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先天性类脂质性肾上腺增生中类固醇生成急性调节蛋白(StAR)的错误折叠。

Incorrect folding of steroidogenic acute regulatory protein (StAR) in congenital lipoid adrenal hyperplasia.

作者信息

Bose H S, Baldwin M A, Miller W L

机构信息

Department of Pediatrics, University of California, San Francisco 94143-0978, USA.

出版信息

Biochemistry. 1998 Jul 7;37(27):9768-75. doi: 10.1021/bi980588a.

Abstract

Steroidogenic acute regulatory protein (StAR) rapidly stimulates the movement of cholesterol into adrenal and gonadal mitochondria to mediate the acute steroidogenic response; StAR mutations cause potentially lethal congenital lipoid adrenal hyperplasia (lipoid CAH). Bacterially expressed wild-type StAR and four amino acid replacement/deletion mutants that cause lipoid CAH were purified to apparent homogeneity. Sedimentation equilibrium ultracentrifugation showed that all five proteins were monomeric and fit a globular protein model of the correct molecular mass. Circular dichroism (CD) spectra of both the wild-type and mutants showed minima near 208 and 222 nm, confirming the presence of substantial alpha-helical structure. However, subtle differences in the CD signals of the wild-type and mutants in the far-UV and stronger differences in near-UV indicated differences in protein folding. The amide I and II bands in the 1400-1700 cm-1 region of Fourier transform infrared spectra showed that the proteins fell into two groups. The wild-type and a partially active conservative mutant were predominantly alpha-helical with some intramolecular beta-sheet. By contrast, three mutants that lost charged residues retained much of their alpha-helical structure, but also tended to form intermolecular beta-sheets. Urea at 2.0 or 4.0 M had less effect on the CD spectrum of the wild-type than of the mutants, particularly those having lost a charged residue; 50 mM guanidinium hydrochloride did not alter the CD spectrum of the wild-type, but elicited dramatic changes to the secondary structure in all four mutants. Despite this, thermal melting curves of the mutant proteins in 50 mM guanidinium hydrochloride showed surprising stability, even exceeding that of the wild-type protein. These data suggest that the StAR amino acid replacement mutants that cause lipoid CAH are inactive because of fairly gross errors in protein folding, probably due to the loss of salt bridges that stabilize the tertiary structure.

摘要

类固醇生成急性调节蛋白(StAR)能迅速刺激胆固醇转运至肾上腺和性腺线粒体,从而介导急性类固醇生成反应;StAR突变会导致具有潜在致死性的先天性类脂性肾上腺增生症(类脂性CAH)。将细菌表达的野生型StAR以及导致类脂性CAH的四个氨基酸替换/缺失突变体纯化至表观均一。沉降平衡超速离心显示,所有这五种蛋白质均为单体,且符合正确分子量的球状蛋白质模型。野生型和突变体的圆二色性(CD)光谱在208和222nm附近均出现最小值,证实存在大量α-螺旋结构。然而,野生型和突变体在远紫外区的CD信号存在细微差异,近紫外区差异更明显,这表明蛋白质折叠存在差异。傅里叶变换红外光谱在1400 - 1700cm-1区域的酰胺I和II带显示,这些蛋白质可分为两组。野生型和一个部分活性的保守突变体主要为α-螺旋结构,并含有一些分子内β-折叠。相比之下,三个失去带电残基的突变体虽保留了大部分α-螺旋结构,但也倾向于形成分子间β-折叠。2.0或4.0M的尿素对野生型CD光谱的影响小于对突变体的影响,尤其是那些失去带电残基的突变体;50mM盐酸胍不会改变野生型的CD光谱,但会引起所有四个突变体二级结构的显著变化。尽管如此,突变蛋白在50mM盐酸胍中的热熔解曲线显示出惊人的稳定性,甚至超过野生型蛋白。这些数据表明,导致类脂性CAH的StAR氨基酸替换突变体无活性是由于蛋白质折叠存在相当严重的错误,这可能是由于稳定三级结构的盐桥缺失所致。

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