Wower J, Aymie M, Hixson S S, Zimmermann R A
Department of Biochemistry, University of Massachusetts, Amherst 01003.
Biochemistry. 1989 Feb 21;28(4):1563-7. doi: 10.1021/bi00430a021.
A simple method has been developed for the preparation of 5'-32P-labeled 8-azidoadenosine 3',5'-bisphosphate (p8N3Ap) for use in photoaffinity labeling studies. Irradiation of a complex between p8N3Ap and bovine pancreatic ribonuclease A (RNase A) with light of 300-350 nm led to the covalent attachment of the nucleotide to the enzyme. RNase A could also be labeled in the dark with prephotolyzed p8N3Ap. In either case, the nucleotide reacted with the same tryptic peptide, encompassing amino acids 67-85 of the protein. The site of labeling was determined to be either Thr-78 or Thr-82, both of which are close to or at the pyrimidine binding site of the enzyme. This result is consistent with recent nuclear magnetic resonance and X-ray studies which indicate that 8-substituted adenine nucleotides interact with the pyrimidine binding site of RNase A.
已开发出一种简单方法,用于制备用于光亲和标记研究的5'-32P标记的8-叠氮腺苷3',5'-二磷酸(p8N3Ap)。用300 - 350 nm的光照射p8N3Ap与牛胰核糖核酸酶A(RNase A)之间的复合物,导致核苷酸与该酶共价结合。RNase A也可以在黑暗中用预光解的p8N3Ap进行标记。在这两种情况下,核苷酸都与相同的胰蛋白酶肽段反应,该肽段包含蛋白质的67 - 85位氨基酸。标记位点确定为Thr-78或Thr-82,这两个位点都靠近或位于该酶的嘧啶结合位点。这一结果与最近的核磁共振和X射线研究一致,这些研究表明8-取代的腺嘌呤核苷酸与RNase A的嘧啶结合位点相互作用。