Influenza Hemagglutinin Structures and Antibody Recognition
- 1Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California 92037, USA
- 2The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, California 92037, USA
- Correspondence: wilson{at}scripps.edu
Abstract
Hemagglutinin (HA) is most abundant glycoprotein on the influenza virus surface. Influenza HA promotes viral entry by engaging the receptor and mediating virus–host membrane fusion. At the same time, HA is the major antigen of the influenza virus. HA antigenic shift can result in pandemics, whereas antigenic drift allows human circulating strains to escape herd immunity. Most antibody responses against HA are strain-specific. However, antibodies that have neutralizing activities against multiple strains or even subtypes have now been discovered and characterized. These broadly neutralizing antibodies (bnAbs) target conserved regions on HA, such as the receptor-binding site and the stem domain. Structural studies of such bnAbs have provided important insight into universal influenza vaccine and therapeutic design. This review discusses the HA functions as well as HA–antibody interactions from a structural perspective.
