5HPU

Insulin with proline analog HyP at position B28 in the R6 state

5HPU の概要

• エントリーDOI: 10.2210/pdb5hpu/pdb
• 関連するPDBエントリー: 5HPR
• 分子名称: Insulin, chain A, Insulin, chain B, PHENOL, ... (6 entities in total)
• 機能のキーワード: insulin, non-canonical amino acid, hydroxyproline, non-natural amino acid, unnatural amino acid, hormone
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 12057.25

構造登録者

Lieblich, S.A.,Fang, K.Y.,Cahn, J.K.B.,Tirrell, D.A. (登録日: 2016-01-21, 公開日: 2017-01-25, 最終更新日: 2023-09-27)

主引用文献

Lieblich, S.A.,Fang, K.Y.,Cahn, J.K.B.,Rawson, J.,LeBon, J.,Ku, H.T.,Tirrell, D.A.
4S-Hydroxylation of Insulin at ProB28 Accelerates Hexamer Dissociation and Delays Fibrillation.
J. Am. Chem. Soc., 139:8384-8387, 2017

PubMed Abstract: Daily injections of insulin provide lifesaving benefits to millions of diabetics. But currently available prandial insulins are suboptimal: The onset of action is delayed by slow dissociation of the insulin hexamer in the subcutaneous space, and insulin forms amyloid fibrils upon storage in solution. Here we show, through the use of noncanonical amino acid mutagenesis, that replacement of the proline residue at position 28 of the insulin B-chain (ProB28) by (4S)-hydroxyproline (Hzp) yields an active form of insulin that dissociates more rapidly, and fibrillates more slowly, than the wild-type protein. Crystal structures of dimeric and hexameric insulin preparations suggest that a hydrogen bond between the hydroxyl group of Hzp and a backbone amide carbonyl positioned across the dimer interface may be responsible for the altered behavior. The effects of hydroxylation are stereospecific; replacement of ProB28 by (4R)-hydroxyproline (Hyp) causes little change in the rates of fibrillation and hexamer disassociation. These results demonstrate a new approach that fuses the concepts of medicinal chemistry and protein design, and paves the way to further engineering of insulin and other therapeutic proteins.

PubMed: 28598606
DOI: 10.1021/jacs.7b00794

実験手法

X-RAY DIFFRACTION (2.2 Å)