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巴纳酶-巴塔林对:在癌症研究和纳米技术中的当代应用。

Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology.

机构信息

Shemyakin & Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia.

Center of Biomedical Engineering, Sechenov University, 119991 Moscow, Russia.

出版信息

Molecules. 2021 Nov 10;26(22):6785. doi: 10.3390/molecules26226785.

Abstract

Barnase is an extracellular ribonuclease secreted by that was originally studied as a small stable enzyme with robust folding. The identification of barnase intracellular inhibitor barstar led to the discovery of an incredibly strong protein-protein interaction. Together, barnase and barstar provide a fully genetically encoded toxin-antitoxin pair having an extremely low dissociation constant. Moreover, compared to other dimerization systems, the barnase-barstar module provides the exact one-to-one ratio of the complex components and possesses high stability of each component in a complex and high solubility in aqueous solutions without self-aggregation. The unique properties of barnase and barstar allow the application of this pair for the engineering of different variants of targeted anticancer compounds and cytotoxic supramolecular complexes. Using barnase in suicide gene therapy has also found its niche in anticancer therapy. The application of barnase and barstar in contemporary experimental cancer therapy is reflected in the review.

摘要

Barnase 是一种由 分泌的细胞外核糖核酸酶,最初被研究为一种具有稳健折叠的小型稳定酶。 Barnase 细胞内抑制剂 barstar 的鉴定导致了一种非常强的蛋白质-蛋白质相互作用的发现。 Barnase 和 barstar 一起提供了一个完全遗传编码的毒素-抗毒素对,具有极低的解离常数。此外,与其他二聚化系统相比, barnase-barstar 模块提供了复合物成分的确切一一对应比例,并且在复合物中每个成分具有高稳定性和在水溶液中的高溶解度而没有自聚集。 Barnase 和 barstar 的独特性质允许将该对用于工程化不同靶向抗癌化合物和细胞毒性超分子复合物的变体。 在自杀基因治疗中使用 barnase 也在抗癌治疗中找到了其位置。 Barnase 和 barstar 在当代实验性癌症治疗中的应用在综述中得到了反映。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fd7/8625414/096532b24dfd/molecules-26-06785-g001.jpg

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