s methods are now used to produce pharmaceuticals, specialty chemicals, and enzymes for biofuels.
Smith and Winter meanwhile worked with a technique called phage display. It’s a process where you use a virus that can infect bacteria, known as a bacteriophage, to generate new proteins. In a series of papers in the 1980s, Smith figured out that the bacteriophage displays certain proteins on its surface, making it easier to screen variants. He also found that he could alter those surface proteins and make copies of a desired molecule.
Winter then coupled the phage display technique with directed evolution to produce new antibodies for the immune system to identify threats. He reported his results in 1990. In 2002, the first therapy using evolved antibodies was approved and is now used to treat psoriasis, rheumatoid arthritis, and inflammatory bowel disease.
The Nobel Committee noted in its announcement that these techniques are still new and we have not yet seen their full potential to fight disease or create new fuels. “We are in the early days of directed evolution’s revolution which, in many different ways, is bringing and will bring the greatest benefit to humankind,” the committee wrote.
Sourse: vox.com
