Quantitative analysis of human centrosome architecture by targeted proteomics and fluorescence imaging

التفاصيل البيبلوغرافية
العنوان: Quantitative analysis of human centrosome architecture by targeted proteomics and fluorescence imaging
المؤلفون: Manuel Bauer, Erich A. Nigg, Fabien Cubizolles, Alexander Schmidt
المصدر: The EMBO journal
The EMBO Journal
سنة النشر: 2016
مصطلحات موضوعية: Proteomics, Resource, 0301 basic medicine, PLK4, Centriole, Cell Cycle Proteins, Centrosome cycle, Biology, Ciliopathies, General Biochemistry, Genetics and Molecular Biology, Cell Line, 03 medical and health sciences, fluorescence imaging, Humans, centriole, Molecular Biology, Centrosome, General Immunology and Microbiology, General Neuroscience, Cilium, Optical Imaging, Cell Cycle, Post-translational Modifications, Proteolysis & Proteomics, Epithelial Cells, Cell biology, 030104 developmental biology, selected reaction monitoring, Cell Adhesion, Polarity & Cytoskeleton, Function (biology), Biogenesis
الوصف: Centrioles are essential for the formation of centrosomes and cilia. While numerical and/or structural centrosomes aberrations are implicated in cancer, mutations in centriolar and centrosomal proteins are genetically linked to ciliopathies, microcephaly, and dwarfism. The evolutionarily conserved mechanisms underlying centrosome biogenesis are centered on a set of key proteins, including Plk4, Sas‐6, and STIL, whose exact levels are critical to ensure accurate reproduction of centrioles during cell cycle progression. However, neither the intracellular levels of centrosomal proteins nor their stoichiometry within centrosomes is presently known. Here, we have used two complementary approaches, targeted proteomics and EGFP‐tagging of centrosomal proteins at endogenous loci, to measure protein abundance in cultured human cells and purified centrosomes. Our results provide a first assessment of the absolute and relative amounts of major components of the human centrosome. Specifically, they predict that human centriolar cartwheels comprise up to 16 stacked hubs and 1 molecule of STIL for every dimer of Sas‐6. This type of quantitative information will help guide future studies of the molecular basis of centrosome assembly and function.
DOI: 10.15252/embj.201694462
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b9b9ddabc5fd230640d181138a7288Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....26b9b9ddabc5fd230640d181138a7288
قاعدة البيانات: OpenAIRE