http://www.cnr.it/ontology/cnr/individuo/prodotto/ID56064
Extraction methods of red blood cell membrane proteins for Multidimensional Protein Identification Technology (MudPIT) analysis. (Articolo in rivista)
- Type
- Label
- Extraction methods of red blood cell membrane proteins for Multidimensional Protein Identification Technology (MudPIT) analysis. (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.chroma.2010.06.045 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- De Palma A; Roveri A; Zaccarin M; Benazzi L; Daminelli S; Pantano G; Buttarello M; Ursini F; Gion M; Mauri PL. (literal)
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- 1. CNR, ITB, Prote & Metabol Unit, I-20090 Milan, Italy
2. Univ Padua, Dept Biol Chem, I-35131 Padua, Italy
3. IRCCS, IOV, I-35131 Padua, Italy
4. Univ Padua, Azienda Osped, Dept Lab Med, I-35131 Padua, Italy
5. Reg Hosp, Consortium Ist Oncol Veneto IRCCS, Ctr Study Biol Markers Malignancy, Venice, Italy (literal)
- Titolo
- Extraction methods of red blood cell membrane proteins for Multidimensional Protein Identification Technology (MudPIT) analysis. (literal)
- Abstract
- Since red blood cells (RBCs) lack nuclei and organelles, cell membrane is their main load-bearing component and, according to a dynamic interaction with the cytoskeleton compartment, plays a pivotal role in their functioning. Even if erythrocyte membranes are available in large quantities, the low abundance and the hydrophobic nature of cell membrane proteins complicate their purification and detection by conventional 20 gel-based proteomic approaches. So, in order to increase the efficiency of RBC membrane proteome identification, here we took advantage of a simple and reproducible membrane sub-fractionation method coupled to Multidimensional Protein Identification Technology (MudPIT). In addition, the adoption of a stringent RBC filtration strategy from the whole blood, permitted to remove exhaustively contaminants, such as platelets and white blood cells, and to identify a total of 275 proteins in the three RBC membrane fractions collected and analysed. Finally, by means of software for the elaboration of the great quantity of data obtained and programs for statistical analysis and protein classification, it was possible to determine the validity of the entire system workflow and to assign the proper sub-cellular localization and function for the greatest number of the identified proteins. (C) 2010 Elsevier B.V. All rights reserved. (literal)
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