Activity-Based Phosphatidylinositol Kinase Probes Detect Changes to Protein-Protein Interactions During Hepatitis C Virus Replication

被引:9
|
作者
Desrochers, Genevieve F. [1 ]
Cornacchia, Christina [1 ]
McKay, Craig S. [1 ]
Pezacki, John Paul [1 ,2 ]
机构
[1] Univ Ottawa, Dept Chem & Biomol Sci, 10 Marie Curie Pvt, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Dept Biochem Microbiol & Immunol, 451 Smyth Rd, Ottawa, ON K1H 8M5, Canada
来源
ACS INFECTIOUS DISEASES | 2018年 / 4卷 / 05期
基金
加拿大自然科学与工程研究理事会;
关键词
activity-based protein profiling; protein-protein interactions; kinase; phosphatidylinositol; HISTONE DEACETYLASE COMPLEXES; CELL REGULATION; SMALL-MOLECULE; 3A PROTEIN; IN-VITRO; III-BETA; ACBD3; PHOSPHOINOSITIDES; TARGET; PI4KB;
D O I
10.1021/acsinfecdis.8b00047
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Protein-protein interactions are integral to host-virus interactions and can contribute significantly to enzyme regulation by changing the localization of both host and viral enzymes within the cell, inducing conformational change relevant to enzyme activity or recruiting other additional proteins to form functional complexes. Identifying the interactors of active enzymes using an activity-based protein profiling probe has allowed us to characterize both normal enzyme activation mechanisms and the manner by which these mechanisms are hijacked and altered by the hepatitis C virus (HCV). Here, we report use of a novel activity-based probe, PIKBPyne, which labels phosphatidylinositol kinases (PIKs) in an activity-based manner, to investigate HCV-dependent changes in protein-protein interactions for PI4KB. Herein, we report the synthesis of new variations on PIKBPyne, compare their ability to label the interacting partners of PI4KB, and demonstrate the utility of our approach in characterizing virus-mediated changes to host function.
引用
收藏
页码:752 / 757
页数:11
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