Molecular Basis for Antiviral Action of EDP‐235: A Potent and Selective SARS‐CoV‐2 3CLpro Inhibitor for the Treatment of Covid 19

IC50型 蛋白酶 化学 活动站点 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 冠状病毒 2019年冠状病毒病(COVID-19) 体外 生物化学 离解常数 药理学 分子生物学 生物 受体 医学 传染病(医学专业) 疾病 内科学
作者
Anand Balakrishnan,Archie Reyes,Ruichao Shen,Nalini Bisht,Joyce Sweeney,Rachel Levene,Nicole McAllister,Tessa Cressey,Nathan Manalo,Michael H. J. Rhodin,Michael Vaine,Guoqiang Wang,Yat Sun Or,Bryan Goodwin
出处
期刊:The FASEB Journal [Wiley]
卷期号:36 (S1) 被引量:8
标识
DOI:10.1096/fasebj.2022.36.s1.0r514
摘要

To date, there are no approved oral antiviral therapies that can be administered early in the course of COVID-19 to suppress progression of the disease or for prophylaxis. EDP-235 is a potent and selective inhibitor of SARS-CoV-2 3C-like protease (3CLpro). EDP-235 inhibits SARS-CoV-2 3CLpro protease activity with an IC50 of 5.8 ± 3.7 nM and retains its activity against variant 3CLpro proteins from multiple SARS-CoV-2 lineages (IC50 range of 2.8--5.8 nM). 3CLpro protease activity progress curves showed significant curvature in a time- and EDP-235-concentration-dependent manner indicative of slow-onset inhibition. Slow reversal of inhibition of SARS-CoV-2 3CLpro enzyme activity was observed in a jump dilution experiment. Michaelis-Menten kinetic studies with a FRET peptide substrate in the presence of EDP-235 indicated that EDP-235 is a substrate-competitive inhibitor of SARS-CoV-2 3CLpro with an overall dissociation constant Ki of 3.0 ± 1.6 nM. SARS-CoV-2 3CLpro was crystallized bound to a close analog of EDP-235 and structure elucidation revealed that the ligand bound at the active site and interacted with side chains of conserved residues Cys-145, His-163, and Glu-166. EDP-235 also potently inhibits 3CLpro enzymes from other α-coronaviruses (IC50 range of 2-4 nM) and β-coronaviruses (SARS-CoV IC50 of 5.4 nM, MERS-CoV IC50 of 70 nM) which cause disease in humans to date. EDP-235 resistance mutations in HCoV-229E map to the active site of 3CLpro close to the predicted binding site and offer additional support to the mechanism of inhibition. EDP-235 also showed a favorable selectivity profile (>300 selectivity index) when tested against a panel of 30 mammalian proteases. In summary, EDP-235 acts as a slow-onset, slow-reversible, substrate-competitive inhibitor of SARS-CoV-2 3CLpro. The outstanding preclinical profile of EDP-235 supports its further evaluation as an oral therapeutic for the management of COVID-19.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Postgraduate-Z完成签到,获得积分10
1秒前
bmt关闭了bmt文献求助
2秒前
所所应助wang采纳,获得10
2秒前
2秒前
asdfghjkl发布了新的文献求助10
3秒前
3秒前
刻苦的晓蕾完成签到,获得积分10
3秒前
zhl完成签到,获得积分10
3秒前
愛迪完成签到,获得积分10
4秒前
gy关闭了gy文献求助
4秒前
脆脆Shark完成签到,获得积分10
6秒前
坚强白凝完成签到,获得积分10
9秒前
10秒前
zho发布了新的文献求助10
10秒前
chizhi完成签到,获得积分10
12秒前
13秒前
希望天下0贩的0应助花花采纳,获得10
13秒前
q792309106发布了新的文献求助10
14秒前
小马甲应助杜兰特采纳,获得10
16秒前
CipherSage应助zxcv采纳,获得10
16秒前
17秒前
天天快乐应助安生生采纳,获得10
18秒前
小马宝莉完成签到,获得积分10
21秒前
思源应助曹松柏采纳,获得10
21秒前
22秒前
田様应助a123采纳,获得10
23秒前
小新发布了新的文献求助20
24秒前
24秒前
核桃发布了新的文献求助10
26秒前
26秒前
27秒前
27秒前
阔达冰兰发布了新的文献求助10
28秒前
28秒前
29秒前
中和皇极应助曹沛岚采纳,获得10
30秒前
安生生发布了新的文献求助10
30秒前
花花发布了新的文献求助10
31秒前
杜兰特发布了新的文献求助10
32秒前
33秒前
高分求助中
The Mother of All Tableaux: Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 3000
Social Research Methods (4th Edition) by Maggie Walter (2019) 1030
A new approach to the extrapolation of accelerated life test data 1000
Indomethacinのヒトにおける経皮吸収 400
基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 370
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
Robot-supported joining of reinforcement textiles with one-sided sewing heads 320
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3993503
求助须知:如何正确求助?哪些是违规求助? 3534194
关于积分的说明 11264895
捐赠科研通 3274061
什么是DOI,文献DOI怎么找? 1806259
邀请新用户注册赠送积分活动 883055
科研通“疑难数据库(出版商)”最低求助积分说明 809702