Rao S, Orr G A, Chaudhary A G, Kingston D G, Horwitz S B
Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
J Biol Chem. 1995 Sep 1;270(35):20235-8. doi: 10.1074/jbc.270.35.20235.
Photoaffinity labeling methods are being used to define the molecular contacts between taxol and its target protein, tubulin. Our laboratory has demonstrated previously that [3H]3'-(p-azidobenzamido)taxol photolabels the N-terminal 31 amino acids of beta-tubulin (Rao, S., Krauss, N.E., Heerding, J.M., Swindell, C.S., Ringel, I., Orr, G.A., and Horwitz, S.B. (1994) J. Biol. Chem. 269, 3132-3134). The interaction of a second photoaffinity analogue of taxol, [3H]2-(m-azidobenzoyl)taxol, with tubulin has been investigated. This analogue specifically photolabels beta-tubulin and the photolabeling is completed by both taxol and unlabeled 2-(m-azidobenzoyl)-taxol indicating a common binding domain. To identify the site(s) of photoincorporation, [3H]2-(m-azidobenzoyl)taxol-photolabeled beta-tubulin was subjected to sequential cyanogen bromide and tryptic digestions. Radiolabeled peptides were purified by reverse phase high performance liquid chromatography, and amino acid sequencing studies identified a peptide containing amino acid residues 217-231 of beta-tubulin as the major photolabeled domain.
光亲和标记方法正被用于确定紫杉醇与其靶蛋白微管蛋白之间的分子接触。我们实验室先前已证明,[3H]3'-(对叠氮苯甲酰胺基)紫杉醇可光标记β-微管蛋白的N端31个氨基酸(Rao, S., Krauss, N.E., Heerding, J.M., Swindell, C.S., Ringel, I., Orr, G.A., and Horwitz, S.B. (1994) J. Biol. Chem. 269, 3132 - 3134)。对紫杉醇的另一种光亲和类似物[3H]2-(间叠氮苯甲酰基)紫杉醇与微管蛋白的相互作用进行了研究。这种类似物特异性地光标记β-微管蛋白,并且紫杉醇和未标记的2-(间叠氮苯甲酰基)紫杉醇都能完成光标记,这表明存在一个共同的结合结构域。为了确定光掺入的位点,对[3H]2-(间叠氮苯甲酰基)紫杉醇光标记的β-微管蛋白进行了连续的溴化氰和胰蛋白酶消化。通过反相高效液相色谱法纯化放射性标记的肽段,氨基酸测序研究确定含有β-微管蛋白217 - 231位氨基酸残基的肽段是主要的光标记结构域。