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1
Participation of guanine nucleotides in nucleation and elongation steps of microtubule assembly.鸟嘌呤核苷酸在微管组装的成核和延伸步骤中的参与。
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5475-9. doi: 10.1073/pnas.76.11.5475.
2
Microtubule elongation and guanosine 5'-triphosphate hydrolysis. Role of guanine nucleotides in microtubule dynamics.微管延长与鸟苷5'-三磷酸水解。鸟嘌呤核苷酸在微管动力学中的作用。
Biochemistry. 1987 Jul 14;26(14):4428-37. doi: 10.1021/bi00388a036.
3
Mechanism of GTP hydrolysis in tubulin polymerization: characterization of the kinetic intermediate microtubule-GDP-Pi using phosphate analogues.微管蛋白聚合过程中GTP水解的机制:使用磷酸盐类似物对动力学中间体微管-GDP-磷酸进行表征。
Biochemistry. 1989 Feb 21;28(4):1783-91. doi: 10.1021/bi00430a054.
4
Interrelationships of tubulin-GDP and tubulin-GTP in microtubule assembly.微管组装中微管蛋白 - GDP与微管蛋白 - GTP的相互关系。
Biochemistry. 1987 Nov 3;26(22):7173-82. doi: 10.1021/bi00396a045.
5
Direct incorporation of guanosine 5'-diphosphate into microtubules without guanosine 5'-triphosphate hydrolysis.鸟苷5'-二磷酸直接掺入微管而无需鸟苷5'-三磷酸水解。
Biochemistry. 1986 Nov 4;25(22):7054-62. doi: 10.1021/bi00370a045.
6
An isoenergetic exchange mechanism which accounts for tubulin-GDP stabilization of microtubules.一种等能交换机制,该机制解释了微管蛋白-GDP对微管的稳定作用。
J Biol Chem. 1981 Dec 10;256(23):12051-7.
7
Inhibition of microtubule elongation by GDP.GDP对微管伸长的抑制作用。
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Dephosphorylation of tubulin-bound guanosine triphosphate during microtubule assembly.微管组装过程中与微管蛋白结合的鸟苷三磷酸的去磷酸化作用。
J Biochem. 1975 Jun;77(6):1193-7.
9
Incorporation of GDP-tubulin during elongation of microtubules in vitro.体外微管延长过程中GDP-微管蛋白的掺入。
Biochem Biophys Res Commun. 1985 Aug 30;131(1):386-94. doi: 10.1016/0006-291x(85)91814-5.
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Interactions of tubulin with guanine nucleotides that have paclitaxel-like effects on tubulin assembly: 2',3'-dideoxyguanosine 5'-[alpha,beta-methylene]triphosphate, guanosine 5'-[alpha,beta-methylene]triphosphate, and 2',3'-dideoxyguanosine 5'-triphosphate.对微管蛋白组装具有紫杉醇样作用的鸟嘌呤核苷酸与微管蛋白的相互作用:2',3'-二脱氧鸟苷5'-[α,β-亚甲基]三磷酸、鸟苷5'-[α,β-亚甲基]三磷酸和2',3'-二脱氧鸟苷5'-三磷酸。
Arch Biochem Biophys. 1995 Oct 1;322(2):486-99. doi: 10.1006/abbi.1995.1492.

引用本文的文献

1
Physical effects of crowdant size and concentration on collective microtubule polymerization.拥挤剂大小和浓度对微管集体聚合的物理影响。
Biophys J. 2025 Mar 4;124(5):789-806. doi: 10.1016/j.bpj.2025.01.020. Epub 2025 Jan 29.
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Clamped-filament elongation model for actin-based motors.基于肌动蛋白的马达的夹丝伸长模型。
Biophys J. 2002 Feb;82(2):605-17. doi: 10.1016/S0006-3495(02)75425-8.
3
Response of microtubules to the addition of colchicine and tubulin-colchicine: evaluation of models for the interaction of drugs with microtubules.微管对秋水仙碱和微管蛋白 - 秋水仙碱添加的反应:药物与微管相互作用模型的评估
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Role of GTP hydrolysis in microtubule treadmilling and assembly.GTP水解在微管踏车运动和组装中的作用。
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5
Nucleation and the kinetics of microtubule assembly.微管组装的成核作用与动力学
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7302-5. doi: 10.1073/pnas.77.12.7302.
6
Guanosine-5'-triphosphate hydrolysis and tubulin polymerization. Review article.鸟苷-5'-三磷酸水解与微管蛋白聚合。综述文章。
Mol Cell Biochem. 1982 Sep 3;47(2):97-113. doi: 10.1007/BF00234410.
7
Cytoplasmic microtubule assembly-disassembly from endogenous tubulin in a Brij-lysed cell model.在Brij裂解细胞模型中,细胞质微管由内源性微管蛋白进行组装和解聚。
J Cell Biol. 1983 Jun;96(6):1631-41. doi: 10.1083/jcb.96.6.1631.
8
Activation and attenuation of adenylate cyclase. The role of GTP-binding proteins as macromolecular messengers in receptor--cyclase coupling.腺苷酸环化酶的激活与衰减。GTP结合蛋白作为受体 - 环化酶偶联中大分子信使的作用。
Biochem J. 1981 Apr 1;195(1):1-13. doi: 10.1042/bj1950001.
9
Dynamic instability of individual microtubules analyzed by video light microscopy: rate constants and transition frequencies.通过视频光学显微镜分析单个微管的动态不稳定性:速率常数和转变频率。
J Cell Biol. 1988 Oct;107(4):1437-48. doi: 10.1083/jcb.107.4.1437.

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Turbidimetric studies of the in vitro assembly and disassembly of porcine neurotubules.猪神经微管体外组装与拆卸的比浊法研究。
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Microtubular protein reaction with nucleotides.微管蛋白与核苷酸的反应。
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J Biochem. 1975 Jun;77(6):1193-7.
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The role of the bound nucleotide in the polymerization of actin.结合核苷酸在肌动蛋白聚合中的作用。
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Role of nucleotide hydrolysis in microtubule assembly.核苷酸水解在微管组装中的作用。
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Tubulin-nucleotide interactions during the polymerization and depolymerization of microtubules.微管聚合和解聚过程中的微管蛋白-核苷酸相互作用。
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Role of GTP in the assembly of microtubules.鸟苷三磷酸在微管组装中的作用。
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Microtubular protein catalytic interactions with nucleotides.微管蛋白与核苷酸的催化相互作用。
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Properties of tubulin treated with alkaline phosphatase to remove guanine nucleotides from the exchangeable binding site.
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鸟嘌呤核苷酸在微管组装的成核和延伸步骤中的参与。

Participation of guanine nucleotides in nucleation and elongation steps of microtubule assembly.

作者信息

Karr T L, Podrasky A E, Purich D L

出版信息

Proc Natl Acad Sci U S A. 1979 Nov;76(11):5475-9. doi: 10.1073/pnas.76.11.5475.

DOI:10.1073/pnas.76.11.5475
PMID:293656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC411671/
Abstract

Critical concentrations for formation of microtubules from subunits with GTP and its beta, gamma-imido and beta, gamma-methylene analogs are similar when adequate time is given for equilibration. Dilution of microtubules into GTP and GDP yielded values of 0.1 and 0.19 mg/ml for the critical concentration, results similar to those reported by Carlier and Pantaloni [Carlier, M. & Pantaloni, D. (1978) Biochemistry 17, 1908-1915]. GDP is capable of supporting elongation of preformed microtubules, but it efficiently poisons the nucleation events. Reported experiments also demonstrate that the critical tubulin concentration of the tubulin-GDP complex can be accurately measured in both the assembly and disassembly directions. Evidence is presented that GTP is involved in early nucleation events but that microtubules are stabilized in the presence of either GTP or GDP. These results are discussed in terms of a condensation-equilibrium model in which tubulin subunits equilibrate rapidly with microtubule ends, and their affinity for the ends is governed by the nucleotide ligand at the exchangeable site.

摘要

如果给予足够时间进行平衡,由带有鸟苷三磷酸(GTP)及其β,γ-亚氨基和β,γ-亚甲基类似物的亚基形成微管的临界浓度是相似的。将微管稀释到GTP和鸟苷二磷酸(GDP)中,得到的临界浓度值分别为0.1和0.19毫克/毫升,这一结果与卡利尔(Carlier)和潘塔洛尼(Pantaloni)报道的结果相似[卡利尔,M. & 潘塔洛尼,D.(1978年)《生物化学》17卷,1908 - 1915页]。GDP能够支持预先形成的微管的延长,但它会有效地抑制成核事件。已报道的实验还表明,在组装和解聚方向上都可以准确测量微管蛋白 - GDP复合物的临界微管蛋白浓度。有证据表明,GTP参与早期成核事件,但微管在GTP或GDP存在的情况下都会稳定下来。这些结果将根据一个凝聚 - 平衡模型进行讨论,在该模型中,微管蛋白亚基与微管末端快速平衡,并且它们对末端的亲和力由可交换位点处的核苷酸配体决定。