While scientists have identified proteins that drive myriad diseases, finding ways to control them is another matter. Thanks to structural and chemical limitations, only 20 percent of the body’s proteins can be targeted with existing drugs. Most existing pharmaceuticals are either small molecules that require very specific surface features to enter a cell or large biological molecules that are too big to gain entry. But new types of therapeutic molecules developed over the last decade, called stapled peptides, may be able to work their way into tissues that were previously inaccessible. In research presented at the American Chemical Society meeting in California last week, Harvard biochemist Gregory Verdine described two potential new drugs—one for colon cancer and one for asthma—that are capable of going where none have gone before.
“The world of biology has rocketed ahead to explain the proteins that cause disease, but the world of targeting and chemistry has not kept pace,” Verdine says. “What we need are new types of molecules that are able to gain access to the inside of cells and that have the kind of surface properties that allow them to target things that small molecules can’t.”
The most successful of today’s therapies work by interacting with receptors on a cell’s surface, or by using small molecules that can enter a cell via water-phobic “greasy” pockets. The problem, however, occurs when cells lack the necessary surface features. For example, proteins responsible for tumor cell growth have been difficult to inhibit via traditional means. To solve the problem, Verdine turned to short pieces of protein called peptides, which can switch disease pathways within the cell on or off and can also be manipulated into shapes that slip easily into a cell’s nucleus.
The idea of manipulating peptides into therapeutics is not new, but the problem has been that they’re notoriously unstable. They tend to lose their shape once isolated from their parent protein and are rapidly broken down by the body’s enzymes. Verdine and his collaborators have gotten around this problem by folding a peptide into shape and holding it there by strategically placing two amino acids on the peptide and linking them together into a chemical “staple.” The result is a strong, stable, helical peptide that can penetrate a cell’s interior and retain its shape long enough to have therapeutic effects.
Verdine has since built a few different peptides that target disease pathways. The latest example could be a boon for cancer biology. It targets a protein called beta-catenin that is important for embryonic growth and development but can cause cancer–most commonly, colon cancer–when its production goes unchecked. Using the stapling approach, Verdine and his colleagues have developed a peptide that can move through cell membranes and directly target beta-catenin production at the DNA level. Tests in cell culture have been promising, and the group is about to begin animal studies.
“While it’s been known for many years that beta-catenin is a major player in several human cancers, it’s been impossible to attack it using traditional chemistry approaches,” says Frank McCormick, a cancer biologist and director of the Helen Diller Family Comprehensive Cancer Center at the University of California at San Francisco. “It’s on the list of proteins that the whole field would like to develop targets against but that, so far, have proven undruggable. It’s potentially a really big step forward.”
The second target Verdine and his colleagues attacked, interleukin 13, has been linked to the development of asthma. The resulting stapled peptide, three years in the making and still in early development, could help treat the underlying cause of disease with a drug that, due to its stapled formation, could be stable without refrigeration.
Verdine cofounded Aileron Therapeutics in 2005 to commercialize the stapled-peptide technology, and the company has since tested its peptides in multiple animal models of cancer. According to Verdine, Aileron plans to start its first human trials sometime next year.
“It’s a very attractive approach,” says McCormick. “The next step will be seeing if these drugs will make it all the way through to the clinic. We’ll be watching closely and with optimism.”
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