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通过定制纳米颗粒支架的表面识别来控制蛋白质结构和功能。

Control of protein structure and function through surface recognition by tailored nanoparticle scaffolds.

作者信息

Hong Rui, Fischer Nicholas O, Verma Ayush, Goodman Catherine M, Emrick Todd, Rotello Vincent M

机构信息

Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA.

出版信息

J Am Chem Soc. 2004 Jan 28;126(3):739-43. doi: 10.1021/ja037470o.

DOI:10.1021/ja037470o
PMID:14733547
Abstract

Thioalkyl and thioalkylated oligo(ethylene glycol) (OEG) ligands with chain-end functionality were used to fabricate water-soluble CdSe nanoparticle scaffolds. Surface recognition of chymotrypsin (ChT) was achieved using these functionalized nanoparticle scaffolds, with three levels of interaction demonstrated: no interaction (OEG terminated with hydroxyl group), inhibition with denaturation (carboxylate-terminated thioalkyl ligands), and inhibition with retention of structure (carboxylate-terminated OEG). The latter process was reversible upon an increase in ionic strength, with essentially complete restoration of enzymatic activity.

摘要

具有链端功能的硫代烷基和硫代烷基化聚乙二醇(OEG)配体被用于制备水溶性CdSe纳米颗粒支架。利用这些功能化纳米颗粒支架实现了对胰凝乳蛋白酶(ChT)的表面识别,展示了三种相互作用水平:无相互作用(羟基封端的OEG)、变性抑制(羧基封端的硫代烷基配体)以及结构保留抑制(羧基封端的OEG)。后一过程在离子强度增加时是可逆的,酶活性基本完全恢复。

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