泡利不相容原理
肽
水解
水溶液
化学
功能(生物学)
生物物理学
组合化学
生物化学
计算生物学
生物
进化生物学
物理
有机化学
凝聚态物理
作者
Jinyi Yang,Volga Kojasoy,Gerard J. Porter,Ronald T. Raines
出处
期刊:ACS central science
[American Chemical Society]
日期:2024-09-04
卷期号:10 (10): 1829-1834
被引量:7
标识
DOI:10.1021/acscentsci.4c00971
摘要
Proteins have evolved to function in an aqueous environment. Collagen, which provides the bodily scaffold for animals, has a special need to retain its integrity. This need was addressed early on, as intact collagen has been detected in dinosaur fossils, even though peptide bonds have a half-life of only ∼500 years in a neutral aqueous solution. We sought to discover the physicochemical basis for this remarkable resistance to hydrolysis. Using experimental and computational methods, we found that a main-chain acyl group can be protected from hydrolysis by an O···C=O n→π* interaction with a neighboring acyl group. These interactions engage virtually every peptide bond in a collagen triple helix. This protection, which arises from the Pauli exclusion principle, could underlie the preservation of ancient collagen.
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