Mechanochemical model of microtubule structure and self-assembly kinetics

被引:194
|
作者
VanBuren, V
Cassimeris, L
Odde, DJ
机构
[1] Lehigh Univ, Dept Biol Sci, Bethlehem, PA 18015 USA
[2] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN USA
关键词
D O I
10.1529/biophysj.105.060913
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Microtubule self-assembly is largely governed by the chemical kinetics and thermodynamics of tubulin-tubulin interactions. An important aspect of microtubule assembly is that hydrolysis of the beta-tubulin-associated GTP promotes proto. lament curling. Proto. lament curling presumably drives the transition from tip structures associated with growth (sheetlike projections and blunt ends) to those associated with shortening (rams' horns and frayed ends), and transitions between these structures have been proposed to be important for growth-shortening transitions. However, previous models for microtubule dynamic instability have not considered such structures or mechanics explicitly. Here we present a three-dimensional model that explicitly incorporates mechanical stress and strain within the microtubule lattice. First, we found that the model recapitulates three-dimensional tip structures and rates of assembly and disassembly for microtubules grown under standard conditions, and we propose that taxol may stabilize microtubule growth by reducing flexural rigidity. Second, in contrast to recent suggestions, it was determined that sheetlike tips are more likely to undergo catastrophe than blunt tips. Third, partial uncapping of the tubulin-GTP cap provides a possible mechanism for microtubule pause events. Finally, simulations of the binding and structural effects of XMAP215 produced the experimentally observed growth and shortening rates, and tip structure.
引用
收藏
页码:2911 / 2926
页数:16
相关论文
共 50 条
  • [31] KINETICS OF STREPTOLYSIN-O SELF-ASSEMBLY
    PALMER, M
    VALEVA, A
    KEHOE, M
    BHAKDI, S
    EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 231 (02): : 388 - 395
  • [32] Mechanochemical Preparation and Self-Assembly of Protein:Dye Hybrids for White Luminescence
    Yuan, Yusheng
    Solin, Niclas
    ACS APPLIED POLYMER MATERIALS, 2021, 3 (10) : 4825 - 4836
  • [33] Kinetics of intermediate-mediated self-assembly in nanosized materials: A generic model
    Lutsko, James F.
    Basios, Vasileios
    Nicolis, Gregoire
    Caremans, Tom P.
    Aerts, Alexander
    Martens, Johan A.
    Kirschhock, Christine E. A.
    van Erp, Titus S.
    JOURNAL OF CHEMICAL PHYSICS, 2010, 132 (16):
  • [34] Revealing Thermodynamics and Kinetics of Lipid Self-Assembly by Markov State Model Analysis
    Weng, Jingwei
    Yang, Maohua
    Wang, Wenning
    Xu, Xin
    Tian, Zhongqun
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (51) : 21344 - 21352
  • [35] Structure Formation by Dynamic Self-Assembly
    Li, Liqiang
    Koepf, Michael H.
    Gurevich, Svetlana V.
    Friedrich, Rudolf
    Chi, Lifeng
    SMALL, 2012, 8 (04) : 488 - 503
  • [36] GLYCOLIPID SELF-ASSEMBLY - MICELLAR STRUCTURE
    CECUTTI, C
    FOCHER, B
    PERLY, B
    ZEMB, T
    LANGMUIR, 1991, 7 (11) : 2580 - 2585
  • [37] The self-assembly and structure of caseins in solution
    Morris, GA
    BIOTECHNOLOGY & GENETIC ENGINEERING REVIEWS, VOL 19, 2002, 19 : 357 - 376
  • [38] DNA ionogel: Structure and self-assembly
    Pandey, Pankaj Kumar
    Rawat, Kamla
    Aswal, V. K.
    Kohlbrechere, J.
    Bohidar, H. B.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2017, 19 (01) : 804 - 812
  • [39] The self-assembly and structure of caseins in solution
    Morris, Gordon A.
    Biotechnology and Genetic Engineering Reviews, 2002, 19 : 357 - 376
  • [40] Macromolecular structure and self-assembly - Discussion
    Rose
    Henderson
    Garcia-Bellido
    Holmes
    Hess
    Perutz
    Raff
    Noble
    Dover
    LIMITS OF REDUCTIONISM IN BIOLOGY, 1998, 213 : 52 - 55