| Literature DB >> 28828861 |
Tiziana Alberio1, Luisa Pieroni2, Maurizio Ronci2,3, Cristina Banfi4, Italia Bongarzone5, Patrizia Bottoni6, Maura Brioschi4, Marianna Caterino7,8, Clizia Chinello9, Antonella Cormio10, Flora Cozzolino8,11, Vincenzo Cunsolo12, Simona Fontana13, Barbara Garavaglia14, Laura Giusti15, Viviana Greco2, Antonio Lucacchini15, Elisa Maffioli16, Fulvio Magni9, Francesca Monteleone13, Maria Monti8,11, Valentina Monti14, Clara Musicco17, Giuseppe Petrosillo17, Vito Porcelli10, Rosaria Saletti12, Roberto Scatena6, Alessio Soggiu16, Gabriella Tedeschi16,18, Mara Zilocchi1, Paola Roncada19, Andrea Urbani2,6, Mauro Fasano1.
Abstract
The Mitochondrial Human Proteome Project aims at understanding the function of the mitochondrial proteome and its crosstalk with the proteome of other organelles. Being able to choose a suitable and validated enrichment protocol of functional mitochondria, based on the specific needs of the downstream proteomics analysis, would greatly help the researchers in the field. Mitochondrial fractions from ten model cell lines were prepared using three enrichment protocols and analyzed on seven different LC-MS/MS platforms. All data were processed using neXtProt as reference database. The data are available for the Human Proteome Project purposes through the ProteomeXchange Consortium with the identifier PXD007053. The processed data sets were analyzed using a suite of R routines to perform a statistical analysis and to retrieve subcellular and submitochondrial localizations. Although the overall number of identified total and mitochondrial proteins was not significantly dependent on the enrichment protocol, specific line to line differences were observed. Moreover, the protein lists were mapped to a network representing the functional mitochondrial proteome, encompassing mitochondrial proteins and their first interactors. More than 80% of the identified proteins resulted in nodes of this network but with a different ability in coisolating mitochondria-associated structures for each enrichment protocol/cell line pair.Entities:
Keywords: Mitochondrial Human Proteome Project; enrichment protocol; mitochondria; standardization
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Year: 2017 PMID: 28828861 DOI: 10.1021/acs.jproteome.7b00350
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466