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dc.contributor.authorEngel, Benjamin D.
dc.contributor.authorLechtreck, Karl-Ferdinand
dc.contributor.authorSakai, Tsuyoshi
dc.contributor.authorIkebe, Mitsuo
dc.contributor.authorWitman, George B.
dc.contributor.authorMarshall, Wallace F.
dc.date2022-08-11T08:11:05.000
dc.date.accessioned2022-08-23T17:33:04Z
dc.date.available2022-08-23T17:33:04Z
dc.date.issued2009-01-01
dc.date.submitted2011-01-21
dc.identifier.citationMethods Cell Biol. 2009;93:157-77. Epub 2009 Dec 4. <a href="http://dx.doi.org/10.1016/S0091-679X(08)93009-0">Link to article on publisher's site</a>
dc.identifier.issn0091-679X (Linking)
dc.identifier.doi10.1016/S0091-679X(08)93009-0
dc.identifier.urihttp://hdl.handle.net/20.500.14038/51090
dc.description.abstractThe eukaryotic flagellum is host to a variety of dynamic behaviors, including flagellar beating, the motility of glycoproteins in the flagellar membrane, and intraflagellar transport (IFT), the bidirectional traffic of protein particles between the flagellar base and tip. IFT is of particular interest, as it plays integral roles in flagellar length control, cell signaling, development, and human disease. However, our ability to understand dynamic flagellar processes such as IFT is limited in large part by the fidelity with which we can image these behaviors in living cells. This chapter introduces the application of total internal reflection fluorescence (TIRF) microscopy to visualize the flagella of Chlamydomonas reinhardtii. The advantages and challenges of TIRF are discussed in comparison to confocal and differential interference contrast techniques. This chapter also reviews current IFT insights gleaned from TIRF microscopy of Chlamydomonas and provides an outlook on the future of the technique, with particular emphasis on combining TIRF with other emerging imaging technologies.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20409817&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/S0091-679X(08)93009-0
dc.subjectAnimals
dc.subjectAxoneme
dc.subjectBiological Transport
dc.subjectChlamydomonas reinhardtii
dc.subjectFlagella
dc.subjectFluorescence Recovery After Photobleaching
dc.subjectGreen Fluorescent Proteins
dc.subjectHumans
dc.subjectMicroscopy, Fluorescence
dc.subjectMolecular Motor Proteins
dc.subjectProtozoan Proteins
dc.subjectRecombinant Fusion Proteins
dc.subjectCell Biology
dc.titleTotal internal reflection fluorescence (TIRF) microscopy of Chlamydomonas flagella
dc.typeJournal Article
dc.source.journaltitleMethods in cell biology
dc.source.volume93
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/witman/5
dc.identifier.contextkey1739063
html.description.abstract<p>The eukaryotic flagellum is host to a variety of dynamic behaviors, including flagellar beating, the motility of glycoproteins in the flagellar membrane, and intraflagellar transport (IFT), the bidirectional traffic of protein particles between the flagellar base and tip. IFT is of particular interest, as it plays integral roles in flagellar length control, cell signaling, development, and human disease. However, our ability to understand dynamic flagellar processes such as IFT is limited in large part by the fidelity with which we can image these behaviors in living cells. This chapter introduces the application of total internal reflection fluorescence (TIRF) microscopy to visualize the flagella of Chlamydomonas reinhardtii. The advantages and challenges of TIRF are discussed in comparison to confocal and differential interference contrast techniques. This chapter also reviews current IFT insights gleaned from TIRF microscopy of Chlamydomonas and provides an outlook on the future of the technique, with particular emphasis on combining TIRF with other emerging imaging technologies.</p>
dc.identifier.submissionpathwitman/5
dc.contributor.departmentDepartment of Physiology
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages157-77


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