Abstract
Influenza virus is thought to assemble in raft domains of the plasma membrane, but many of the conclusions were based on (controversial) Triton extraction experiments. Here we review how sophisticated methods of fluorescence microscopy, such as FPALM, FRET and FRAP, contributed to our understanding of lipid domain association of the viral proteins HA and M2. The results are summarized in light of the current model for virus assembly and lipid domain organization. Finally, it is described how the signals that govern domain association in transfected cells affect replication of influenza virus.
© 2012 Blackwell Publishing Ltd.
Publication types
-
Research Support, Non-U.S. Gov't
-
Review
MeSH terms
-
Animals
-
CHO Cells
-
Cricetinae
-
Fluorescence Recovery After Photobleaching
-
Fluorescence Resonance Energy Transfer
-
Hemagglutinin Glycoproteins, Influenza Virus / chemistry
-
Hemagglutinin Glycoproteins, Influenza Virus / metabolism*
-
Humans
-
Membrane Microdomains / chemistry*
-
Membrane Microdomains / metabolism
-
Membrane Microdomains / virology
-
Microscopy, Fluorescence
-
Orthomyxoviridae / chemistry*
-
Orthomyxoviridae / physiology
-
Transfection
-
Viral Matrix Proteins / chemistry
-
Viral Matrix Proteins / metabolism*
-
Virus Assembly
-
Virus Replication
Substances
-
Hemagglutinin Glycoproteins, Influenza Virus
-
M2 protein, Influenza A virus
-
Viral Matrix Proteins