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SARS-CoV-2基因组中生理温度下稳定RNA G-三链体结构的实验与计算证据

Experimental and Computational Evidence of a Stable RNA G-Triplex Structure at Physiological Temperature in the SARS-CoV-2 Genome.

作者信息

Campanile Marco, Improta Roberto, Esposito Luciana, Platella Chiara, Oliva Rosario, Del Vecchio Pompea, Winter Roland, Petraccone Luigi

机构信息

Department of Chemical Sciences, University of Naples Federico II, Via Cintia 4, 80126, Naples, Italy.

Institute of Biostructure and Bioimaging, National Research Council CNR, Via P. Castellino 111, 80131, Naples, Italy.

出版信息

Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202415448. doi: 10.1002/anie.202415448. Epub 2024 Nov 6.

Abstract

RG1 is a quadruplex-forming sequence in the SARS-CoV-2 genome proposed as possible therapeutic target for COVID-19. We demonstrate that the dominant conformation of RG1 under physiological conditions differs from the parallel quadruplex previously assumed. Through comprehensive investigations employing CD, UV, NMR, DSC, gel electrophoresis, MD simulations, in silico spectroscopy and the use of truncated RG1 sequences, we have identified this stable conformation as an RNA G-triplex composed of two G-triads. We believe this previously unreported RNA structure could serve as a novel therapeutic target. Our findings open new avenues for further studies on the presence and biological role of RNA G-triplexes in vivo.

摘要

RG1是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)基因组中一种能形成四链体的序列,被提议作为治疗新冠肺炎(COVID-19)的潜在靶点。我们证明,RG1在生理条件下的主要构象与之前假定的平行四链体不同。通过运用圆二色光谱(CD)、紫外光谱(UV)、核磁共振(NMR)、差示扫描量热法(DSC)、凝胶电泳、分子动力学(MD)模拟、计算机模拟光谱以及使用截短的RG1序列进行全面研究,我们确定这种稳定构象是一种由两个G-三联体组成的RNA G-三链体。我们认为这种此前未报道的RNA结构可能成为一种新的治疗靶点。我们的研究结果为进一步研究RNA G-三链体在体内的存在情况及其生物学作用开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2a/11656141/547cef55fd4c/ANIE-63-e202415448-g005.jpg

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