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序列选择性保护肽免受蛋白水解。

Sequence-Selective Protection of Peptides from Proteolysis.

机构信息

Department of Chemistry, Iowa State University, Ames, IA, 50011-3111, USA.

出版信息

Angew Chem Int Ed Engl. 2021 May 10;60(20):11092-11097. doi: 10.1002/anie.202102148. Epub 2021 Mar 30.

Abstract

Proteolysis of proteins and peptides is involved in the infection of cells by enveloped viruses and also in the invasion and spread of cancer cells. Shutting down broad-specificity proteases, however, is problematic because normal functions by these proteases will be affected. Herein, nanoparticle receptors were prepared from molecular imprinting for complex biological peptides. Their strong and selective binding enabled them to protect their targeted sequences from proteolysis in aqueous solution at stoichiometric amounts. Generality of the method was demonstrated by the protection of hydrophobic and hydrophilic peptides from different proteases, selective protection of a segment of a long peptide, and selective protection of a targeted peptide in a mixture. Most interestingly, two receptors targeting different parts of a long peptide could work in cooperation to protect the overall sequence, highlighting the versatility of the method.

摘要

蛋白质和肽的蛋白水解参与包膜病毒感染细胞,也参与癌细胞的侵袭和扩散。然而,广泛特异性蛋白酶的失活存在问题,因为这些蛋白酶的正常功能将受到影响。在此,通过分子印迹制备了用于复杂生物肽的纳米颗粒受体。它们的强特异性结合使它们能够以化学计量的量在水溶液中保护其靶向序列免受蛋白水解。该方法的通用性通过保护来自不同蛋白酶的疏水性和亲水性肽、选择性保护长肽的一段以及在混合物中选择性保护靶向肽得到证明。最有趣的是,针对长肽不同部分的两个受体可以协同工作以保护整个序列,突出了该方法的多功能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f5e/8252432/cbc443c78cc6/ANIE-60-11092-g002.jpg

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