Takemoto L, Emmons T
Division of Biology, Kansas State University, Manhattan 66506.
Invest Ophthalmol Vis Sci. 1990 Jul;31(7):1348-52.
Antisera have been made to synthetic peptides that correspond to eight different regions of the alpha A molecule. Together with a solid phase radioimmunoassay, these antisera have been used to quantitatively assess binding to enriched alpha crystallin preparations from six different cataractous and six different normal lenses. Seven of the eight antisera show no difference in binding to alpha crystallin from cataractous versus normal lenses, whereas the antiserum directed against the alpha A sequence 120-130 shows a statistically significant decrease in binding to the alpha crystallin from cataractous lenses. Together, these studies demonstrate the feasibility of using antipeptide sera as probes of polypeptide changes during cataractogenesis and suggest that the region of the alpha A crystallin molecule encompassing residues 120-300 may undergo covalent and/or noncovalent structural modification during the process of opacification in the human senile lens.
已针对与αA分子八个不同区域相对应的合成肽制备了抗血清。这些抗血清与固相放射免疫测定法一起,用于定量评估与来自六个不同白内障晶状体和六个不同正常晶状体的富集α晶状体蛋白制剂的结合。八个抗血清中的七个在与白内障晶状体和正常晶状体的α晶状体蛋白结合方面没有差异,而针对αA序列120 - 130的抗血清显示与白内障晶状体的α晶状体蛋白结合在统计学上有显著下降。总之,这些研究证明了使用抗肽血清作为白内障形成过程中多肽变化探针的可行性,并表明αA晶状体蛋白分子中包含120 - 300残基的区域在人类老年性晶状体混浊过程中可能经历共价和/或非共价结构修饰。