Sawada T, Kobayashi H, Hashimoto Y, Iwasaki S
Institute of Applied Microbiology, University of Tokyo, Japan.
Biochem Pharmacol. 1993 Apr 6;45(7):1387-94. doi: 10.1016/0006-2952(93)90036-v.
The rhizoxin (RZX)-binding site on porcine brain tubulin was investigated by photoaffinity labeling with the 5-azido-1-naphthalene sulfonyl (azidodansyl) derivative of RZX, nor-rhizoxin-22-al-5'-azidonaphthalene-1'-sulfonylhydrazo ne (azidodansylrhizoxin: Adan-RZX). Upon ultraviolet irradiation, Adan-RZX generates a highly reactive nitrene, which irreversibly binds to an amino acid residue(s) near the RZX-binding site. The label was found to be on beta-tubulin. Enzymatic digestion of the labeled tubulin generated only one major fluorescent peak on C18 reverse phase HPLC analysis. The labeled site(s) was mapped by using various combinations of highly specific peptidases in succession. That is, the labeled fragment generated by the first peptidase was purified by HPLC and exposed to a second peptidase; if the retention time in HPLC changed after the second digestion, the fragment generated in the first digestion must have contained the recognition site(s) of the second enzyme. From the results of these successive digestions and the known polypeptide sequences, we could identify the labeled fragment as Met-363-Lys-379 of beta-tubulin. This peptidase combination technique should be widely applicable.
通过用根霉素(RZX)的5-叠氮基-1-萘磺酰基(叠氮丹磺酰基)衍生物、去甲根霉素-22-醛-5'-叠氮萘-1'-磺酰腙(叠氮丹磺酰基根霉素:Adan-RZX)进行光亲和标记,研究了猪脑微管蛋白上的根霉素(RZX)结合位点。在紫外线照射下,Adan-RZX产生一种高活性氮烯,它不可逆地与RZX结合位点附近的一个或多个氨基酸残基结合。发现标记物位于β-微管蛋白上。对标记的微管蛋白进行酶消化后,在C18反相高效液相色谱分析中仅产生一个主要荧光峰。通过连续使用各种高特异性肽酶的组合来定位标记位点。也就是说,由第一种肽酶产生的标记片段通过高效液相色谱纯化,然后暴露于第二种肽酶;如果在第二次消化后高效液相色谱中的保留时间发生变化,那么第一次消化产生的片段必定包含第二种酶的识别位点。根据这些连续消化的结果和已知的多肽序列,我们可以将标记片段鉴定为β-微管蛋白的Met-363-Lys-379。这种肽酶组合技术应该具有广泛的适用性。