Virus Structure• Virus capsids function in: – Packaging and protecting nucleic acid – Host cell recognition • Protein on coat or envelope “feels” or “recognizes” host cell receptors – G
Trang 1Introduction to Virus Structure
Tutorial
Jonathan King, Peter Weigele, Greg Pintilie, David Gossard
(MIT) v.November, 2008
Trang 2• Protective Shell - Capsid
– Made of many identical protein
Trang 3Virus Structure
• Virus capsids function in:
– Packaging and protecting nucleic acid
– Host cell recognition
• Protein on coat or envelope “feels” or “recognizes” host cell receptors
– Genomic material delivery
• Enveloped: cell fusion event
• Non-enveloped: more complex strategies &
specialized structures
Trang 4Electron Microscopy
Mitra, K & Frank, J., 2006 Ribosome dynamics: insights from atomic structure modeling into cryo-electron
microscopy maps Annual review of biophysics and biomolecular structure, 35, 299-317.
Trang 5• In 1953, Crick & Watson proposed …
principles of virus structure
– Key insight:
• Limited volume of virion capsid => nucleic acid sufficient to code for only a few sorts of proteins of limited size
– Conclusion:
• Identical subunits in identical environments
• Icosahedral, dodecahedral symmetry
Trang 6X-ray Crystallography of Viruses
• Symmetry of protein shells makes them uniquely well-suited to crystallographic methods
• Viruses are the largest assemblies of biological macromolecules whose structures have been
determined at high resolution
Trang 8Similarity to Buckminster Fuller’s
Geodesic Domes
Trang 10Caspar and Klug’s Icosahedral
shell
Trang 11But …
• Clear evolutionary pressure to make larger capsid
– Using larger subunits helps very little
– Using more subunits helps a lot
• Not possible to form icosahedral shell (of identical units in identical environments) with more than 60 subunits
• Viruses with more than 60 subunits were observed
• Question :
– How can >60 subunits form an icosahedral shell?
– Will any number of subunits work?
– If so, how would they be organized?
Trang 12• In 1962, Caspar & Klug proposed the
theory of “quasi-equivalence”
– Not all protein subunits are equivalent
• “Identical” subunits in slightly different environments
– Only certain numbers of subunits will can be packed into closed regular lattice.
Caspar & Klug, Cold Spring Harbor, 1962
Trang 13– Shift from T1 to T4 packing
=> 8-fold increase in volume
Trang 14Spherical viruses have icosahedral symmetry
Trang 15Homunculattice
Trang 16HK97 Asymmetric Unit
Trang 17Herpes Simplex Virus at 8.5 Å resolution
Trang 18• Infection depends on spike proteins projecting from capsid membrane called “Hemagglutinin (HA)”
• These bind sugar molecules on cell surface
• Much of the difference between Hong Kong flu, Swine flu, Bird flu, and other strains, is in the amino acid sequence and conformation of the HA protein
• These differences control what host cell types the virus can infect
• Immunization against flu involves your immune system synthesizing antibody proteins that bind the HA protein
Trang 19Influenza virus
entry of influenzainto cell
composition of virus
Trang 20a pH induced, conformationally controlled trigger
for membrane fusion
backbone is structured
disordered loop
Qiao et al Membrane Fusion Activity of Influenza Hemagglutinin The Journal of Cell Biology, Volume 141, 1998
Trang 21Influenza Hemagglutinin
• The HA spikes extend like a spring during infection
Trang 22Trimer Structure
• Long alpha helices form
coiled coil structure
• In mature trimers of HA0,
each monomer is cleaved
into HA1 and HA2
Trang 23Evolution of dsDNA viruses
• All known viruses, whether infecting
bacteria or humans, may have evolved from
a single common ancestor, relatively early
in the evolution of organisms.
Trang 24Common steps in the assembly of all dsDNA
viruses
• Unique portal ring at one Vertex
• Scaffolding proteins
• Procapsid assembled empty of DNA
• DNA pumped into procapsid through portal ring
• DNA moves back through portal to enter
cell
Trang 26P22 Pathway
Trang 28Herpes viruses also have a portal protein
Herpes portal (UL6) tagged with gold-bead labeled antibodiesvisualized by negative stain electron microscopy
portalcomplex
Bill Newcomb and Jay Brown, University of Virginia
Trang 29Trus BL, Cheng N, Newcomb WW, Homa FL, Brown JC, Steven AC
Structure and polymorphism of the UL6 portal protein of herpes
Cryo-EM structure of purified Herpes portal protein