Delineating Diseases by IMS-MS Profiling of Serum N-linked Glycans
Altered branching and aberrant expression of N-linked glycans is known to be associated with disease states such as cancer. However, the complexity of determining such variations hinders the development of specific glycomic approaches for assessing disease states. Here, we examine a combination of i...
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Published in | Journal of proteome research Vol. 11; no. 2; pp. 576 - 585 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
03.02.2012
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Subjects | |
Online Access | Get full text |
ISSN | 1535-3893 1535-3907 1535-3907 |
DOI | 10.1021/pr200777u |
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Summary: | Altered branching and aberrant expression of N-linked glycans is known to be associated with disease states such as cancer. However, the complexity of determining such variations hinders the development of specific glycomic approaches for assessing disease states. Here, we examine a combination of ion mobility spectrometry (IMS) and mass spectrometry (MS) measurements, with principal component analysis (PCA) for characterizing serum N-linked glycans from 81 individuals: 28 with cirrhosis of the liver, 25 with liver cancer, and 28 apparently healthy. Supervised PCA of combined ion-mobility profiles for several, to as many as 10 different mass-to-charge ratios for glycan ions, improves the delineation of diseased states. This extends an earlier study [J. Proteome Res. 2008, 7, 1109–1117] of isomers associated with a single glycan (S1H5N4) in which PCA analysis of the IMS profiles appeared to differentiate the liver cancer group from the other samples. Although performed on a limited number of test subjects, the combination of IMS-MS for different combinations of ions and multivariate PCA analysis shows promise for characterizing disease states. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Note: these authors contributed equally. Present address: Texas Tech University, Lubbock, TX 79409 Present address: University of Toledo, OH 43606 Present address: Pacific Northwest National Laboratories, Richland WA 99352 Present address: University of Washington, Saint Louis, MO 63130 |
ISSN: | 1535-3893 1535-3907 1535-3907 |
DOI: | 10.1021/pr200777u |