3FQ9

Design of an insulin analog with enhanced receptor-binding selectivity. Rationale, structure, and therapeutic implications

3FQ9 の概要

• エントリーDOI: 10.2210/pdb3fq9/pdb
• 関連するPDBエントリー: 4INS
• 分子名称: Insulin, ZINC ION, ... (4 entities in total)
• 機能のキーワード: receptor-binding, insulin design, rational, therapeutic implication, carbohydrate metabolism, cleavage on pair of basic residues, diabetes mellitus, disease mutation, glucose metabolism, hormone, pharmaceutical, secreted
• 細胞内の位置: Secreted: P01308 P01308
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 11792.20

構造登録者

Zhao, M.,Wan, Z.L.,Whittaker, L.,Xu, B.,Phillips, N.,Katsoyannis, P.,Whittaker, J.,Weiss, M.A. (登録日: 2009-01-07, 公開日: 2009-08-04, 最終更新日: 2023-09-06)

主引用文献

Zhao, M.,Wan, Z.L.,Whittaker, L.,Xu, B.,Phillips, N.B.,Katsoyannis, P.G.,Ismail-Beigi, F.,Whittaker, J.,Weiss, M.A.
Design of an insulin analog with enhanced receptor binding selectivity: rationale, structure, and therapeutic implications.
J.Biol.Chem., 284:32178-32187, 2009

PubMed Abstract: Insulin binds with high affinity to the insulin receptor (IR) and with low affinity to the type 1 insulin-like growth factor (IGF) receptor (IGFR). Such cross-binding, which reflects homologies within the insulin-IGF signaling system, is of clinical interest in relation to the association between hyperinsulinemia and colorectal cancer. Here, we employ nonstandard mutagenesis to design an insulin analog with enhanced affinity for the IR but reduced affinity for the IGFR. Unnatural amino acids were introduced by chemical synthesis at the N- and C-capping positions of a recognition alpha-helix (residues A1 and A8). These sites adjoin the hormone-receptor interface as indicated by photocross-linking studies. Specificity is enhanced more than 3-fold on the following: (i) substitution of Gly(A1) by D-Ala or D-Leu, and (ii) substitution of Thr(A8) by diaminobutyric acid (Dab). The crystal structure of [D-Ala(A1),Dab(A8)]insulin, as determined within a T(6) zinc hexamer to a resolution of 1.35 A, is essentially identical to that of human insulin. The nonstandard side chains project into solvent at the edge of a conserved receptor-binding surface shared by insulin and IGF-I. Our results demonstrate that modifications at this edge discriminate between IR and IGFR. Because hyperinsulinemia is typically characterized by a 3-fold increase in integrated postprandial insulin concentrations, we envisage that such insulin analogs may facilitate studies of the initiation and progression of cancer in animal models. Future development of clinical analogs lacking significant IGFR cross-binding may enhance the safety of insulin replacement therapy in patients with type 2 diabetes mellitus at increased risk of colorectal cancer.

PubMed: 19773552
DOI: 10.1074/jbc.M109.028399

実験手法

X-RAY DIFFRACTION (1.35 Å)