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Journal of Virology, April 2007, p. 3645-3648, Vol. 81, No. 7
0022-538X/07/$08.00+0 doi:10.1128/JVI.01778-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Department of Biochemistry and Molecular Biology,1 Department of Microbiology and Immunology, Center for Molecular Virology and Neuroimmunology, Institute for Molecular Medicine and Infectious Disease, Drexel University College of Medicine, 245 N. 15th Street, Philadelphia, Pennsylvania 19102,2 Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 208923
Received 16 August 2006/ Accepted 3 January 2007
The AIDS epidemic continues to spread at an alarming rate worldwide, especially in developing countries. One approach to solving this problem is the generation of anti-human immunodeficiency virus (HIV) compounds with inhibition spectra broad enough to include globally prevailing forms of the virus. We have examined the HIV type 1 (HIV-1) envelope specificity of a recently identified entry inhibitor candidate, HNG-105, using surface plasmon resonance spectroscopy and pseudovirus inhibition assays. The combined results suggest that the HNG-105 molecule may be effective across the HIV-1 subtypes, and they highlight its potential as a lead for developing therapeutic and microbicidal agents to help combat the spread of AIDS.
Published ahead of print on 24 January 2007.
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