Cryo-Electron Tomography and Proteomics studies of centrosomes from differentiated quiescent thymocytes.
Johan BusselezFrancisco Javier ChichónMaria Josefa RodríguezAdan AlpízarSéverine Isabelle GharbiMònica FranchRoberto MeleroAlberto ParadelaJosé L CarrascosaJosé María CarazoPublished in: Scientific reports (2019)
We have used cryo Electron Tomography, proteomics and immunolabeling to study centrosomes isolated from the young lamb thymus, an efficient source of quiescent differentiated cells. We compared the proteome of thymocyte centrosomes to data published for KE37 cells, focusing on proteins associated with centriole disengagement and centrosome separation. The data obtained enhances our understanding of the protein system joining the centrioles, a system comprised of a branched network of fibers linked to an apparently amorphous density that was partially characterized here. A number of proteins were localized to the amorphous density by immunolabeling (C-NAP1, cohesin SMC1, condensin SMC4 and NCAPD2), yet not DNA. In conjuction, these data not only extend our understanding of centrosomes but they will help refine the model that focus on the protein system associated with the centriolar junction.
Keyphrases
- electron microscopy
- induced apoptosis
- electronic health record
- cell cycle arrest
- big data
- mass spectrometry
- high resolution
- endoplasmic reticulum stress
- room temperature
- machine learning
- amino acid
- cell death
- systematic review
- oxidative stress
- signaling pathway
- single molecule
- label free
- pi k akt
- middle aged
- ionic liquid
- cell proliferation
- solar cells
- artificial intelligence