FEBS Letters | |
MAP 30: a new inhibitor of HIV‐1 infection and replication | |
Lee-Huang, Sylvia5  Huang, Philip L.3  Chen, Hao-Chia4  Huang, Henry I.3  Kung, Hsiang-fu2  Huang, Paul L.3  Huang, Peter3  Nara, Peter L.1  | |
[1] Laboratory of Tumor Cell Biology, National Cancer Institute-Frederick Cancer Research Facility, Frederick, MD 21701, USA;Laboratory of Biochemical Physiology, National Cancer Institute-Frederick Cancer Research Facility, Frederick, MD 21701, USA;American Biosciences, New York, NY 10021, USA;Endocrinology and Reproduction Research Branch, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA;Department of Biochemistry, New York University School of Medicine, New York, NY 10016, USA | |
关键词: Plant protein; Antiviral agent; AIDS; | |
DOI : 10.1016/0014-5793(90)80438-O | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
A new inhibitor of human immunodeficiency virus (HIV) has been isolated and purified to homogeneity from the seeds and fruits of the Momordica charantia. This compound, MAP 30 (Momordica Anti-HIV Protein), is a basic protein of about 30 kDa. It exhibits dose-dependent inhibition of cell-free HIV-1 infection and replication as measured by: (i) quantitative focal syncytium formation on CEM-ss monolayers; (II) viral core protein p24 expression; and (iii) viral-associated reverse transcriptase (RT) activity in HIV-1 infected H9 cells. The doses required for 50% inhibition (ID50) in these assays were 0.83, 0.22 and 0.33 nM, respectively. No cytotoxic or cytostatic effects were found under the assay conditions. These data suggest that MAP 30 may be a useful therapeutic agent in the treatment of HIV-1 infections. The sequence of the N-terminal 44 amino acids of MAP 30 has been determined.
【 授权许可】
Unknown
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