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解读聚糖密码:分子动力学和量子化学揭示O-聚糖官能团如何在嗜黏蛋白阿克曼氏菌降解黏蛋白过程中调控OgpA的选择性。

Unravelling the Glycan Code: Molecular Dynamics and Quantum Chemistry Reveal How O-Glycan Functional Groups Govern OgpA Selectivity in Mucin Degradation by Akkermansia muciniphila.

作者信息

Khavani Mohammad, Mehranfar Aliyeh, Mofrad Mohammad R K

机构信息

Molecular Cell Biomechanics Laboratory, Department of Bioengineering and Mechanical Engineering, University of California Berkeley, Berkeley, California, USA.

Molecular Biophysics and Integrative Bioimaging Division, Lawrence Berkeley National Lab, Berkeley, CA, USA.

出版信息

Microb Biotechnol. 2025 Apr;18(4):e70091. doi: 10.1111/1751-7915.70091.

Abstract

Mucins, heavily O-glycosylated glycoproteins, are a key component of mucus, and certain gut microbiota, including Akkermansia muciniphila, can utilise mucin glycans as a carbon source. Akkermansia muciniphila produces the O-glycopeptidase enzyme OgpA, which cleaves peptide bonds at the N-terminus of serine (Ser) or threonine (Thr) residues carrying O-glycan substitutions, with selectivity influenced by the O-glycan functional groups. Using molecular dynamics (MD) simulations and quantum chemistry calculations, we explored how different O-glycan groups affect OgpA's selectivity. Our results show that peptides bind to the enzyme via hydrogen bonds, π-π interactions, van der Waals forces and electrostatic interactions, with key residues, including Tyr90, Val138, Gly176, Tyr210 and Glu91, playing important roles. The primary determinant of selectivity is the interaction between the peptide's functional group and the enzyme's binding cavity, while peptide-enzyme interface interactions are secondary. Quantum chemistry calculations reveal that OgpA prefers peptides with a lower electrophilic character. This study provides new insights into mucin degradation by gut microbiota enzymes, advancing our understanding of this critical biological process.

摘要

粘蛋白是高度O-糖基化的糖蛋白,是黏液的关键组成部分,某些肠道微生物群,包括嗜黏蛋白阿克曼氏菌,能够利用粘蛋白聚糖作为碳源。嗜黏蛋白阿克曼氏菌产生O-糖肽酶OgpA,该酶可切割携带O-聚糖取代基的丝氨酸(Ser)或苏氨酸(Thr)残基N端的肽键,其选择性受O-聚糖官能团影响。利用分子动力学(MD)模拟和量子化学计算,我们探究了不同的O-聚糖基团如何影响OgpA的选择性。我们的结果表明,肽通过氢键、π-π相互作用、范德华力和静电相互作用与酶结合,包括Tyr90、Val138、Gly176、Tyr210和Glu91在内的关键残基发挥着重要作用。选择性的主要决定因素是肽的官能团与酶结合腔之间的相互作用,而肽-酶界面相互作用是次要的。量子化学计算表明,OgpA更喜欢亲电特性较低的肽。这项研究为肠道微生物群酶对粘蛋白的降解提供了新的见解,增进了我们对这一关键生物学过程的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5618/11968330/88a70613eabe/MBT2-18-e70091-g004.jpg

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