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STED nanoscopy of the centrosome linker reveals a CEP68-organized, periodic rootletin network anchored to a C-Nap1 ring at centrioles
Rifka Vlijm, Xue Li, Marko Panic, Diana Rüthnick, Shoji Hata, Frank Herrmannsdörfer, Thomas Kuner, Mike Heilemann, Johann Engelhardt, Stefan W. Hell, and Elmar Schiebel
PNAS February 20, 2018. 201716840; published ahead of print February 20, 2018. https://doi.org/10.1073/pnas.1716840115
Rifka Vlijm
aDepartment of Optical Nanoscopy, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany;bDepartment of Optical Nanoscopy, Max Planck Institute for Medical Research, 69120 Heidelberg, Germany;
Xue Li
cZentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Universität Heidelberg, 69120 Heidelberg, Germany;dHartmut Hoffmann-Berling International Graduate School of Molecular and Cellular Biology, Universität Heidelberg, 69120 Heidelberg, Germany;
Marko Panic
cZentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Universität Heidelberg, 69120 Heidelberg, Germany;dHartmut Hoffmann-Berling International Graduate School of Molecular and Cellular Biology, Universität Heidelberg, 69120 Heidelberg, Germany;
Diana Rüthnick
cZentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Universität Heidelberg, 69120 Heidelberg, Germany;
Shoji Hata
cZentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Universität Heidelberg, 69120 Heidelberg, Germany;
Frank Herrmannsdörfer
eDepartment of Functional Neuroanatomy, Institute for Anatomy and Cell Biology, Universität Heidelberg, 69120 Heidelberg, Germany;
Thomas Kuner
eDepartment of Functional Neuroanatomy, Institute for Anatomy and Cell Biology, Universität Heidelberg, 69120 Heidelberg, Germany;
Mike Heilemann
eDepartment of Functional Neuroanatomy, Institute for Anatomy and Cell Biology, Universität Heidelberg, 69120 Heidelberg, Germany;fBioQuant, Universität Heidelberg, 69120 Heidelberg, Germany;gInstitute of Physical and Theoretical Chemistry, Johann Wolfgang Goethe-University, 60438 Frankfurt, Germany;
Johann Engelhardt
aDepartment of Optical Nanoscopy, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany;bDepartment of Optical Nanoscopy, Max Planck Institute for Medical Research, 69120 Heidelberg, Germany;
Stefan W. Hell
aDepartment of Optical Nanoscopy, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany;bDepartment of Optical Nanoscopy, Max Planck Institute for Medical Research, 69120 Heidelberg, Germany;hDepartment of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany
Elmar Schiebel
cZentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Universität Heidelberg, 69120 Heidelberg, Germany;
Supporting Information
- Download Supporting Information (PDF)
- Download Appendix (PDF)
- Download Dataset_S01 (PDF)
- Download Movie_S01 (AVI) - Centrosome movement in RPE1 cells. The two centrosomes of an interphase cell are kept together in a dynamic way (representative for ∼95% of the cells). mNeonGreen-CEP68 is shown in green; mRuby2-PACT is shown in red and serves as centrosome marker.
- Download Movie_S02 (AVI) - Centrosome movement in RPE1 cells, similar to Movie S1. The two centrosomes of an interphase cell are kept together in a dynamic way (representative for ∼95% of the cells). mNeonGreen-CEP68 is shown in green; mRuby2-PACT is shown in red and serves as centrosome marker.
- Download Movie_S03 (AVI) - Centrosome movement in RPE1 cells, similar to Movies S1 and S2. The two centrosomes of an interphase cell are kept together in a dynamic way (representative for ∼95% of the cells). mNeonGreen-CEP68 is shown in green; mRuby2-PACT is shown in red and serves as centrosome marker.
- Download Movie_S04 (AVI) - Centrosome movement in RPE1 cells. The separated centrosomes of a cell in interphase are joined and stay together thereafter (representative for ∼5% of the cells). mNeonGreen-CEP68 is shown in green; mRuby2-PACT is shown in red and serves as centrosome marker.
- Download Movie_S05 (AVI) - Centrosome movement in RPE1 cells, similar to Movie S4. The separated centrosomes of a cell in interphase are joined and stay together thereafter (representative for ∼5% of the cells). mNeonGreen-CEP68 is in green; mRuby2-PACT is shown in red and serves as centrosome marker.
- Download Movie_S06 (AVI) - Centrosome movement in RPE1 cells, similar to Movies S4 and S5. The separated centrosomes of a cell in interphase are joined and stay together thereafter (representative for ∼5% of the cells). mNeonGreen-CEP68 is shown in green; mRuby2-PACT is shown in red and serves as centrosome marker.
- Download Movie_S07 (AVI) - A 3D image of a rootletin fiber network imaged by 3D-STORM.
- Download Movie_S08 (AVI) - A 3D image of a single rootletin fiber imaged by 3D-STORM.
- Download Movie_S09 (AVI) - A 3D image of a CEP68 fiber network imaged by 3D-STORM.