Broad-based spike protein stalk-based vaccine platform for SARS-CoV-2 and other coronaviruses

NIH RePORTER · NIH · R21 · $235,500 · view on reporter.nih.gov ↗

Abstract

Project Summary/Abstract We propose to develop a subunit vaccine for SARS-CoV-2, using a structure-based approach targeting conserved and functionally essential domains in the stalk region of the viral spike protein. We expect our vaccine platform to be applicable and effective across a wide range of existing and emerging coronaviruses. As our system is based on expression in E. coli is it expected to be cost–effective, and our stalk-based approach is specifically designed to cover a range of distinct coronaviruses. However, it is important to note that our vaccine platform is highly flexible, with the antigen able to be re-engineered rapidly in the face of a novel coronavirus that may emerge, and for which the vaccine developed in this application is not effective.

Key facts

NIH application ID
10493412
Project number
5R21AI166840-02
Recipient
CORNELL UNIVERSITY
Principal Investigator
Gary R Whittaker
Activity code
R21
Funding institute
NIH
Fiscal year
2022
Award amount
$235,500
Award type
5
Project period
2021-09-22 → 2024-08-31