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Cryoelectron microscopy of protein IX-modified adenoviruses suggests a new position for the C terminus of protein IX
被引:27
作者:
Marsh, Michael P.
Campos, Samuel K.
Baker, Matthew L.
Chen, Christopher Y.
Chiu, Wah
Barry, Michael A.
机构:
[1] Baylor Coll Med, Program Struct & Computat Biol & Mol Biophys, Houston, TX 77030 USA
[2] Baylor Coll Med, Natl Ctr Macromol Imaging, Verna & Marrs McLean Dept Biochem & Mol Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Immunol, Houston, TX 77030 USA
[5] Baylor Coll Med, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[6] Rice Univ, Dept Bioengn, Houston, TX 77251 USA
[7] Rice Univ, Dept Biochem & Cell Biol, Houston, TX 77251 USA
[8] Mayo Clin, Dept Internal Med, Div Infect Dis, Translat Immunovirol Program, Rochester, MN USA
关键词:
D O I:
10.1128/JVI.01471-06
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Recombinant human adenovirus is a useful gene delivery vector for clinical gene therapy. Minor capsid protein IX of adenovirus has been of recent interest since multiple studies have shown that modifications can be made to its C terminus to alter viral tropism or add molecular tags and/or reporter proteins. We examined the structure of an engineered adenovirus displaying the enhanced green fluorescent protein (EGFP) fused to the C terminus of protein IX. Cryoelectron microscopy and reconstruction localized the C-terminal EGFP fusion between the H2 hexon and the H4 hexon, positioned between adjacent facets, directly above the density previously assigned as protein IIIa. The original assignment of IIIa was based largely on indirect evidence, and the data presented herein support the reassignment of the IIIa density as protein IX.
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页码:11881 / 11886
页数:6
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