Structural Insights into Adeno-Associated Virus Serotype 5
| Autor: | Nicholas Muzyczka, John A. Chiorini, Mavis Agbandje-McKenna, Michael A. DiMattia, Lakshmanan Govindasamy, Sergei Zolotukhin, Robert McKenna, Brittney L. Gurda, Sujata Halder |
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| Rok vydání: | 2013 |
| Předmět: |
Models
Molecular Antigenicity Protein Conformation Viral protein viruses Immunology Biology Crystallography X-Ray medicine.disease_cause Microbiology Virus Transduction (genetics) Protein structure Virology Electrochemistry medicine Adeno-associated virus chemistry.chemical_classification Structure and Assembly Dependovirus Molecular biology Amino acid Cell biology chemistry Capsid Insect Science Capsid Proteins |
| Zdroj: | Journal of Virology. 87:11187-11199 |
| ISSN: | 1098-5514 0022-538X |
| DOI: | 10.1128/jvi.00867-13 |
| Popis: | The adeno-associated viruses (AAVs) display differential cell binding, transduction, and antigenic characteristics specified by their capsid viral protein (VP) composition. Toward structure-function annotation, the crystal structure of AAV5, one of the most sequence diverse AAV serotypes, was determined to 3.45-Å resolution. The AAV5 VP and capsid conserve topological features previously described for other AAVs but uniquely differ in the surface-exposed HI loop between βH and βI of the core β-barrel motif and have pronounced conformational differences in two of the AAV surface variable regions (VRs), VR-IV and VR-VII. The HI loop is structurally conserved in other AAVs despite amino acid differences but is smaller in AAV5 due to an amino acid deletion. This HI loop is adjacent to VR-VII, which is largest in AAV5. The VR-IV, which forms the larger outermost finger-like loop contributing to the protrusions surrounding the icosahedral 3-fold axes of the AAVs, is shorter in AAV5, creating a smoother capsid surface topology. The HI loop plays a role in AAV capsid assembly and genome packaging, and VR-IV and VR-VII are associated with transduction and antigenic differences, respectively, between the AAVs. A comparison of interior capsid surface charge and volume of AAV5 to AAV2 and AAV4 showed a higher propensity of acidic residues but similar volumes, consistent with comparable DNA packaging capacities. This structure provided a three-dimensional (3D) template for functional annotation of the AAV5 capsid with respect to regions that confer assembly efficiency, dictate cellular transduction phenotypes, and control antigenicity. |
| Databáze: | OpenAIRE |
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