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Submitted on November 9, 2006
Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata 997-0017
Corresponding Author: y-ishi{at}ttck.keio.ac.jp
We have developed novel methods for phosphopeptide enrichment using aliphatic hydroxy acid-modified metal oxide chromatography (MOC). Titania and zirconia were successfully applied to enrich phosphopeptides with the aid of aliphatic hydroxy acids, such as lactic acid and beta-hydroxypropanoic acid (HPA), to reduce the interaction between acidic non-phosphopeptides and the metal oxides. These methods removed the vast majority of non-phosphopeptides from phosphoprotein standard digests, and large numbers of phosphopeptides could be readily identified. The methods were coupled with nanoLC-MS/MS systems without difficulty. Recovery of phosphopeptides in MOC varied greatly from peptide to peptide, ranging from a few percent to 100% and the average was almost 50%. Repeatability and linearity were satisfactory. In an examination of the cytoplasmic fraction of HeLa cells, more than 1000 phosphopeptides were identified using lactic acid-modified titania-MOC and HPA-modified zirconia-MOC, respectively. The overlap between phosphopeptides enriched by these two methods was 40% and the combined results provided 1646 unique phosphopeptides. To our knowledge, this is the first successful application of a single MOC-based approach to phosphopeptide enrichment from complex biological samples such as cell lysates.
Revised on February 21, 2007
Accepted on February 22, 2007
Phosphopeptide enrichment by aliphatic hydroxy acid-modified metal oxide chromatography for NanoLC-MS/MS in proteomics applications
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