Gordon A S, Milfay D, Diamond I
Proc Natl Acad Sci U S A. 1983 Oct;80(19):5862-5. doi: 10.1073/pnas.80.19.5862.
A photoaffinity ATP ligand is used to identify the protein kinase present in acetylcholine receptor-enriched membranes from Torpedo californica. Incubation of these membranes with 8-azido-[alpha-32P]ATP and subsequent irradiation with UV light resulted in covalent labeling of a major band of Mr 43,000. Alkali-stripped membranes that show a selective reduction in the Mr 43,000 polypeptide also show a corresponding reduction in incorporation of photoaffinity label. In addition, the neutralized alkaline extract also showed one band at Mr 43,000 when labeled with the photoaffinity ligand. After alkali extraction, endogenous protein kinase activity decreased in the membranes in proportion to the loss of Mr 43,000 peptide. Moreover, the alkaline extract was able to phosphorylate casein in an exogenous assay system. These results suggest that a Mr 43,000 polypeptide in acetylcholine receptor-enriched membranes is the acetylcholine receptor kinase.
一种光亲和性ATP配体被用于鉴定来自加州电鳐富含乙酰胆碱受体的膜中存在的蛋白激酶。将这些膜与8-叠氮基-[α-³²P]ATP一起孵育并随后用紫外光照射,导致了一条分子量为43,000的主要条带的共价标记。显示分子量为43,000的多肽选择性减少的碱洗脱膜,其光亲和性标记的掺入也相应减少。此外,用该光亲和性配体标记时,中和后的碱性提取物在分子量43,000处也显示出一条条带。碱提取后,膜中的内源性蛋白激酶活性与分子量为43,000的肽段的损失成比例下降。此外,碱性提取物能够在外源测定系统中使酪蛋白磷酸化。这些结果表明,富含乙酰胆碱受体的膜中分子量为43,000的多肽是乙酰胆碱受体激酶。