Abstract
Cell entry of many enveloped viruses occurs by engagement with cellular receptors, followed by internalization into endocytic compartments and pH-induced membrane fusion. A previously unnoticed step of receptor switching was found to be critical during cell entry of two devastating human pathogens: Ebola and Lassa viruses. Our recent studies revealed the functional role of receptor switching to LAMP1 for triggering membrane fusion by Lassa virus and showed the involvement of conserved histidines in this switching, suggesting that other viruses from this family may also switch to LAMP1. However, when we investigated viruses that are genetically close to Lassa virus, we discovered that they cannot bind LAMP1. A crystal structure of the receptor-binding module from Morogoro virus revealed structural differences that allowed mapping of the LAMP1 binding site to a unique set of Lassa residues not shared by other viruses in its family, illustrating a key difference in the cell-entry mechanism of Lassa virus that may contribute to its pathogenicity.
MeSH terms
-
Amino Acid Sequence
-
Animals
-
Arenaviridae Infections / virology*
-
Arenaviruses, Old World / chemistry
-
Arenaviruses, Old World / genetics
-
Arenaviruses, Old World / metabolism*
-
Binding Sites
-
Humans
-
Lassa Fever / virology*
-
Lassa virus / chemistry
-
Lassa virus / genetics
-
Lassa virus / metabolism*
-
Lysosomal Membrane Proteins / chemistry*
-
Lysosomal Membrane Proteins / genetics
-
Lysosomal Membrane Proteins / metabolism
-
Membrane Fusion
-
Models, Molecular
-
Models, Structural
-
Protein Binding
-
Receptors, Cell Surface / chemistry
-
Receptors, Cell Surface / genetics
-
Receptors, Cell Surface / metabolism
-
Sequence Alignment
-
Species Specificity
Substances
-
LAMP1 protein, human
-
Lysosomal Membrane Proteins
-
Receptors, Cell Surface
Grants and funding
This research was supported by a research grant from the Enoch Foundation (RD), a research grant from the Abramson Family Center for Young Scientists (RD), a research grant from Ms. Rudolfine Steindling (RD), a grant from the Mizutani Foundation for Glycoscience (
http://www.mizutanifdn.or.jp/) (RD), and by the I-CORE Program of the Planning and Budgeting Committee and The Israel Science Foundation (
https://www.isf.org.il/#/) (grant No. 1775/12) (RD). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.