Fluorescence Imaging of Single Kinesin Motors on Immobilized Microtubules

Research output: Contribution to book/conference proceedings/anthology/reportChapter in book/anthology/reportContributedpeer-review

Contributors

  • Till Korten - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Bert Nitzsche - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Chris Gell - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Felix Ruhnow - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Cécile Leduc - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Stefan Diez - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)

Abstract

Recent developments in optical microscopy and nanometer tracking have greatly improved our understanding of cytoskeletal motor proteins. Using fluorescence microscopy, dynamic interactions are now routinely observed in vitro on the level of single molecules mainly using a geometry, where fluorescently labeled motors move on surface-immobilized filaments. In this chapter, we review recent methods related to single-molecule kinesin motility assays. In particular, we aim to provide practical advice on: how to set up the assays, how to acquire high-precision data from fluorescently labeled kinesin motors and attached quantum dots, and how to analyze data by nanometer tracking.

Details

Original languageEnglish
Title of host publicationSingle Molecule Analysis
PublisherHumana Press
Pages121-137
Number of pages17
ISBN (print)9781617792816
Publication statusPublished - 2011
Peer-reviewedYes
Externally publishedYes

Publication series

SeriesMethods in Molecular Biology
Volume783
ISSN1064-3745

External IDs

PubMed 21909886
ORCID /0000-0002-0750-8515/work/161407040

Keywords

ASJC Scopus subject areas

Keywords

  • Imaging, Kinesin, Microtubule, Motor protein, Single molecule, TIRF microscopy