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肺炎链球菌神经氨酸酶 NanA、NanB 和 NanC 的催化途径比较研究。

Comparative studies of catalytic pathways for Streptococcus pneumoniae sialidases NanA, NanB and NanC.

机构信息

School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW, 2500, Australia.

Molecular Horizons, University of Wollongong, Wollongong, NSW, 2500, Australia.

出版信息

Sci Rep. 2019 Feb 15;9(1):2157. doi: 10.1038/s41598-018-38131-z.

Abstract

Streptococcus pneumoniae (S. pneumoniae) is a leading human pathogen, which takes large responsibility for severe otitis media, acute meningitis and septicaemia. It encodes up to three distinct sialidases: NanA, NanB and NanC, which are promising drug targets. Recent experimental studies have shown that these three sialidases might work together up to the ultimate step, where NanA and NanB produce N-acetylneuraminic acid (Neu5Ac) and 2,7-anhydro-Neu5Ac following the functions of sialidase and intramolecular trans-sialidase, whilst NanC carries on a ping-pong mechanism that produces or removes 2-deoxy-2,3-didehydro-Neu5AC. It is intriguing that these sialidases have similar active sites but operate via three distinct reaction pathways. To clarify this issue, herein we present the first systematic computational investigation on the catalytic pathways for S. pneumoniae NanA, NanB and NanC based on combined quantum mechanics/molecular mechanics simulations, and propose the most preferred routes for the three S. pneumoniae sialidases. Our findings support the mechanisms of NanA and NanC that were proposed by previous experimental studies, whereas the role of water in NanB was found to differ slightly from our current understandings. The mechanistic insights obtained from this work are expected to assist in the design of potent inhibitors targeting these key enzymes for therapeutic applications.

摘要

肺炎链球菌(S. pneumoniae)是一种主要的人类病原体,它是严重中耳炎、急性脑膜炎和败血症的主要致病因素。它编码多达三种不同的唾液酸酶:NanA、NanB 和 NanC,它们是有前途的药物靶点。最近的实验研究表明,这三种唾液酸酶可能共同作用于最终步骤,其中 NanA 和 NanB 在唾液酸酶和分子内转唾液酸酶的作用下产生 N-乙酰神经氨酸(Neu5Ac)和 2,7-脱水-Neu5Ac,而 NanC 通过乒乓机制产生或去除 2-脱氧-2,3-二脱氢-Neu5AC。有趣的是,这些唾液酸酶具有相似的活性位点,但通过三种不同的反应途径发挥作用。为了解决这个问题,我们在此基于量子力学/分子力学模拟对 S. pneumoniae NanA、NanB 和 NanC 的催化途径进行了首次系统的计算研究,并提出了三种 S. pneumoniae 唾液酸酶的最优选途径。我们的研究结果支持了先前实验研究提出的 NanA 和 NanC 的机制,而发现 NanB 中的水的作用与我们目前的理解略有不同。这项工作获得的机制见解有望有助于设计针对这些关键酶的有效抑制剂,以用于治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215a/6377674/401c39e19951/41598_2018_38131_Fig1_HTML.jpg

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