Structural intermediates in the assembly of taxoid-induced microtubules and GDP-tubulin double rings: Time-resolved X-ray scattering

被引:25
作者
Diaz, JF
Andreu, JM
Diakun, G
TownsAndrews, E
Bordas, J
机构
[1] CSIC,CTR INVEST BIOL,E-28006 MADRID,SPAIN
[2] DARESBURY LAB,WARRINGTON WA4 4AD,CHESHIRE,ENGLAND
关键词
D O I
10.1016/S0006-3495(96)79809-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We have studied the self-association reactions of purified GDP-liganded tubulin into double rings and taxoid-induced microtubules, employing synchrotron time-resolved x-ray solution scattering. The experimental scattering profiles have been interpreted by reference to the known scattering profiles to 3 nm resolution and to the low-resolution structures of the tubulin dimer, tubulin double rings, and microtubules, and by comparison with oligomer models and model mixtures. The time courses of the scattering bands corresponding to the different structural features were monitored during the assembly reactions under varying biochemical conditions, GDP-tubulin essentially stays as a dimer at low Mg2+ ion activity, in either the absence or presence of taxoid. Upon addition of the divalent cations, it associates into either double-ring aggregates or taxoid-induced microtubules by different pathways. Both processes have the formation of small linear (short protofilament-like) tubulin oligomers in common, Tubulin double-ring aggregate formation, which is shown by x-ray scattering to be favored in the GDP- versus the GTP-liganded protein, can actually block microtubule assembly, The tubulin self-association leading to double rings, as determined by sedimentation velocity, is endothermic, The formation of the double-ring aggregates from oligomers, which involves additional intermolecular contacts, is exothermic, as shown by x-ray and light scattering, Microtubule assembly can be initiated from GDP-tubulin dimers or oligomers, Under fast polymerization conditions, after a short lag time, open taxoid-induced microtubular sheets have been clearly detected (monitored by the central scattering and the maximum corresponding to the J(n) Bessel function), which slowly close into microtubules (monitored by the appearance of their characteristic J(0), J(3), and J(n-3) Bessel function maxima), This provides direct evidence for the bidimensional assembly of taxoid-induced microtubule polymers in solution and argues against helical growth, The rate of microtubule formation was increased by the same factors known to enhance taxoid-induced microtubule stability. The results suggest that taxoids induce the accretion of the existing Mg2+-induced GDP-tubulin oligomers, thus forming small bidimensional polymers that are necessary to nucleate the microtubular sheets, possibly by binding to or modifying the lateral interaction sites between tubulin dimers.
引用
收藏
页码:2408 / 2420
页数:13
相关论文
共 58 条
[1]  
AMOS LA, 1974, J CELL SCI, V14, P523
[2]   A SYNCHROTRON X-RAY-SCATTERING CHARACTERIZATION OF PURIFIED TUBULIN AND OF ITS EXPANSION INDUCED BY MILD DETERGENT BINDING [J].
ANDREU, JM ;
DEANCOS, JG ;
STARLING, D ;
HODGKINSON, JL ;
BORDAS, J .
BIOCHEMISTRY, 1989, 28 (09) :4036-4040
[3]  
ANDREU JM, 1994, J BIOL CHEM, V269, P31785
[4]   LOW RESOLUTION STRUCTURE OF MICROTUBULES IN SOLUTION - SYNCHROTRON X-RAY-SCATTERING AND ELECTRON-MICROSCOPY OF TAXOL-INDUCED MICROTUBULES ASSEMBLED FROM PURIFIED TUBULIN IN COMPARISON WITH GLYCEROL AND MAP-INDUCED MICROTUBULES [J].
ANDREU, JM ;
BORDAS, J ;
DIAZ, JF ;
DEANCOS, JG ;
GIL, R ;
MEDRANO, FJ ;
NOGALES, E ;
PANTOS, E ;
TOWNSANDREWS, E .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 226 (01) :169-184
[5]   MICROTUBULE STRUCTURE AT 18-A RESOLUTION [J].
BEESE, L ;
STUBBS, G ;
COHEN, C .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 194 (02) :257-264
[6]  
BOLLAG DM, 1995, CANCER RES, V55, P2325
[7]   STAGES OF TUBULIN ASSEMBLY AND DISASSEMBLY STUDIED BY TIME-RESOLVED SYNCHROTRON X-RAY-SCATTERING [J].
BORDAS, J ;
MANDELKOW, EM ;
MANDELKOW, E .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 164 (01) :89-135
[8]   TAU-PROTEIN BINDS TO MICROTUBULES THROUGH A FLEXIBLE ARRAY OF DISTRIBUTED WEAK SITES [J].
BUTNER, KA ;
KIRSCHNER, MW .
JOURNAL OF CELL BIOLOGY, 1991, 115 (03) :717-730
[9]   STRUCTURE OF GROWING MICROTUBULE ENDS - 2-DIMENSIONAL SHEETS CLOSE INTO TUBES AT VARIABLE RATES [J].
CHRETIEN, D ;
FULLER, SD ;
KARSENTI, E .
JOURNAL OF CELL BIOLOGY, 1995, 129 (05) :1311-1328
[10]   HYDRODYNAMIC ANALYSIS OF TUBULIN DIMER AND DOUBLE RINGS [J].
DELATORRE, JG ;
ANDREU, JM .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 238 (02) :223-225