Srinivas Volety, Raman Bakthisaran, Rao Kunchala Sridhar, Ramakrishna Tangirala, Rao Ch Mohan
Centre for Cellular & Molecular Biology, Hyderabad 500 007, India.
Protein Sci. 2003 Jun;12(6):1262-70. doi: 10.1110/ps.0302003.
Structural perturbation of alpha-crystallin is shown to enhance its molecular chaperone-like activity in preventing aggregation of target proteins. We demonstrate that arginine, a biologically compatible molecule that is known to bind to the peptide backbone and negatively charged side-chains, increases the chaperone-like activity of calf eye lens alpha-crystallin as well as recombinant human alphaA- and alphaB-crystallins. Arginine-induced increase in the chaperone activity is more pronounced for alphaB-crystallin than for alphaA-crystallin. Other guanidinium compounds such as aminoguanidine hydrochloride and guanidine hydrochloride also show a similar effect, but to different extents. A point mutation, R120G, in alphaB-crystallin that is associated with desmin-related myopathy, results in a significant loss of chaperone-like activity. Arginine restores the activity of mutant protein to a considerable extent. We have investigated the effect of arginine on the structural changes of alpha-crystallin by circular dichroism, fluorescence, and glycerol gradient sedimentation. Far-UV CD spectra show no significant changes in secondary structure, whereas near-UV CD spectra show subtle changes in the presence of arginine. Glycerol gradient sedimentation shows a significant decrease in the size of alpha-crystallin oligomer in the presence of arginine. Increased exposure of hydrophobic surfaces of alpha-crystallin, as monitored by pyrene-solubilization and ANS-fluorescence, is observed in the presence of arginine. These results show that arginine brings about subtle changes in the tertiary structure and significant changes in the quaternary structure of alpha-crystallin and enhances its chaperone-like activity significantly. This study should prove useful in designing strategies to improve chaperone function for therapeutic applications.
α-晶状体蛋白的结构扰动被证明可增强其在防止靶蛋白聚集方面的分子伴侣样活性。我们证明,精氨酸是一种已知能与肽主链和带负电荷的侧链结合的生物相容性分子,它能增强小牛眼晶状体α-晶状体蛋白以及重组人αA-和αB-晶状体蛋白的分子伴侣样活性。精氨酸诱导的分子伴侣活性增加对αB-晶状体蛋白比对αA-晶状体蛋白更明显。其他胍类化合物,如盐酸氨基胍和盐酸胍,也显示出类似的效果,但程度不同。αB-晶状体蛋白中与结蛋白相关肌病相关的点突变R120G导致分子伴侣样活性显著丧失。精氨酸在很大程度上恢复了突变蛋白的活性。我们通过圆二色性、荧光和甘油梯度沉降研究了精氨酸对α-晶状体蛋白结构变化的影响。远紫外圆二色光谱显示二级结构没有显著变化,而近紫外圆二色光谱显示在精氨酸存在下有细微变化。甘油梯度沉降显示在精氨酸存在下α-晶状体蛋白寡聚体的大小显著减小。通过芘增溶和ANS荧光监测,在精氨酸存在下观察到α-晶状体蛋白疏水表面的暴露增加。这些结果表明,精氨酸引起α-晶状体蛋白三级结构的细微变化和四级结构的显著变化,并显著增强其分子伴侣样活性。这项研究在设计改善分子伴侣功能以用于治疗应用的策略方面应该是有用的。