English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Selective chemical crosslinking reveals a Cep57-Cep63-Cep152 centrosomal complex.

MPS-Authors
/persons/resource/persons203920

Lukinavicius,  G.
Laboratory of Chromatin Labeling and Imaging, Max Planck Institute for Biophysical Chemistry, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

2627955.pdf
(Publisher version), 853KB

Supplementary Material (public)

2627955_Suppl.pdf
(Supplementary material), 2MB

Citation

Lukinavicius, G., Lavogina, D., Orpinell, M., Umezawa, K., Reymond, L., Garin, N., et al. (2013). Selective chemical crosslinking reveals a Cep57-Cep63-Cep152 centrosomal complex. Current Biology, 23(4), 265-270. doi:10.1016/j.cub.2012.12.030.


Cite as: https://hdl.handle.net/21.11116/0000-0001-DAEA-2
Abstract
The centrosome functions as the main microtubule-organizing center of animal cells and is crucial for several fundamental cellular processes. Abnormalities in centrosome number and composition correlate with tumor progression and other diseases. Although proteomic studies have identified many centrosomal proteins, their interactions are incompletely characterized. The lack of information on the precise localization and interaction partners for many centrosomal proteins precludes comprehensive understanding of centrosome biology. Here, we utilize a combination of selective chemical crosslinking and superresolution microscopy to reveal novel functional interactions among a set of 31 centrosomal proteins. We reveal that Cep57, Cep63, and Cep152 are parts of a ring-like complex localizing around the proximal end of centrioles. Furthermore, we identify that STIL, together with HsSAS-6, resides at the proximal end of the procentriole, where the cartwheel is located. Our studies also reveal that the known interactors Cep152 and Plk4 reside in two separable structures, suggesting that the kinase Plk4 contacts its substrate Cep152 only transiently, at the centrosome or within the cytoplasm. Our findings provide novel insights into protein interactions critical for centrosome biology and establish a toolbox for future studies of centrosomal proteins.