| Literature DB >> 25418953 |
Sandra Isabel Anjo1, Cátia Santa, Bruno Manadas.
Abstract
The quantification of large proteomes across multiple samples has become the major focus of proteomics. In addition to the advantages of in-gel digestion, the extensive time and sample handling required have precluded the use of this type of method for large quantitative screens. Therefore, an adaptation of the in-gel digestion method, termed short-GeLC, is proposed as a faster and more reproducible sample preparation method for quantitative approaches. The proposed methodology was compared with two well-established procedures for sample preparation, GeLC-MS and the classic liquid digestion followed by LC-MS, using a membrane protein-enriched sample. The results show that the short-GeLC approach substantially reduces the amount of sample handling and the overall time required for analysis compared with the gel-based methods without compromising the overall results at the protein identification level. Furthermore, the short-GeLC approach in combination with the SWATH acquisition method leads to the best quantitative results: more proteins were quantified, and the reproducibility was improved. Finally, this method performed well even on challenging samples enriched in membrane proteins.Keywords: In-gel digestion; Membrane proteins; Proteomic screenings; Quantification; SWATH; Technology
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Year: 2015 PMID: 25418953 DOI: 10.1002/pmic.201400221
Source DB: PubMed Journal: Proteomics ISSN: 1615-9853 Impact factor: 3.984