Originally published as Genetics Published Articles Ahead of Print on December 15, 2005.
Genetics, Vol. 172, 1385-1396, March 2006, Copyright © 2006
doi:10.1534/genetics.105.051508
Fold Recognition of the Human Immunodeficiency Virus Type 1 V3 Loop and Flexibility of Its Crown Structure During the Course of Adaptation to a Host
Teruaki Watabe*,1,
Hirohisa Kishino
,
Yoshiyasu Okuhara* and
Yasuhiro Kitazoe*
* Center of Medical Information Science, Kochi University, Kochi 783-8505, Japan and
Laboratory of Biometrics, Graduate School of Agriculture and Life Science, University of Tokyo, Tokyo 113-8657, Japan
1 Corresponding author: Center of Medical Information Science, Kochi University, Kohasu, Oko-cho, Nankoku, Kochi 783-8505, Japan.
E-mail: twatabe-mi{at}umin.ac.jp
The third hypervariable (V3) region of the HIV-1 gp120 protein is responsible for many aspects of viral infectivity. The tertiary structure of the V3 loop seems to influence the coreceptor usage of the virus, which is an important determinant of HIV pathogenesis. Hence, the information about preferred conformations of the V3-loop region and its flexibility could be a crucial tool for understanding the mechanisms of progression from an initial infection to AIDS. Taking into account the uncertainty of the loop structure, we predicted the structural flexibility, diversity, and sequence fitness to the V3-loop structure for each of the sequences serially sampled during an asymptomatic period. Structural diversity correlated with sequence diversity. The predicted crown structure usage implied that structural flexibility depended on the patient and that the antigenic character of the virus might be almost uniform in a patient whose immune system is strong. Furthermore, the predicted structural ensemble suggested that toward the end of the asymptomatic period there was a change in the V3-loop structure or in the environment surrounding the V3 loop, possibly because of its proximity to the gp120 core.
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Copyright © 2006 by the Genetics Society of America.