TY - JOUR
T1 - Structural heterogeneity of cellular k5/k14 filaments as revealed by cryo-electron microscopy
AU - Weber, Miriam S.
AU - Eibauer, Matthias
AU - Sivagurunathan, Suganya
AU - Magin, Thomas M.
AU - Goldman, Robert D.
AU - Medalia, Ohad
N1 - Funding Information:
laboratory is supported by grants 5PO1 GM096971 and RO1GM140108 from the National Institutes
Funding Information:
This research was funded by the Swiss National Science Foundation Grant (31003A_179418). M.S.W. was supported by the Forschungskredit of the University of Zurich (FK-18-041). The Goldman laboratory is supported by grants 5PO1 GM096971 and RO1GM140108 from the National Institutes of Health.
Funding Information:
was supported by the Forschungskredit of the University of Zurich (FK-18-041). The Goldman
Funding Information:
This research was funded by the Swiss National Science Foundation Grant (31003A_179418). M.S.W.
Publisher Copyright:
© 2021, eLife Sciences Publications Ltd. All rights reserved.
PY - 2021/7
Y1 - 2021/7
N2 - Keratin intermediate filaments are an essential and major component of the cytoskeleton in epithelial cells. They form a stable yet dynamic filamentous network extending from the nucleus to the cell periphery, which provides resistance to mechanical stresses. Mutations in keratin genes are related to a variety of epithelial tissue diseases. Despite their importance, the molecular structure of keratin filaments remains largely unknown. In this study, we analyzed the structure of keratin 5/keratin 14 filaments within ghost mouse keratinocytes by cryo-electron microscopy and cryo-electron tomography. By averaging a large number of keratin segments, we have gained insights into the helical architecture of the filaments. Two-dimensional classification revealed profound variations in the diameter of keratin filaments and their subunit organization. Computational reconstitution of filaments of substantial length uncovered a high degree of internal heterogeneity along single filaments, which can contain regions of helical symmetry, regions with less symmetry and regions with significant diameter fluctuations. Cross section views of filaments revealed that keratins form hollow cylinders consisting of multiple protofilaments, with an electron dense core located in the center of the filament. These findings shed light on the complex and remarkable heterogenic architecture of keratin filaments, suggesting that they are highly flexible, dynamic cytoskeletal structures.
AB - Keratin intermediate filaments are an essential and major component of the cytoskeleton in epithelial cells. They form a stable yet dynamic filamentous network extending from the nucleus to the cell periphery, which provides resistance to mechanical stresses. Mutations in keratin genes are related to a variety of epithelial tissue diseases. Despite their importance, the molecular structure of keratin filaments remains largely unknown. In this study, we analyzed the structure of keratin 5/keratin 14 filaments within ghost mouse keratinocytes by cryo-electron microscopy and cryo-electron tomography. By averaging a large number of keratin segments, we have gained insights into the helical architecture of the filaments. Two-dimensional classification revealed profound variations in the diameter of keratin filaments and their subunit organization. Computational reconstitution of filaments of substantial length uncovered a high degree of internal heterogeneity along single filaments, which can contain regions of helical symmetry, regions with less symmetry and regions with significant diameter fluctuations. Cross section views of filaments revealed that keratins form hollow cylinders consisting of multiple protofilaments, with an electron dense core located in the center of the filament. These findings shed light on the complex and remarkable heterogenic architecture of keratin filaments, suggesting that they are highly flexible, dynamic cytoskeletal structures.
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U2 - 10.5061/dryad.gqnk98sn4
DO - 10.5061/dryad.gqnk98sn4
M3 - Article
C2 - 34323216
AN - SCOPUS:85111435417
SN - 2050-084X
VL - 10
JO - eLife
JF - eLife
ER -