
Peptides have found use in over 80 drugs worldwide since insulin was first synthesized in the 1920s.
Image Credit: Scientific Frontline
Scientific Frontline: "At a Glance" Summary
- Main Discovery: Researchers at UC Santa Barbara developed an efficient technique to synthesize non-natural amino acids that are immediately ready for direct use in peptide construction without extra modification steps.
- Methodology: The team utilized gold catalysis to generate stereoselective amino acids from inexpensive chemical ingredients, subsequently assembling them into peptides through a rinse-and-repeat process on a resin scaffold.
- Key Data: While lifeforms naturally utilize only 22 amino acids to build proteins, this breakthrough expands the available biochemical toolkit from a limited 22-molecule palette to potentially hundreds of noncanonical variations.
- Significance: The ability to easily incorporate non-natural amino acids allows drug designers to armor-plate peptide therapeutics against destructive bodily enzymes and force them into specific shapes for superior receptor binding.
- Future Application: Researchers plan to automate the synthesis process to provide non-chemists in drug development and materials research with accessible, low-friction access to these expanded molecular building blocks.
- Branch of Science: Biochemistry, Pharmacology, and Materials Science.
- Additional Detail: Unlike existing approaches that require complex manipulation, this method produces amino acids where the acid group is already primed to react, leaving only the amino group requiring unmasking.
.jpg)
.jpg)

.jpg)

.jpg)





.jpg)


.jpg)

.jpg)

.jpg)