Show simple item record

dc.contributor.authorGui, Miao
dc.contributor.authorMa, Meisheng
dc.contributor.authorSze-Tu, Erica
dc.contributor.authorWang, Xiangli
dc.contributor.authorKoh, Fujiet
dc.contributor.authorZhong, Ellen D
dc.contributor.authorBerger, Bonnie
dc.contributor.authorDavis, Joseph H
dc.contributor.authorDutcher, Susan K
dc.contributor.authorZhang, Rui
dc.contributor.authorBrown, Alan
dc.date.accessioned2021-10-27T19:52:37Z
dc.date.available2021-10-27T19:52:37Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/133399
dc.description.abstract© 2020, The Author(s), under exclusive licence to Springer Nature America, Inc. In motile cilia, a mechanoregulatory network is responsible for converting the action of thousands of dynein motors bound to doublet microtubules into a single propulsive waveform. Here, we use two complementary cryo-EM strategies to determine structures of the major mechanoregulators that bind ciliary doublet microtubules in Chlamydomonas reinhardtii. We determine structures of isolated radial spoke RS1 and the microtubule-bound RS1, RS2 and the nexin−dynein regulatory complex (N-DRC). From these structures, we identify and build atomic models for 30 proteins, including 23 radial-spoke subunits. We reveal how mechanoregulatory complexes dock to doublet microtubules with regular 96-nm periodicity and communicate with one another. Additionally, we observe a direct and dynamically coupled association between RS2 and the dynein motor inner dynein arm subform c (IDAc), providing a molecular basis for the control of motor activity by mechanical signals. These structures advance our understanding of the role of mechanoregulation in defining the ciliary waveform.
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.relation.isversionof10.1038/s41594-020-00530-0
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.sourcePMC
dc.titleStructures of radial spokes and associated complexes important for ciliary motility
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Program
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mathematics
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.relation.journalNature Structural and Molecular Biology
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-07-15T18:08:08Z
dspace.orderedauthorsGui, M; Ma, M; Sze-Tu, E; Wang, X; Koh, F; Zhong, ED; Berger, B; Davis, JH; Dutcher, SK; Zhang, R; Brown, A
dspace.date.submission2021-07-15T18:08:10Z
mit.journal.volume28
mit.journal.issue1
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record