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Journal of Virology, July 2003, p. 7527-7538, Vol. 77, No. 13
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.13.7527-7538.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Importance of Vp1 Calcium-Binding Residues in Assembly, Cell Entry, and Nuclear Entry of Simian Virus 40

Peggy P. Li,1 Akira Naknanishi,1 Mary A. Tran,1 Ken-Ichiro Ishizu,2 Masaaki Kawano,2 Martin Phillips,3 Hiroshi Handa,4 Robert C. Liddington,5 and Harumi Kasamatsu1*

Department of Molecular, Cell and Developmental Biology and Molecular Biology Institute,1 Department of Chemistry and Biochemistry, University of California at Los Angeles, Los Angeles, California 90095,3 Frontier Collaborative Research Center,4 Faculty of Bioscience and Biotechnology, Tokyo Institute of Technology, Midori-ku, Yokohama 226-8501, Japan,2 The Burnham Institute, La Jolla, California 920375

Received 8 January 2003/ Accepted 4 April 2003

For polyomaviruses, calcium ions are known to be essential for virion integrity and for the assembly of capsid structures. To define the role of calcium ions in the life cycle of the virus, we analyzed simian virus 40 (SV40) mutants in which structurally deduced calcium-binding amino acids of Vp1 were mutated singly and in combination. Our study provides evidence that calcium ions mediate not only virion assembly but also the initial infection processes of cell entry and nuclear entry. Mutations at Glu48, Glu157, Glu160, Glu216, and/or Glu330 are correlated with different extents of packaging defects. The low packaging ability of mutant E216R suggests the need to position the Glu216 side chain for proper virion formation. All other mutants selected for further analysis produced virus-like particles (VLPs) but were poorly infectious. The VLPs of mutant E330K could not attach to or enter the cell, and mutant E157A-E160A and E216K VLPs entered the cell but failed to enter the nucleus, apparently as a result of premature VLP dissociation. Our results show that five of the seven acidic side chains at the two calcium-binding sites—Glu48 and Glu330 (site 1), Glu157 and Glu160 (site 2), and Glu216 (both sites)—are important for SV40 infection. We propose that calcium coordination imparts not only stability but also structural flexibility to the virion, allowing the acquisition or loss of the ion at the two sites to control virion formation in the nucleus, as well as virion structural alterations at the cell surface and in the cytoplasm early during infection.


* Corresponding author. Mailing address: Molecular Biology Institute, 456 Boyer Hall, University of California at Los Angeles, 611 E. Charles E. Young Dr., Box 951570, Los Angeles, CA 90095-1570. Phone: (310) 825-3048. Fax: (310) 206-7286. E-mail: harumi_K{at}mbi.ucla.edu.


Journal of Virology, July 2003, p. 7527-7538, Vol. 77, No. 13
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.13.7527-7538.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




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