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一个扭结蛋白的转位动力学中的马库斯型反转区域。

A Marcus-Type Inverted Region in the Translocation Kinetics of a Knotted Protein.

机构信息

Department of Chemistry, Indian Institute of Technology (Banaras Hindu University), Varanasi, Uttar Pradesh 221005, India.

Department of Physics, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.

出版信息

J Phys Chem Lett. 2023 Nov 30;14(47):10719-10726. doi: 10.1021/acs.jpclett.3c02183. Epub 2023 Nov 27.

Abstract

Knotted proteins are rare but important species, yet how their complex topologies affect their physical properties is not fully understood. Here we combine single molecule nanopore experiments and all-atom MD simulations to study the electric-field-driven unfolding during the translocation through a model pore of individual protein knots important for methylating tRNA. One of these knots shows an unusual behavior that resembles the behavior of electrons hopping between two potential surfaces: as the electric potential driving the translocation reaction is increased, the rate eventually plateaus or slows back down in the "Marcus inverted regime". Our results shed light on the influence of topology in knotted proteins on their forced translocation through a pore connecting two electrostatic potential wells.

摘要

纽结蛋白虽然罕见,但却很重要,然而,其复杂的拓扑结构如何影响它们的物理性质还不完全清楚。在这里,我们结合单分子纳米孔实验和全原子 MD 模拟来研究单个蛋白纽结在穿过模型孔时的电场驱动解折叠过程,这些蛋白纽结对于甲基化 tRNA 很重要。其中一个纽结表现出一种不寻常的行为,类似于电子在两个势能表面之间跳跃的行为:随着驱动易位反应的电场增加,速率最终在“马库斯反转区”中达到平台或减缓。我们的结果阐明了拓扑结构对连接两个静电势阱的孔中强制易位的纽结蛋白的影响。

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