Carboxyflavins, novel inhibitors of Taq DNA polymerase

被引:0
作者
Mizushina, Y
Ueno, T
Goto, Y
Isobe, Y
Sako, M
Fujita, T
Hirota, K
Hayashi, H
Sakaguchi, K
机构
[1] Tokyo Univ Sci, Dept Appl Biol Sci, Fac Sci & Technol, Noda, Chiba 2788510, Japan
[2] Japan Energy Co, Pharmaceut & Biotechnol Lab, Toda, Saitama 3358502, Japan
[3] Gifu Pharmaceut Univ, Med Chem Lab, Gifu 5028585, Japan
关键词
Taq DNA polymerase; polymerase chain reaction; enzyme inhibitor; carboxyflavins;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Carboxyflavins were found to be potent selective inhibitors of Tag DNA polymerase in a polymerase chain reaction. The inhibitions were dose-dependent, and complete inhibitions were observed at the concentration of 3.0 mu M Carboxyflavins were much less, or not sensitive to the DNA polymerases tested such as calf thymus DNA polymerase alpha, rat DNA polymerase beta, human immunodeficiency virus type 1 reverse transcriptase, the Klenow Fragment of E. coli DNA polymerase I and T4 DNA polymerase. To our knowledge, there is no other report of an agent that selectively inhibits only a thermophilic polymerase. Interestingly, the carboxy-flavins were able to prevent DNA synthesis in the murine lymphoid leukemia cell line L1210 in vitro; almost complete inhibitory levels were achieved in the range of less than 10 mu M.
引用
收藏
页码:283 / 286
页数:4
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