Source:http://linkedlifedata.com/resource/pubmed/id/17949060
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
22
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pubmed:dateCreated |
2007-11-16
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pubmed:abstractText |
The first method of isotopic substitution of a nonbridging oxygen atom in pre-existing phosphates on peptides is reported, solving a long-standing, challenging issue in the sample preparation of phosphopeptides. Peptidyl phosphates, phosphate groups on phosphopeptides, are converted to phosphoramidates with carbodiimide assistance. Acid-catalyzed hydrolysis of the newly formed phosphoramidates incorporates one oxygen atom from H2(16)O or H2(18)O, producing peptidyl phosphates-16O1 or -18O1, respectively. The oxygen labels are stable under common separation and analysis conditions. This labeling method causes minimal structural alteration to peptidyl phosphates and allows the direct application of established phosphate-specific marker ions to the mass spectrometric analysis of differentially labeled phosphopeptide pairs. Using phosphotyrosinyl peptides as model analytes, the characteristic 16O1- and 18O1-labeled phosphotyrosine immonium ions at m/z 216.043 and 218.047 are used for developing a method of phosphopeptide quantitation that is independent of the amino acid sequence of the peptides. From analysis by tandem parallel fragmentation mass spectrometry, it is clear that the phosphate-specific marker ions authentically inherit the quantitative information from precursor phosphopeptides. The dynamic range for relative quantitation of differentially labeled phosphopeptides is at least 2 orders of magnitude for experiments run on a quadrupole time-of-flight mass spectrometer. The use of 16O1 and 18O1 labeling for counting the number of phosphate groups on peptides is also demonstrated.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Carbodiimides,
http://linkedlifedata.com/resource/pubmed/chemical/Ions,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygen Isotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphates,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphotyrosine
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0003-2700
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
79
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
8454-62
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pubmed:meshHeading |
pubmed-meshheading:17949060-Acids,
pubmed-meshheading:17949060-Carbodiimides,
pubmed-meshheading:17949060-Hydrolysis,
pubmed-meshheading:17949060-Ions,
pubmed-meshheading:17949060-Kinetics,
pubmed-meshheading:17949060-Mass Spectrometry,
pubmed-meshheading:17949060-Molecular Structure,
pubmed-meshheading:17949060-Oxygen Isotopes,
pubmed-meshheading:17949060-Phosphates,
pubmed-meshheading:17949060-Phosphopeptides,
pubmed-meshheading:17949060-Phosphorylation,
pubmed-meshheading:17949060-Phosphotyrosine
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pubmed:year |
2007
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pubmed:articleTitle |
Oxygen isotopic substitution of peptidyl phosphates for modification-specific mass spectrometry.
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pubmed:affiliation |
Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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