Michellamine alkaloids inhibit protein kinase C

被引:13
作者
White, EL
Chao, WR
Ross, LJ
Borhani, DW
Hobbs, PD
Upender, V
Dawson, MI
机构
[1] So Res Inst, Dept Biochem, Birmingham, AL 35205 USA
[2] So Res Inst, Dept Organ Chem, Birmingham, AL 35205 USA
[3] SRI Int, Menlo Park, CA 94025 USA
关键词
michellamine; protein kinase C;
D O I
10.1006/abbi.1999.1145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Michellamines A, B, and C have shown antiviral activitity against HIV-1 and HIV-2 in cell culture, They act in a complex manner by at least two reported antiviral mechanisms, inhibition of HIV reverse transcriptase and inhibition of HIV-induced cellular fusion, On the basis of their structural similarity to other protein kinase C (PKC) inhibitors, we have investigated another possible mechanism-inhibition of PKC, The michellamines were found to inhibit rat brain PKC with IC50 values in the 15-35 mu M range. Michellamine B was a noncompetitive PKC inhibitor with respect to ATP with a K-i value of 4-6 mu M, whereas mixed-type inhibition was observed when the peptide concentration was varied, Michellamine B inhibited the kinase domain of PKC similarly. These results indicate that the michellamines bind to the PKC kinase domain and not its regulatory domain, Molecular modeling showed that all three michellamines can bind in the active site cleft of the PKC kinase domain, to block both the ATP and the peptide substrate subsites, (C) 1999 Academic Press.
引用
收藏
页码:25 / 30
页数:6
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