Inhibition of HIV-1 reverse transcriptase and protease by phlorotannins from the brown alga Ecklonia cava
Mi-Jeong Ahn, Kee-Dong Yoon, So-Young Min, Ji Suk Lee, Jeong Ha Kim, Tae Gyun Kim, Seung Hee Kim, Nam-Gil Kim, Hoon Huh, Jinwoong Kim, Mi-Jeong Ahn, Kee-Dong Yoon, So-Young Min, Ji Suk Lee, Jeong Ha Kim, Tae Gyun Kim, Seung Hee Kim, Nam-Gil Kim, Hoon Huh, Jinwoong Kim
Abstract
The bioassay-directed isolation of a marine brown alga, Ecklonia cava, afforded four phlorotannin derivatives, eckol (1), 8,8'-bieckol (2), 8,4"'-dieckol (3), and phlorofucofuroeckol A (4). Among these compounds, 2 and 3 exhibited an inhibitory effect on human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) and protease. Specifically, they inhibited the RT more potently than the protease. The inhibitory activity of compound 2 (IC(50), 0.51 microM) against HIV-1 RT was comparable to that of nevirapine (IC(50), 0.28 microM), a reference compound. An enzyme kinetic assay showed that this compound inhibited the RNA-dependent DNA synthesis activity of HIV-1 RT noncompetitively against dUTP/dTTP with a K(i) value of 0.78 microM. With respect to the homopolymeric template/primer, (rA)n(dT)15, 8,8'-bieckol (2) displayed an uncompetitive type of inhibition (K(i), 0.23 microM).
Source: PubMed