3J4P

Electron Microscopy Analysis of a Disaccharide Analog complex Reveals Receptor Interactions of Adeno-Associated Virus

Summary for 3J4P

• Entry DOI: 10.2210/pdb3j4p/pdb
• EMDB information: 5681
• Related PRD ID: PRD_900013
• Descriptor: Capsid protein VP1, 1,3,4,6-tetra-O-sulfo-beta-D-fructofuranose-(2-1)-2,3,4,6-tetra-O-sulfonato-alpha-D-glucopyranose, SODIUM ION, ... (5 entities in total)
• Functional Keywords: virus cell-receptor interaction, virus
• Biological source: Adeno-associated virus
• Total number of polymer chains: 1
• Total formula weight: 59607.63

Authors

Xie, Q.,Chapman, M.S. (deposition date: 2013-09-10, release date: 2013-10-16, Last modification date: 2024-02-21)

Primary citation

Xie, Q.,Spilman, M.,Meyer, N.L.,Lerch, T.F.,Stagg, S.M.,Chapman, M.S.
Electron microscopy analysis of a disaccharide analog complex reveals receptor interactions of adeno-associated virus.
J.Struct.Biol., 184:129-135, 2013

PubMed Abstract: Mechanistic studies of macromolecular complexes often feature X-ray structures of complexes with bound ligands. The attachment of adeno-associated virus (AAV) to cell surface glycosaminoglycans (GAGs) is an example that has not proven amenable to crystallography, because the binding of GAG analogs disrupts lattice contacts. The interactions of AAV with GAGs are of interest in mediating the cell specificity of AAV-based gene therapy vectors. Previous electron microscopy led to differing conclusions on the exact binding site and the existence of large ligand-induced conformational changes in the virus. Conformational changes are expected during cell entry, but it has remained unclear whether the electron microscopy provided evidence of their induction by GAG-binding. Taking advantage of automated data collection, careful processing and new methods of structure refinement, the structure of AAV-DJ complexed with sucrose octasulfate is determined by electron microscopy difference map analysis to 4.8Å resolution. At this higher resolution, individual sulfate groups are discernible, providing a stereochemical validation of map interpretation, and highlighting interactions with two surface arginines that have been implicated in genetic studies. Conformational changes induced by the SOS are modest and limited to the loop most directly interacting with the ligand. While the resolution attainable will depend on sample order and other factors, there are an increasing number of macromolecular complexes that can be studied by cryo-electron microscopy at resolutions beyond 5Å, for which the approaches used here could be used to characterize the binding of inhibitors and other small molecule effectors when crystallography is not tractable.

PubMed: 24036405
DOI: 10.1016/j.jsb.2013.09.004

Experimental method

ELECTRON MICROSCOPY (4.8 Å)