Kinesin is an evolutionarily fine-tuned molecular ratchet-and-pawl device of decisively locked direction

Zhisong Wang, Min Feng, Wenwei Zheng, Dagong Fan

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

Abstract

Conventional kinesin is a dimeric motor protein that transports membranous organelles toward the plus-end of microtubules (MTs). Individual kinesin dimers show steadfast directionality and hundreds of consecutive steps, yet the detailed physical mechanism remains unclear. Here we compute free energies for the entire dimer-MT system for all possible interacting configurations by taking full account of molecular details. Employing merely first principles and several measured binding and barrier energies, the system-level analysis reveals insurmountable energy gaps between configurations, asymmetric ground state caused by mechanically lifted configurational degeneracy, and forbidden transitions ensuring coordination between both motor domains for alternating catalysis. This wealth of physical effects converts a kinesin dimer into a molecular ratchet-and-pawl device, which determinedly locks the dimer's movement into the MT plus-end and ensures consecutive steps in hand-over-hand gait. Under a certain range of extreme loads, however, the ratchet-and-pawl device becomes defective but not entirely abolished to allow consecutive back-steps. This study yielded quantitative evidence that kinesin's multiple molecular properties have been evolutionarily adapted to fine-tune the ratchet-and-pawl device so as to ensure the motor's distinguished performance.

Original languageEnglish (US)
Pages (from-to)3363-3372
Number of pages10
JournalBiophysical journal
Volume93
Issue number10
DOIs
StatePublished - Nov 2007
Externally publishedYes

ASJC Scopus subject areas

  • Biophysics

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