Visualisation and analysis of hepatitis C virus non-structural proteins using super-resolution microscopy

被引:5
|
作者
Bartlett, Christopher
Curd, Alistair
Peckham, Michelle [1 ]
Harris, Mark [1 ]
机构
[1] Univ Leeds, Fac Biol Sci, Sch Mol & Cellular Biol, Leeds LS2 9JT, W Yorkshire, England
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
英国惠康基金;
关键词
NS5A PROTEIN; MEMBRANOUS REPLICATION; QUANTITATIVE-ANALYSIS; DIFFRACTION-LIMIT; COMPLEX-FORMATION; CLUSTER-ANALYSIS; RNA-POLYMERASE; VIRAL GENOME; PALM; INHIBITORS;
D O I
10.1038/s41598-018-31861-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hepatitis C virus (HCV) RNA replication occurs in the cytosol of infected cells within a specialised membranous compartment. How the viral non-structural (NS) proteins are associated and organised within these structures remains poorly defined. We employed a super-resolution microscopy approach to visualise NS3 and NS5A in HCV infected cells. Using single molecule localisation microscopy, both NS proteins were resolved as clusters of localisations smaller than the diffraction-limited volume observed by wide-field. Analysis of the protein clusters identified a significant difference in size between the NS proteins. We also observed a reduction in NS5A cluster size following inhibition of RNA replication using daclatasvir, a phenotype which was maintained in the presence of the Y93H resistance associated substitution and not observed for NS3 clusters. These results provide insight into the NS protein organisation within hepatitis C virus RNA replication complexes and the mode of action of NS5A inhibitors.
引用
收藏
页数:12
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