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螺旋结构和动力学在寡聚腺苷酸合成酶 1(OAS1)对短双链 RNA 的错配容忍和激活中的作用。

Role of helical structure and dynamics in oligoadenylate synthetase 1 (OAS1) mismatch tolerance and activation by short dsRNAs.

机构信息

Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322.

Graduate Program in Biochemistry, Cell and Developmental Biology, Graduate Division of Biological and Biomedical Sciences, Emory University, Atlanta, GA 30322.

出版信息

Proc Natl Acad Sci U S A. 2022 Jan 18;119(3). doi: 10.1073/pnas.2107111119.

Abstract

The 2'-5'-oligoadenylate synthetases (OAS) are innate immune sensors of cytosolic double-stranded RNA (dsRNA) that play a critical role in limiting viral infection. How these proteins are able to avoid aberrant activation by cellular RNAs is not fully understood, but adenosine-to-inosine (A-to-I) editing has been proposed to limit accumulation of endogenous RNAs that might otherwise cause stimulation of the OAS/RNase L pathway. Here, we aim to uncover whether and how such sequence modifications can restrict the ability of short, defined dsRNAs to activate the single-domain form of OAS, OAS1. Unexpectedly, we find that all tested inosine-containing dsRNAs have an increased capacity to activate OAS1, whether in a destabilizing (I•U) or standard Watson-Crick-like base pairing (I-C) context. Additional variants with strongly destabilizing A•C mismatches or stabilizing G-C pairs also exhibit increased capacity to activate OAS1, eliminating helical stability as a factor in the relative ability of the dsRNAs to activate OAS1. Using thermal difference spectra and molecular dynamics simulations, we identify both increased helical dynamics and specific local changes in helical structure as important factors in the capacity of short dsRNAs to activate OAS1. These helical features may facilitate more ready adoption of the distorted OAS1-bound conformation or stabilize important structures to predispose the dsRNA for optimal binding and activation of OAS1. These studies thus reveal the molecular basis for the greater capacity of some short dsRNAs to activate OAS1 in a sequence-independent manner.

摘要

2′-5′寡聚腺苷酸合成酶(OAS)是细胞浆双链 RNA(dsRNA)的先天免疫传感器,在限制病毒感染方面发挥着关键作用。这些蛋白质如何避免被细胞 RNA 异常激活还不完全清楚,但腺苷到次黄嘌呤(A-to-I)编辑已被提议用于限制可能导致 OAS/RNase L 途径刺激的内源性 RNA 的积累。在这里,我们旨在揭示这种序列修饰是否以及如何限制短的、定义明确的 dsRNA 激活单结构域 OAS1 的能力。出乎意料的是,我们发现所有测试的含次黄嘌呤的 dsRNA 都增加了激活 OAS1 的能力,无论是在不稳定的(I•U)还是标准 Watson-Crick 样碱基配对(I-C)环境中。具有强烈不稳定 A•C 错配或稳定 G-C 对的其他变体也表现出增加激活 OAS1 的能力,从而消除了螺旋稳定性作为 dsRNA 相对激活 OAS1 能力的因素。使用热差光谱和分子动力学模拟,我们确定了增加的螺旋动力学和螺旋结构的特定局部变化是短 dsRNA 激活 OAS1 的能力的重要因素。这些螺旋特征可能有助于更易于采用扭曲的 OAS1 结合构象,或者稳定重要的结构,使 dsRNA 能够最佳地结合和激活 OAS1。这些研究因此揭示了一些短 dsRNA 以序列非依赖性方式更有效地激活 OAS1 的分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7c6/8784149/4922ea00ffb7/pnas.2107111119fig01.jpg

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