Porphyrins affect the self-assembly of tubulin in solution

被引:2
作者
Valdez, Rolando [1 ]
Johnson, Eric M. [1 ]
Belcher, John A. [1 ]
Fuini, John F., III [1 ]
Brancaleon, Lorenzo [1 ]
机构
[1] Univ Texas San Antonio, Dept Phys & Astron, San Antonio, TX 78249 USA
关键词
Microtubules; Porphyrins; Electron microscopy; Binding; ALPHA-BETA-TUBULIN; IN-VITRO; BINDING; SITE; GTP; MICROTUBULES; INHIBITION; PACLITAXEL; COLCHICINE; KINETICS;
D O I
10.1016/j.bpc.2009.09.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Self-assembly of tubulin heterodimers in solution has been studied in the past to predict the effects that ligands and/or conformational changes have on the formation of tubulin filaments. Self-assembly of tubulin in solution has produced formations similar to cellular microtubules (MTs). The present study reports on the effects that two porphyrins (protoporphyrin IX, PPIX and tetrakis(4-sulfonatophenyl)porphyrin, TPPS) produce on the self-assembly of tubulin alpha,beta-heterodimers in buffer solution. The study shows that, when incubated simultaneously with MT-stabilizing ligands (i.e., paclitaxel and guanosine triphosphate, GTP), porphyrins do not affect the ability of tubulin to form MT. However, if paclitaxel and GTP are added after tubulin has been allowed to self-assemble in the presence of either porphyrin, the ability to form MT-like structures is reduced or suppressed. We suggest that this effect is due to the formation of porphyrin-mediated aggregates that cannot be broken or elongated by the addition of GTP or paclitaxel. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:98 / 104
页数:7
相关论文
共 43 条
[1]   How Taxol® stabilises microtubule structure [J].
Amos, LA ;
Löwe, J .
CHEMISTRY & BIOLOGY, 1999, 6 (03) :R65-R69
[2]   HOW DOES TAXOL STABILIZE MICROTUBULES [J].
ARNAL, I ;
WADE, RH .
CURRENT BIOLOGY, 1995, 5 (08) :900-908
[3]   MICROTUBULE DYNAMICS [J].
AVILA, J .
FASEB JOURNAL, 1990, 4 (15) :3284-3290
[4]   GAMMA-TUBULIN DISTRIBUTION IN THE NEURON - IMPLICATIONS FOR THE ORIGINS OF NEURITIC MICROTUBULES [J].
BAAS, PW ;
JOSHI, HC .
JOURNAL OF CELL BIOLOGY, 1992, 119 (01) :171-178
[5]   Identification of cysteine 354 of beta-tubulin as part of the binding site for the A ring of colchicine [J].
Bai, RL ;
Pei, XF ;
Boye, O ;
Getahun, Z ;
Grover, S ;
Bekisz, J ;
Nguyen, NY ;
Brossi, A ;
Hamel, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (21) :12639-12645
[6]   Sulfonamide drugs binding to the colchicine site of tubulin: Thermodynamic analysis of the drug-tubulin interactions by isothermal titration calorimetry [J].
Banerjee, M ;
Poddar, A ;
Mitra, G ;
Surolia, A ;
Owa, T ;
Bhattacharyya, B .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (02) :547-555
[7]   STEADY-STATE AND TIME-RESOLVED SPECTROSCOPIC STUDIES ON THE HEMATOPORPHYRIN LIPOPROTEIN COMPLEX [J].
BELTRAMINI, M ;
FIREY, PA ;
RICCHELLI, F ;
RODGERS, MAJ ;
JORI, G .
BIOCHEMISTRY, 1987, 26 (21) :6852-6858
[8]   Lysosomes and microtubules as targets for photochemotherapy of cancer [J].
Berg, K ;
Moan, J .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 65 (03) :403-409
[9]   MITOTIC INHIBITION BY PHENYLPORPHINES AND TETRASULFONATED ALUMINUM PHTHALOCYANINE IN COMBINATION WITH LIGHT [J].
BERG, K ;
MOAN, J .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1992, 56 (03) :333-339
[10]   THE UNPOLYMERIZED FORM OF TUBULIN IS THE TARGET FOR MICROTUBULE INHIBITION BY PHOTOACTIVATED TETRA(4-SULFONATOPHENYL) PORPHINE [J].
BERG, K .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1135 (02) :147-153