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TMPyP4、BRACO19和PhenDC3对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)基因组G-四链体结构的稳定作用

Stabilization of G-Quadruplex Structures of the SARS-CoV-2 Genome by TMPyP4, BRACO19, and PhenDC3.

作者信息

Cervenak Miklós, Molnár Orsolya Réka, Horváth Péter, Smeller László

机构信息

Department of Biophysics and Radiation Biology, Semmelweis University, 1094 Budapest, Hungary.

Department of Pharmaceutical Chemistry, Semmelweis University, 1092 Budapest, Hungary.

出版信息

Int J Mol Sci. 2024 Feb 20;25(5):2482. doi: 10.3390/ijms25052482.

Abstract

The G-quadruplex is one of the non-canonical structures formed by nucleic acids, which can be formed by guanine-rich sequences. They became the focus of much research when they were found in several oncogene promoter regions and also in the telomeres. Later on, they were discovered in viruses as well. Various ligands have been developed in order to stabilize DNA G-quadruplexes, which were believed to have an anti-cancer or antiviral effect. We investigated three of these ligands, and whether they can also affect the stability of the G-quadruplex-forming sequences of the RNA genome of SARS-CoV-2. All three investigated oligonucleotides showed the G-quadruplex form. We characterized their stability and measured their thermodynamic parameters using the Förster resonance energy transfer method. The addition of the ligands caused an increase in the unfolding temperature, but this effect was smaller compared to that found earlier in the case of G-quadruplexes of the hepatitis B virus, which has a DNA genome.

摘要

G-四链体是由核酸形成的非经典结构之一,可由富含鸟嘌呤的序列形成。当它们在几个癌基因启动子区域以及端粒中被发现时,成为了众多研究的焦点。后来,它们也在病毒中被发现。为了稳定DNA G-四链体,人们开发了各种配体,据信这些配体具有抗癌或抗病毒作用。我们研究了其中三种配体,以及它们是否也能影响严重急性呼吸综合征冠状病毒2(SARS-CoV-2)RNA基因组中形成G-四链体的序列的稳定性。所有三种被研究的寡核苷酸都呈现出G-四链体形式。我们对它们的稳定性进行了表征,并使用Förster共振能量转移方法测量了它们的热力学参数。配体的添加导致解链温度升高,但与之前在具有DNA基因组的乙型肝炎病毒的G-四链体中发现的效应相比,这种效应较小。

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