1. Academic Validation
  2. The interaction of GRP78 and Zika virus E and NS1 proteins occurs in a chaperone-client manner

The interaction of GRP78 and Zika virus E and NS1 proteins occurs in a chaperone-client manner

  • Sci Rep. 2024 May 6;14(1):10407. doi: 10.1038/s41598-024-61195-z.
Wannapa Sornjai 1 Ploenphit Promma 1 Suphansa Priewkhiew 1 Suwipa Ramphan 1 Janejira Jaratsittisin 1 Pailin Jinagool 1 Nitwara Wikan 1 2 Michael Greenwood 3 David Murphy 3 Duncan R Smith 4
Affiliations

Affiliations

  • 1 Molecular Pathology Laboratory, Institute of Molecular Biosciences, Mahidol University, 25/25 Phutthamonthon Sai 4 Road, Salaya, Nakhon Pathom, 73170, Thailand.
  • 2 Department of Pharmacology, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200, Thailand.
  • 3 Molecular Neuroendocrinology Research Group, Bristol Medical School, Translational Health Sciences, University of Bristol, Bristol, UK.
  • 4 Molecular Pathology Laboratory, Institute of Molecular Biosciences, Mahidol University, 25/25 Phutthamonthon Sai 4 Road, Salaya, Nakhon Pathom, 73170, Thailand. duncan_r_smith@hotmail.com.
Abstract

Glucose regulated protein 78 (GRP78) is a chaperone protein that is a central mediator of the unfolded protein response, a key cellular stress response pathway. GRP78 has been shown to be critically required for Infection and replication of a number of flaviviruses, and to interact with both non-structural (NS) and structural Flavivirus proteins. However, the nature of the specific interaction between GRP78 and Viral Proteins remains largely unknown. This study aimed to characterize the binding domain and critical amino acid residues that mediate the interaction of GRP78 to ZIKV E and NS1 proteins. Recombinant EGFP fused GRP78 and individual subdomains (the nucleotide binding domain (NBD) and the substrate binding domain (SBD)) were used as a bait protein and co-expressed with full length or truncated ZIKV E and NS1 proteins in HEK293T/17 cells. Protein-protein interactions were determined by a co-immunoprecipitation assay. From the results, both the NBD and the SBD of GRP78 were crucial for an effective interaction. Single amino acid substitutions in the SBD showed that R492E and T518A mutants significantly reduced the binding affinity of GRP78 to ZIKV E and NS1 proteins. Notably, the interaction of GRP78 with ZIKV E was stably maintained against various single amino acid substitutions on ZIKV E domain III and with all truncated ZIKV E and NS1 proteins. Collectively, the results suggest that the principal binding between GRP78 and Viral Proteins is mainly a classic canonical chaperone protein-client interaction. The blocking of GRP78 chaperone function effectively inhibited ZIKV Infection and replication in neuronal progenitor cells. Our findings reveal that GRP78 is a potential host target for anti-ZIKV therapeutics.

Keywords

Chaperone; Critical residues; GRP78; GRP78 inhibitor; ZIKV E; ZIKV NS1; Zika virus.

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