Andreu J M, Gorbunoff M J, Medrano F J, Rossi M, Timasheff S N
Centro de Investigaciones Biologicas, Consejo Superior de Investigaciones Cientificas, Madrid, Spain.
Biochemistry. 1991 Apr 16;30(15):3777-86. doi: 10.1021/bi00229a027.
The limits of structural variation of the substituent in position 4' of ring C' of biphenyl colchicine analogues (ring C in colchicine) were probed by the synthesis of a number of analogues and the examination of their binding to tubulin and its consequences. Binding was found to require the location in three-dimensional space of the oxygen in the 4'-substituent at a locus not far distant from those of the colchicine ring C oxygens. All those analogues that bind to the colchicine site of tubulin induced the GTPase activity and inhibited microtubule assembly, those containing a carbonyl group substoichiometrically and the others stoichiometrically. A similar relation was found for the induction of the abnormal polymerization of the colchicine analogue-tubulin complex, with methoxy-containing compounds requiring a higher temperature to induce the polymerization. A concerted analysis of the binding thermodynamics of colchicine and its various analogues has shown full consistency with the previously proposed two-step binding pathway that involves two nonidentical binding moieties in the ligand [Andreu, J. M., & Timasheff, S. N. (1982) Biochemistry 21, 534-543]. Comparison of the binding parameters of colchicine, its des(ring B) analogue (MTC), and ring A and C compounds individually with the thermodynamic parameters deduced for the first steps of the bindings of colchicine and MTC [Engelborghs, Y., & Fitzgerald, T. J. (1987) J. Biol. Chem. 262, 5204-5209] have led to the conclusion that binding can occur by two pathways leading to the identical product. In the first pathway, ring A binds first; this is followed by a rate-determining thermodynamically indifferent reaction (protein conformation change), and finally a rapid binding of ring C. In the second pathway, the events are the same except that the order of binding of the rings is reversed. Colchicine, due to the steric hindrance of ring B, can follow only the second pathway. For MTC, both kinetic pathways are open and binding may be initiated by random first contact of either ring A or ring C.
通过合成一系列联苯秋水仙碱类似物(秋水仙碱中的C环)并检测它们与微管蛋白的结合情况及其后果,探究了C'环4'位取代基结构变异的限度。发现结合需要4'-取代基中的氧在三维空间中的位置与秋水仙碱C环氧的位置相距不远。所有与微管蛋白秋水仙碱位点结合的类似物都能诱导GTP酶活性并抑制微管组装,含羰基的类似物以亚化学计量诱导,其他的则以化学计量诱导。对于秋水仙碱类似物 - 微管蛋白复合物异常聚合的诱导也发现了类似关系,含甲氧基的化合物需要更高温度来诱导聚合。对秋水仙碱及其各种类似物结合热力学的协同分析表明,与先前提出的涉及配体中两个不同结合部分的两步结合途径完全一致[安德鲁,J.M.,& 蒂马舍夫,S.N.(1982年)《生物化学》21,534 - 543]。将秋水仙碱、其去(B环)类似物(MTC)以及A环和C环化合物的结合参数分别与从秋水仙碱和MTC结合第一步推导的热力学参数进行比较[恩格尔博格斯,Y.,& 菲茨杰拉德,T.J.(1987年)《生物化学杂志》262,5204 - 5209],得出结论:结合可通过两条途径发生,产生相同产物。在第一条途径中,A环先结合;随后是一个速率决定的热力学中性反应(蛋白质构象变化),最后是C环的快速结合。在第二条途径中,事件相同,只是环的结合顺序相反。由于B环的空间位阻,秋水仙碱只能遵循第二条途径。对于MTC,两条动力学途径都是开放的,结合可能由A环或C环的随机首次接触引发。