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基孔肯雅病毒与热休克同源蛋白70相互作用以促进其进入蚊细胞系。

Chikungunya Virus Interacts with Heat Shock Cognate 70 Protein to Facilitate Its Entry into Mosquito Cell Line.

作者信息

Ghosh Ayushman, Desai Anita, Ravi Vasanthapuram, Narayanappa Gayathri, Tyagi Brij Kishore

机构信息

Department of Neurovirology, National Institute of Mental Health and Neurosciences, Bangalore, India.

Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.

出版信息

Intervirology. 2017;60(6):247-262. doi: 10.1159/000489308. Epub 2018 Jun 28.

Abstract

AIM

The study was designed to identify putative Chikungunya virus (CHIKV) receptor/s on C6/36 cells that facilitate viral entry.

METHODS

The virus overlay protein binding assay (VOPBA) was adopted to identify CHIKV-interacting bands present in C6/36 cell membrane and identity of the protein was established by mass spectrometry. The role of this protein as a putative CHIKV receptor on C6/36 cells was confirmed by infection inhibition assay. Cell surface localization of the identified protein was studied by indirect immunofluorescence assay (IFA) on nonpermeabilized cells and by flow cytometry. Interaction between this protein and CHIKV was confirmed by co-immunoprecipation (Co-IP) and Western blotting. The effect of depletion of the identified protein by quercetin was demonstrated by infection inhibition assay.

RESULTS

A 70-kDa protein was identified as a CHIKV-interacting protein by VOPBA. MALDI-TOF analysis followed by homology search revealed that this protein could be heat shock cognate 70 (HSC 70). Anti-HSC 70 antibodies blocked CHIKV entry into C6/36 cells in a dose-dependent manner. IFA and flow cytometry analysis demonstrated HSC 70 localization on C6/36 cell surface. Co-IP experiments confirmed the interaction between HSC 70 and CHIKV envelope. Quercetin- and YM-01-treated C6/36 cells exhibited dose-dependent infection inhibition.

CONCLUSION

HSC 70 serves as a putative CHIKV receptor on C6/36 cells.

摘要

目的

本研究旨在鉴定促进病毒进入的C6/36细胞上的假定基孔肯雅病毒(CHIKV)受体。

方法

采用病毒覆盖蛋白结合试验(VOPBA)鉴定C6/36细胞膜中存在的与CHIKV相互作用的条带,并通过质谱确定该蛋白的身份。通过感染抑制试验证实该蛋白作为C6/36细胞上假定CHIKV受体的作用。通过对未通透细胞的间接免疫荧光试验(IFA)和流式细胞术研究鉴定蛋白的细胞表面定位。通过共免疫沉淀(Co-IP)和蛋白质印迹法证实该蛋白与CHIKV之间的相互作用。通过感染抑制试验证明槲皮素对鉴定蛋白的消耗作用。

结果

通过VOPBA鉴定出一种70 kDa的蛋白为与CHIKV相互作用的蛋白。随后进行的基质辅助激光解吸电离飞行时间(MALDI-TOF)分析及同源性搜索表明该蛋白可能是热休克同源蛋白70(HSC 70)。抗HSC 70抗体以剂量依赖方式阻断CHIKV进入C6/36细胞。IFA和流式细胞术分析表明HSC 70定位于C6/36细胞表面。Co-IP实验证实HSC 70与CHIKV包膜之间存在相互作用。经槲皮素和YM-01处理的C6/36细胞表现出剂量依赖性的感染抑制。

结论

HSC 70作为C6/36细胞上的假定CHIKV受体。

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