SLiM-binding pockets: an attractive target for broad-spectrum antivirals

被引:8
|
作者
Simonetti, Leandro [1 ]
Nilsson, Jakob [2 ]
McInerney, Gerald [3 ]
Ivarsson, Ylva [1 ]
Davey, Norman E. [4 ]
机构
[1] Dept Chem BMC, Husargatan 3, S-75123 Uppsala, Sweden
[2] Univ Copenhagen, Novo Nord Fdn Ctr Prot Res, Fac Hlth & Med Sci, Blegdamsvej 3B, DK-2200 Copenhagen, Denmark
[3] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Stockholm, Sweden
[4] Inst Canc Res, Div Canc Biol, 237 Fulham Rd, London SW3 6JB, England
关键词
PROTEIN; EBOLA; IDENTIFICATION; INNOVATION; LEUKEMIA; MOTIFS; DOMAIN;
D O I
10.1016/j.tibs.2022.12.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Short linear motif (SLiM)-mediated interactions offer a unique strategy for viral intervention due to their compact interfaces, ease of convergent evolution, and key functional roles. Consequently, many viruses extensively mimic host SLiMs to hijack or deregulate cellular pathways and the same motif-binding pocket is often targeted by numerous unrelated viruses. A toolkit of therapeutics targeting commonly mimicked SLiMs could provide prophylactic and therapeutic broadspectrum antivirals and vastly improve our ability to treat ongoing and future viral outbreaks. In this opinion article, we discuss the therapeutic relevance of SLiMs, advocating their suitability as targets for broad-spectrum antiviral inhibitors.
引用
收藏
页码:420 / 427
页数:8
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