The Journal of Physical Chemistry BBiophysicsPeer-reviewed journal article
Coupled Binding and Folding of NS2B/NS3 Protease and Linker Effects Revealed by Topology-based Modeling
Kairong DongiD, Jian Wen HuangiD, Min CheniD, Jianhan CheniD
Abstract
Orthoflavivirus, such as West Nile Virus (WNV), dengue virus (DENV) and ZIKA virus (ZIKV), are globally distributed pathogens that pose substantial threats to human health. Currently, there are still no effective antiviral drugs for WNV or ZIKV. Despite the availability of two licensed DENV vaccines, their use remains limited due to potential risks, highlighting an urgent need for antiviral drug development. The highly conserved orthoflavivirus protease NS2B/NS3 is required for viral replication, making it a promising anti-flavivirus target. A major challenge, however, is the highly charged active site of this enzyme, which requires charged chemical matters with low bioavailability. An alternative and more attractive strategy is to target potential allosteric sites or folding intermediate states of the protease. In this work, we employ the topology-based coarse-grained G[o] modeling to explore the coupled binding and folding pathways of WNV NS2B/NS3 protease and study the effects of the widely used experimental construct with a G4SG4 linker between NS2B and NS3 on stability and folding. Our results provide a holistic conformational landscape of the protease binding and folding, including several key intermediate states. We find that the presence of the G4SG4 linker alters the folding pathways and destabilizes the NS2B C-terminus. The latter is consistent with experimental observations that the G4SG4 linked protease has lower activity and adopts an open state without the substrate in crystal structures. Together, these findings provide for the first time a complete picture of the binding and folding of the NS2B/NS3 protease and identify important folding intermediate states that could be targeted for allosteric antiviral drug development. TOC Figure O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=157 SRC="FIGDIR/small/722635v1_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@163c356org.highwire.dtl.DTLVardef@ad7b35org.highwire.dtl.DTLVardef@173ed8aorg.highwire.dtl.DTLVardef@1f026bf_HPS_FORMAT_FIGEXP M_FIG C_FIG
- assay: protein structure
- research focus: protein folding & dynamics
- research focus: drug response / drug discovery
- approach: deep learning
- approach: statistical model
- Citations
- 1
- FWCI
- 2.08
- Field percentile
- top 11%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Crystal structures of full length DENV4 NS2B-NS3 reveal the dynamic interaction between NS2B and NS3 upon binding to protease inhibitors
W. W. Phoo, A. El Sahili, … M. W. Chen·bioRxiv·Jan 27, 2020
- Allosteric inhibitors of Zika virus NS2B-NS3 protease targeting protease in super-open conformation
I. Meewan, S. Shiryaev, … R. Abagyan·bioRxiv·Mar 9, 2022
- Investigating the folding dynamics of NS2B protein of Zika virus
- Experimental and computational studies on molecular mechanism by which Curcumin allosterically inhibits Dengue protease
J. Song·bioRxiv·Sep 20, 2020
- Tuning single-molecule ClyA nanopore tweezers for real-time tracking ofthe conformational dynamics of West Nile viral NS2B/NS3 protease
Spencer A. Shorkey, Yumeng Zhang, … Min Chen·Biophysical JournalPeer-reviewed·Nov 22, 2024
- DUAL FUNCTION OF ZIKA VIRUS NS2B-NS3 PROTEASE
S. Shiryaev, P. Cieplak, … A. Terskikh·PLOS PathogensPeer-reviewed·Nov 27, 2023