Protein interactors of Spindle Pole Body (SPB) components and septal proteins in fungus : A mass spectrometry-based dataset.

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Departamento de Microbiología. Centro de Investigación Científica y de Educación Superior de Ensenada (CICESE). Ensenada, B.C., Mexico.

Published: February 2024

AI Article Synopsis

  • Microtubule Organizing Centers (MTOC) are essential structures in eukaryotic cells for microtubule nucleation, differing in location based on species and cell type.
  • The Spindle Pole Body (SPB) functions as the main MTOC in fungi, while other variants, such as the Spitzenkörper, exist but aren't present in all species.
  • This study utilized mass spectrometry to analyze proteins interacting with various MTOC components tagged with fluorescent proteins, using a method called Co-IP to capture and identify these proteins.

Article Abstract

Microtubule Organizing Centers (MTOC) are subcellular structures in eukaryotic cells where nucleation of microtubules (MTs) takes place and represents the filament's minus end. Their localization depends on the species, cell type, and cell cycle stage. Along the fungal kingdom, the Spindle Pole Body (SPB) in the nucleus (an equivalent to Centrosomes in animal cells) is the principal MTOC. Other MTOCs have been identified in filamentous fungi, such as the Spitzenkörper in the hyphal tips of or the septal pore of . However, in the fungal-model organism , these alternative MTOCs have not been recognized. Here, we present a Mass spectrometry-based dataset of proteins interacting with four MTOC components of  tagged with fluorescent proteins: γ-Tubulin-sGFP (main nucleator at the SPB), MZT-1-sGFP (structural SPB microprotein), APS-2-dRFP (septal protein and recognized SPB component), and SPA-10-sGFP (septal MTOC protein). A WT and a cytosolic GFP expressing strain were included as controls. The protein interactors were pulled down by Co-IP, using GFP-Magnetic agarose that captures recombinant GFP proteins (including GFP-derivatives) in their native state. Bounded proteins were separated by SDS-PAGE and identified by nano LC-MS/MS. The protein annotation was done using the protein database.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10823093PMC
http://dx.doi.org/10.1016/j.dib.2023.109980DOI Listing

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