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蛋白-Fucosyltransferase 1 在溶液中经历结构域间的柔韧性变化。

Protein -Fucosyltransferase 1 Undergoes Interdomain Flexibility in Solution.

机构信息

Institute of Biocomputation and Physics of Complex Systems (BIFI), University of Zaragoza, 50018 Zaragoza, Spain.

Instituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, 50009 Zaragoza, Spain.

出版信息

Molecules. 2021 Apr 7;26(8):2105. doi: 10.3390/molecules26082105.

Abstract

Protein -fucosyltransferase 1 (PoFUT1) is a GT-B fold enzyme that fucosylates proteins containing EGF-like repeats. GT-B glycosyltransferases have shown a remarkable grade of plasticity adopting closed and open conformations as a way of tuning their catalytic cycle, a feature that has not been observed for PoFUT1. Here, we analyzed PoFUT1 (PoFUT1) conformational behavior in solution by atomic force microscopy (AFM) and single-molecule fluorescence resonance energy transfer (SMF-FRET). Our results show that this enzyme is very flexible and adopts mainly compact conformations and to a lesser extend a highly dynamic population that oscillates between compact and highly extended conformations. Overall, our experiments illustrate the inherent complexity of PoFUT1 dynamics, which might play a role during its catalytic cycle.

摘要

蛋白岩藻糖基转移酶 1(PoFUT1)是一种 GT-B 折叠酶,能够对含有表皮生长因子样重复序列的蛋白进行岩藻糖基化修饰。GT-B 糖基转移酶已经表现出显著的可塑性,能够通过采用闭合和开放构象来调节其催化循环,而这种特性在 PoFUT1 中尚未观察到。在这里,我们通过原子力显微镜(AFM)和单分子荧光共振能量转移(SMF-FRET)分析了 PoFUT1 在溶液中的构象行为。我们的结果表明,这种酶非常灵活,主要采用紧凑的构象,并且在较小程度上采用高度动态的种群,该种群在紧凑和高度扩展的构象之间振荡。总体而言,我们的实验说明了 PoFUT1 动力学的固有复杂性,这可能在其催化循环中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15bd/8067585/8c58fdd3b28f/molecules-26-02105-g001.jpg

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