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SARS-CoV-2 刺突蛋白与淀粉样蛋白的相互作用:神经退行性变的潜在线索。

SARS-CoV-2 spike protein interactions with amyloidogenic proteins: Potential clues to neurodegeneration.

机构信息

Faculty of Allied Health Sciences, Shree Guru Gobind Singh Tricentenary University, Gurugram, Haryana, 122505, India.

Amity Institute of Neuropsychology & Neurosciences, Amity University, Noida, UP, 201303, India.

出版信息

Biochem Biophys Res Commun. 2021 May 21;554:94-98. doi: 10.1016/j.bbrc.2021.03.100. Epub 2021 Mar 24.

Abstract

The post-infection of COVID-19 includes a myriad of neurologic symptoms including neurodegeneration. Protein aggregation in brain can be considered as one of the important reasons behind the neurodegeneration. SARS-CoV-2 Spike S1 protein receptor binding domain (SARS-CoV-2 S1 RBD) binds to heparin and heparin binding proteins. Moreover, heparin binding accelerates the aggregation of the pathological amyloid proteins present in the brain. In this paper, we have shown that the SARS-CoV-2 S1 RBD binds to a number of aggregation-prone, heparin binding proteins including Aβ, α-synuclein, tau, prion, and TDP-43 RRM. These interactions suggests that the heparin-binding site on the S1 protein might assist the binding of amyloid proteins to the viral surface and thus could initiate aggregation of these proteins and finally leads to neurodegeneration in brain. The results will help us to prevent future outcomes of neurodegeneration by targeting this binding and aggregation process.

摘要

新冠病毒感染后包括一系列神经症状,包括神经退行性变。脑内蛋白聚集被认为是神经退行性变背后的重要原因之一。SARS-CoV-2 刺突 S1 蛋白受体结合域(SARS-CoV-2 S1 RBD)与肝素和肝素结合蛋白结合。此外,肝素结合加速了脑内存在的病理淀粉样蛋白的聚集。在本文中,我们表明 SARS-CoV-2 S1 RBD 与许多易于聚集的肝素结合蛋白结合,包括 Aβ、α-突触核蛋白、tau、朊病毒和 TDP-43 RRM。这些相互作用表明 S1 蛋白上的肝素结合位点可能有助于淀粉样蛋白与病毒表面的结合,从而可能引发这些蛋白的聚集,并最终导致脑内神经退行性变。这些结果将有助于我们通过靶向这种结合和聚集过程来预防未来的神经退行性变结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02fe/7988450/2193320dba75/gr1_lrg.jpg

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