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核黄素结合蛋白与核黄素、喹吖因、氯丙嗪及柔红霉素的相互作用。

Interaction of riboflavin binding protein with riboflavin, quinacrine, chlorpromazine and daunomycin.

作者信息

Galat A

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.

出版信息

Int J Biochem. 1988;20(9):1021-9. doi: 10.1016/0020-711x(88)90191-7.

Abstract
  1. circular dichroism and fluorescence measurements were used to study the reversible unfolding of riboflavin-riboflavin binding protein complex. Both methods showed that the complex was unfolded according to the two-state model. 2. The results suggest that riboflavin was strongly bound in the hydrophobic cleft of the protein and that it could not be dislodged by TFE, MeOH or SDS without major unfolding of the unique tertiary structure of the protein. 3. In addition, it has been also shown that quinacrine, chlorpromazine and daunomycin did not form stereospecific complexes with riboflavin binding protein.
摘要
  1. 利用圆二色性和荧光测量研究了核黄素-核黄素结合蛋白复合物的可逆去折叠。两种方法均表明该复合物按照两态模型去折叠。2. 结果表明核黄素紧密结合于蛋白质的疏水裂隙中,并且在不使蛋白质独特的三级结构发生重大去折叠的情况下,TFE、甲醇或十二烷基硫酸钠都无法将其去除。3. 此外,还表明奎纳克林、氯丙嗪和柔红霉素不会与核黄素结合蛋白形成立体特异性复合物。

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