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利用 SAMDI 质谱法无标记筛选 SARS-CoV-2 NSP14 外切酶活性

Label-Free Screening of SARS-CoV-2 NSP14 Exonuclease Activity Using SAMDI Mass Spectrometry.

机构信息

SAMDI Tech, Inc., Chicago, IL, USA.

Aligos Therapeutics, Inc., South San Francisco, CA, USA.

出版信息

SLAS Discov. 2021 Jul;26(6):766-774. doi: 10.1177/24725552211008854. Epub 2021 Apr 17.

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the virus responsible for the global COVID-19 pandemic. Nonstructural protein 14 (NSP14), which features exonuclease (ExoN) and guanine N7 methyltransferase activity, is a critical player in SARS-CoV-2 replication and fidelity and represents an attractive antiviral target. Initiating drug discovery efforts for nucleases such as NSP14 remains a challenge due to a lack of suitable high-throughput assay methodologies. This report describes the combination of self-assembled monolayers and matrix-assisted laser desorption ionization mass spectrometry to enable the first label-free and high-throughput assay for NSP14 ExoN activity. The assay was used to measure NSP14 activity and gain insight into substrate specificity and the reaction mechanism. Next, the assay was optimized for kinetically balanced conditions and miniaturized, while achieving a robust assay (Z factor > 0.8) and a significant assay window (signal-to-background ratio > 200). Screening 10,240 small molecules from a diverse library revealed candidate inhibitors, which were counterscreened for NSP14 selectivity and RNA intercalation. The assay methodology described here will enable, for the first time, a label-free and high-throughput assay for NSP14 ExoN activity to accelerate drug discovery efforts and, due to the assay flexibility, can be more broadly applicable for measuring other enzyme activities from other viruses or implicated in various pathologies.

摘要

严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)是引发全球 COVID-19 大流行的病毒。非结构蛋白 14(NSP14)具有核酸外切酶(ExoN)和鸟嘌呤 N7 甲基转移酶活性,是 SARS-CoV-2 复制和保真度的关键因素,也是有吸引力的抗病毒靶点。由于缺乏合适的高通量测定方法,启动针对 NSP14 等核酶的药物发现工作仍然具有挑战性。本报告介绍了自组装单层和基质辅助激光解吸电离质谱联用,首次实现了用于 NSP14 ExoN 活性的无标记和高通量测定。该测定法用于测量 NSP14 的活性,并深入了解其底物特异性和反应机制。接下来,对测定法进行了优化,以达到动力学平衡条件和微型化,同时实现了稳健的测定(Z 因子>0.8)和显著的测定窗口(信号与背景比>200)。从多样化文库中筛选 10240 种小分子化合物,发现了候选抑制剂,并对其进行了 NSP14 选择性和 RNA 嵌入的对抗筛选。此处描述的测定方法将首次实现用于 NSP14 ExoN 活性的无标记和高通量测定,从而加速药物发现工作,并且由于测定方法具有灵活性,因此可以更广泛地用于测量其他病毒或涉及各种病理的其他酶的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c42/8940776/657551366681/gr1.jpg

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