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9-(二氰基乙烯基)久洛定与牛脑钙调蛋白的结合

9-(Dicyanovinyl)julolidine binding to bovine brain calmodulin.

作者信息

Iio T, Itakura M, Takahashi S, Sawada S

机构信息

Department of Physics, Faculty of Science, Nagoya University, Aichi.

出版信息

J Biochem. 1991 Apr;109(4):499-502. doi: 10.1093/oxfordjournals.jbchem.a123410.

Abstract

A molecular rotor, 9-(dicyanovinyl)julolidine (DCVJ), is a fluorescent dye whose intramolecular rotation determines its fluorescence yield [Kung, C.E. & Reed, J.K. (1989) Biochemistry 28, 6678-6686]. DCVJ binds to bovine brain calmodulin and emits strong fluorescence. In fluorescence titration experiments, the dissociation constant and the number of binding sites were determined to be 20 +/- 10 microM and 0.7 +/- 0.5 in the presence of Ca2+, and 22 +/- 10 microM and 0.6 +/- 0.5 in the absence of Ca2+, respectively. The fluorescence intensity of bound DCVJ increased 10-fold in the presence of Ca2+ compared to that in the absence of Ca2+. The fluorescence titration curve of DCVJ-calmodulin showed a transition at pCa 6.5. Over the same Ca2+ range, a decrease in molecular ellipticity at 222 nm and an increase in tyrosine fluorescence of calmodulin were observed. These results mean that the conformational change of calmodulin due to the Ca2+ binding induces the microenvironmental change of the DCVJ binding site from the flexible to the rigid state, resulting in inhibition of the intramolecular rotation of DCVJ and an increase in its fluorescence.

摘要

一种分子转子,9-(二氰基亚乙烯基)久洛尼定(DCVJ),是一种荧光染料,其分子内旋转决定了它的荧光产率[Kung, C.E. & Reed, J.K. (1989) Biochemistry 28, 6678 - 6686]。DCVJ与牛脑钙调蛋白结合并发出强烈荧光。在荧光滴定实验中,在有Ca2+存在时,解离常数和结合位点数分别测定为20±10微摩尔和0.7±0.5,在无Ca2+存在时分别为22±10微摩尔和0.6±0.5。与无Ca2+时相比,有Ca2+存在时结合的DCVJ的荧光强度增加了10倍。DCVJ - 钙调蛋白的荧光滴定曲线在pCa 6.5处出现转变。在相同的Ca2+范围内,观察到钙调蛋白在222纳米处的分子椭圆率降低以及酪氨酸荧光增加。这些结果意味着由于Ca2+结合导致的钙调蛋白构象变化引起了DCVJ结合位点微环境从柔性状态到刚性状态的变化,从而导致DCVJ分子内旋转受到抑制并使其荧光增强。

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