Epitope-focused immunogen design based on the ebolavirus glycoprotein HR2-MPER region

Abstract

The three human pathogenic ebolaviruses: Zaire (EBOV), Bundibugyo (BDBV), and Sudan (SUDV) virus, cause severe disease with high fatality rates. Epitopes of ebolavirus glycoprotein (GP) recognized by antibodies with binding breadth for all three ebolaviruses are of major interest for rational vaccine design. In particular, the heptad repeat 2 –membrane-proximal external region (HR2-MPER) epitope is relatively conserved between EBOV, BDBV, and SUDV GP and targeted by human broadly-neutralizing antibodies. To study whether this epitope can serve as an immunogen for the elicitation of broadly-reactive antibody responses, protein design in Rosetta was employed to transplant the HR2-MPER epitope identified from a co-crystal structure with the known broadly-reactive monoclonal antibody (mAb) BDBV223 onto smaller scaffold proteins. From computational analysis, selected immunogen designs were produced as recombinant proteins and functionally validated, leading to the identification of a sterile alpha motif (SAM) domain displaying the BDBV-HR2-MPER epitope near its C terminus as a promising candidate. The immunogen was fused to one component of a self-assembling, two-component nanoparticle and tested for immunogenicity in rabbits. Robust titers of cross-reactive serum antibodies to BDBV and EBOV GPs and moderate titers to SUDV GP were induced following immunization. To confirm the structural composition of the immunogens, solution NMR studies were conducted and revealed structural flexibility in the C-terminal residues of the epitope. Overall, our study represents the first report on an epitope-focused immunogen design based on the structurally challenging BDBV-HR2-MPER epitope.

Document Details

Document Type
Pub Defense Publication
Publication Date
May 18, 2022
Source ID
10.1371/journal.ppat.1010518

Entities

People

  • Alexander Bukreyev
  • Amandeep K. Sangha
  • Brooke Fiala
  • Clara T. Schoeder
  • Cristina E. Martina
  • Delphine C. Malherbe
  • Elad Binshtein
  • Erica Armstrong
  • James E. Crowe, Jr.
  • Jens Meiler
  • Jessica Rodriguez
  • Jinhui Dong
  • Kaitlyn V. Ledwitch
  • Lauren E Williamson
  • Natalia Kuzmina
  • Neil P. King
  • Pavlo Gilchuk
  • Rachel Nargi
  • Rachel Sutton
  • Xuan Zhang

Organizations

  • Defense Threat Reduction Agency
  • Gates Foundation
  • National Center for Research Resources
  • National Institute of Allergy and Infectious Diseases
  • National Science Foundation
  • Vanderbilt University

Tags

Fields of Study

  • Biology

Readers

  • Immunology
  • Infectious Disease/Epidemiology
  • Molecular and Cellular Biochemistry

Technology Areas

  • Biotechnology
  • Space