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桥连肽大环化合物作为PDZ结构域蛋白的配体

Bridged peptide macrocycles as ligands for PDZ domain proteins.

作者信息

Udugamasooriya Gomika, Saro Dorina, Spaller Mark R

机构信息

Department of Chemistry, Wayne State University, Detroit, Michigan 48202, USA.

出版信息

Org Lett. 2005 Mar 31;7(7):1203-6. doi: 10.1021/ol0475966.

Abstract

[reaction: see text] Conformationally constrained side chain-bridged cyclic peptides were prepared using bis-carboxylic acid ring spacers. These macrocyles were designed to inhibit protein-protein interactions mediated by the third PDZ domain (PDZ3) of a mammalian neuronal protein, PSD-95. Isothermal titration calorimetry (ITC) experiments measured dissociation constants in the low micromolar range. For each compound, the change in entropy (TdeltaS) of binding either is comparable in magnitude to the enthalpy change (deltaH) or is the predominant driving force for association.

摘要

[反应:见正文] 使用双羧酸环间隔基制备了构象受限的侧链桥连环肽。这些大环化合物旨在抑制由哺乳动物神经元蛋白PSD - 95的第三个PDZ结构域(PDZ3)介导的蛋白质 - 蛋白质相互作用。等温滴定量热法(ITC)实验测量的解离常数在低微摩尔范围内。对于每种化合物,结合时的熵变(TΔS)在大小上与焓变(ΔH)相当,或者是缔合的主要驱动力。

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