Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1

Chikungunya virus (CHIKV) causes a debilitating arthralgic inflammatory disease in humans. The multifunctional CHIKV protein, nsP1, facilitates virus RNA replication and transcription by anchoring the viral replication complex (RC) to plasma membrane vesicles and synthesizing the viral RNA 5' c...

Full description

Saved in:
Bibliographic Details
Main Authors: Zhang, Kuo, Law, Yee-Song, Law, Michelle Cheok Yien, Tan, Yaw Bia, Wirawan, Melissa, Luo, Dahai
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2022
Subjects:
Online Access:https://hdl.handle.net/10356/157046
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-157046
record_format dspace
spelling sg-ntu-dr.10356-1570462023-02-28T17:11:58Z Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1 Zhang, Kuo Law, Yee-Song Law, Michelle Cheok Yien Tan, Yaw Bia Wirawan, Melissa Luo, Dahai School of Biological Sciences Lee Kong Chian School of Medicine (LKCMedicine) NTU Institute of Structural Biology Science::Biological sciences Chikungunya Virus RNA Cap Chikungunya virus (CHIKV) causes a debilitating arthralgic inflammatory disease in humans. The multifunctional CHIKV protein, nsP1, facilitates virus RNA replication and transcription by anchoring the viral replication complex (RC) to plasma membrane vesicles and synthesizing the viral RNA 5' cap-0. Here, we report a cryo-EM structure of CHIKV nsP1 at 2.38 Å resolution. Twelve copies of nsP1 form a crown-shaped ring structure with a 7.5-nm-wide channel for mediating communication and exchange between the viral RC and the host cell. The catalytic site for viral RNA capping is located in a tunnel that is shaped by neighboring nsP1 molecules. Two membrane-association loops target nsP1 to the inner leaflet of the plasma membrane via palmitoylation and hydrophobic and electrostatic interactions. Our study provides the structural basis of viral RNA capping and RC assembly mediated by nsP1 and guides the development of antivirals targeting these essential steps of virus infection. Ministry of Education (MOE) Ministry of Health (MOH) National Medical Research Council (NMRC) Submitted/Accepted version This research is supported by the Republic of Singapore Ministry of Education under its Ministry of Education Academic Research Fund Tier 2 (MOE2016-T2- 2-097) and Education Academic Research Fund Tier 1 (2018-T1-002-010) and by the Republic of Singapore Ministry of Health’s National Medical Research Council under its Open Fund – individual Research Grant (OF-IRG) (NMRC/ OFIRG/0075/2018.). 2022-05-01T05:16:25Z 2022-05-01T05:16:25Z 2021 Journal Article Zhang, K., Law, Y., Law, M. C. Y., Tan, Y. B., Wirawan, M. & Luo, D. (2021). Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1. Cell Host & Microbe, 29(5), 757-764. https://dx.doi.org/10.1016/j.chom.2021.02.018 1931-3128 https://hdl.handle.net/10356/157046 10.1016/j.chom.2021.02.018 33730549 2-s2.0-85105434618 5 29 757 764 en MOE2016-T2- 2-097 2018-T1-002-010 NMRC/ OFIRG/0075/2018 Cell Host & Microbe © 2021 Elsevier Inc. All rights reserved. This paper was published in Cell Host & Microbe and is made available with permission of Elsevier Inc. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences
Chikungunya Virus
RNA Cap
spellingShingle Science::Biological sciences
Chikungunya Virus
RNA Cap
Zhang, Kuo
Law, Yee-Song
Law, Michelle Cheok Yien
Tan, Yaw Bia
Wirawan, Melissa
Luo, Dahai
Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1
description Chikungunya virus (CHIKV) causes a debilitating arthralgic inflammatory disease in humans. The multifunctional CHIKV protein, nsP1, facilitates virus RNA replication and transcription by anchoring the viral replication complex (RC) to plasma membrane vesicles and synthesizing the viral RNA 5' cap-0. Here, we report a cryo-EM structure of CHIKV nsP1 at 2.38 Å resolution. Twelve copies of nsP1 form a crown-shaped ring structure with a 7.5-nm-wide channel for mediating communication and exchange between the viral RC and the host cell. The catalytic site for viral RNA capping is located in a tunnel that is shaped by neighboring nsP1 molecules. Two membrane-association loops target nsP1 to the inner leaflet of the plasma membrane via palmitoylation and hydrophobic and electrostatic interactions. Our study provides the structural basis of viral RNA capping and RC assembly mediated by nsP1 and guides the development of antivirals targeting these essential steps of virus infection.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Zhang, Kuo
Law, Yee-Song
Law, Michelle Cheok Yien
Tan, Yaw Bia
Wirawan, Melissa
Luo, Dahai
format Article
author Zhang, Kuo
Law, Yee-Song
Law, Michelle Cheok Yien
Tan, Yaw Bia
Wirawan, Melissa
Luo, Dahai
author_sort Zhang, Kuo
title Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1
title_short Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1
title_full Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1
title_fullStr Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1
title_full_unstemmed Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1
title_sort structural insights into viral rna capping and plasma membrane targeting by chikungunya virus nonstructural protein 1
publishDate 2022
url https://hdl.handle.net/10356/157046
_version_ 1759857591951818752