Glycan Imaging Mass Spectrometry: Progress in Developing Clinical Diagnostic Assays for Tissues, Biofluids, and Cells.
Glycan Imaging Mass Spectrometry: Progress in Developing Clinical Diagnostic Assays for Tissues, Biofluids, and Cells.
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DOI:
10.1016/j.cll.2021.03.005
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发表时间:
2021-06
影响因子:
1.7
通讯作者:
Drake RR
中科院分区:
文献类型:
--
作者:
Blaschke CRK;McDowell CT;Black AP;Mehta AS;Angel PM;Drake RR
Protein glycosylation is a highly prevalent post-translational modification involving the attachment of oligosaccharides, most commonly to a serine/threonine residue (O-linked glycosylation) or an asparagine residue (N-linked glycosylation). Glycosylation is a highly regulated process with over 300 enzymes involved in their biosynthesis and processing in a non-template driven manner. This is done by a series of sequential reactions involving a wide array of glycotransferases that attach single monosaccharides from nucleotide sugar donors, as well as different glycosidases that remove individual monosaccharides. 1 The expression, activity, and localization of these enzymes are sensitive to the physiological state of the cell. Estimated to occur on over half of human proteins, 2 N-linked glycosylation has essential roles in protein folding, molecular trafficking, signal transduction, cell-cell interactions, and many other processes. 3-6 Glycans serve as one of the initial points of contact during cell to cell interactions, so therefore disease changes in glycan biosynthesis can be more apparent than disease related changes associated with gene mutations and proteins. 7 Alterations in N-linked glycosylation have been found in a variety of diseases, including but not limited to cancer, 8 inflammatory arthritis, 9 liver fibrosis/cirrhosis, 10 schizophrenia, 11 type 2 diabetes, 12 ischemic stroke, 13 and Parkinson’s disease. 14 Particularly for cancers, the majority of FDA-approved cancer biomarkers are comprised of circulating glycoproteins or carbohydrate antigens for measurement in blood. 7, 8, 15-18 Glycoproteins can be ideal biomarkers because they enter circulation from tissues or blood cells through active
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