What organizes the molecular ballet that promotes the movement of the axoneme in such a way that its molecular machinery seems to be a whole?

AIP Conference Proceedings

Volumn 755, Issue , 2005, Pages 117-129

  Cibert, Christian ^a  

^a Groupe de Morphométrie et de Modélisation Cellulaire   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33748535140     PISSN: 0094243X     EISSN: 15517616     Source Type: Conference Proceeding    
DOI: 10.1063/1.1900398     Document Type: Conference Paper

References (20)

1. Burgess, S. and P. Knight, Is the dynein motor a winch? Curr. Opin. Struct. Biol., 2004, 14: p. 138-46.
2. Burgess, S., et al., Dynein struture and power stroke. Nature, 2003. 421: p. 715-8.
3. Cibert, C., Elastic extension and jump of the flagellar nexin links: a theoretical mechanical cycle. Cell Motil. Cytoskel., 2001. 49: p. 161-75.
4. Gibbons, I., Cilia and flagella of eukaryotes. J. Cell Biol., 1981. 91(3): p. 107s-24s.
5. Brokaw, C.J., Direct measurements of sliding between outer doublet microtubules in swimming sperm flagella. Science, 1989. 243: p. 1593-1596.
6. Brokaw, C., Microtubule sliding, bend formation, and bend propagation parameters of Ciona sperm flagella altered by viscous load. Cell Motil. Cystoskel, 1996. 33: p. 6-21.
7. Ricard, J., What do we mean by biological complexity? C R Biol, 2003. 326(2): p. 133-40.
8. Cibert, C., A cascade of biochemical events creates emergence. Biol Cell, 2004. 96(9): p. 677-9.
9. Srere, P.A., The metabolon. Trends Biochem Sci, 1985. 10: p. 109-10.
10. Goldbeter, A. and G. Dupont, Allosteric regulation, cooperatively, and biochemical oscillations. Biophys. Chem., 1990. 37: p. 341-53.
11. Cibert, C., Axonemal activity relative to the 2D/3D-waveform conversion of the flagellum. Cell Motility and the Cytoskeleton, 2002. 51: p. 89-111.
12. Cibert, C., Entropy and information in flagellar axoneme cybernetics: a radial spokes integrative function. Cell motility and the Cytoskeleton, 2003. 54: p. 296-316.
13. Mitchell, D.R. and M. Nakatsugawa, Bend propagation drives central pair rotation in Chlamydomonas reinhardtii flagella. J Cell Biol, 2004. 166(5): p. 709-15.
14. Warner, F., Cross-bridge mechanism in ciliary motility: the sliding-bending conversion, in Cell Motility (Part C), R. Goldman, T. Pollard, and J. Rosenbaum, Editors. 1976, Cold Spring Harbor Laboratory, p. 891-914.
15. Cibert, C. and J.-V. Heck, Geometry drives the "deviated- bending" of the bitubular structures of the 9+2 axoneme in the flagellum. Cell Motility and the Cytoskeleton, 2004. 59: p. 153-68.
16. Kasas, S., et al., Mechanical properties of microtubules explored using the finite elements method. Chemphyschem., 2004. 5: p. 252-7.
17. Kasas, S., et al., Oscillation modes of microtubules. Biol Cell, 2004. 96(9): p. 697-700.
18. Kis, A., et al., Nanomechanics of microtubules. Physical review letters, 2002. 89(24): p. 1-4.
19. Ricard, J., Reduction, integration and emergence in biochemical networks. Biol Cell, 2004. 96(9): p. 719-25.
20. Inaba, K., Molecular architecture of the sperm flagella: molecules for motility and signaling. Zoolog. Sci., 2003. 20: p. 1043-56.