Development of a microtiter plate fluorescent assay for inhibition studies on the HTLV-1 and HIV-1 proteinases

被引:30
|
作者
Bagossi, P
Kádas, J
Miklóssy, G
Boross, P
Weber, IT
Tözsér, J
机构
[1] Univ Debrecen, Med & Hlth Sci Ctr, Res Ctr Mol Med, Dept Biochem & Mol Biol, H-4012 Debrecen, Hungary
[2] Georgia State Univ, Dept Biol, Atlanta, GA USA
关键词
HTLV-1; proteinase; HIV-1; oligopeptide substrates; fluorescent assay; substrate specificity; inhibitors;
D O I
10.1016/j.jviromet.2004.03.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The proteinase of human T-cell leukemia virus type-1 (HTLV-1), similar to the proteinase of human immunodeficiency virus type-1 (HIV-1), is a potential target for chemotherapy, since the virus is associated with a number of human diseases. A microtiter plate fluorescent assay was developed for the HTLV-1 and HIV-1 proteinases for direct comparison of the inhibition profiles of the enzymes. It was established that, except for Indinavir, none of the inhibitors designed against the HIV-1 proteinase were able to inhibit the HTLV-1 proteinase in the studied concentration range, while two reduced peptide bond-containing peptides having the sequence of HTLV-1 cleavage sites were inhibitors of the HTLV-1 proteinase. One of these was potent enough to be used for active site titration of the HTLV-1 proteinase. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 93
页数:7
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