Glycosylation Analysis of IgLON Family Proteins in Rat Brain by Liquid Chromatography and Multiple-Stage Mass Spectrometry

Satsuki Itoh, Akiko Hachisuka, Nana Kawasaki*§, Noritaka Hashii, Reiko Teshima, Takao Hayakawa, Toru Kawanishi and Teruhide Yamaguchi
Division of Biological Chemistry and Biologicals, National Institute of Health Sciences, 1-18-1, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan, Core Research for Evolutional Science and Technology of Japan Science and Technology Agency, Kawaguchi Center Building, 4-1-8 Hon-cho, Kawaguchi, Saitama 332-0012, Japan, and Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-Osaka 577-8502, Japan
Biochemistry, 2008, 47 (38), pp 10132–10154
DOI: 10.1021/bi8009778
Publication Date (Web): August 26, 2008
Copyright © 2008 American Chemical Society

This work was supported in part by a Grant-in-Aid from the Ministry of Health and Labor and Welfare, and Core Research for Evolutional Science and Technology Program (CREST) of the Japan Science and Technology Agency (JST).

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National Institute of Health Sciences.

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* To whom correspondence should be addressed: Division of Biological Chemistry and Biologicals, National Institute of Health Sciences, 1-18-1, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan. Telephone: +81-3-3700-9074. Fax: +81-3-3707-6950. E-mail: nana@nihs.go.jp.
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§

Core Research for Evolutional Science and Technology of Japan Science and Technology Agency.

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Kinki University.

Abstract

Abstract Image

IgLON family proteins, including limbic-associated membrane protein (LAMP), opioid-binding cell adhesion molecule (OBCAM), neurotrimin, and Kilon, are immunoglobulin (Ig) superfamily cell adhesion molecules. These molecules are composed of three Ig domains and a glycosylphosphatidylinositol (GPI) anchor and contain six or seven potential N-glycosylation sites. Although their glycosylations are supposed to be associated with the development of the central nervous system like other Ig superfamily proteins, they are still unknown because of difficulty in isolating individual proteins with a high degree of homology in performing carbohydrate analysis. In this study, we conducted simultaneous site-specific glycosylation analysis of rat brain IgLON proteins by liquid chromatography and multiple-stage mass spectrometry (LC−MSn). The rat brain GPI-linked proteins were enriched and separated by sodium dodecyl sulfate−polyacrylamide gel electrophoresis. The four proteins were extracted from the gel, and subjected to LC−MSn after proteinase digestions. A set of glycopeptide MS data, including the mass spectrum, the mass spectrum in the selected ion monitoring mode, and the product ion spectra, was selected from all data based on carbohydrate-related ions in the MS/MS spectrum. The peptide portion and the carbohydrate structure were identified on the basis of peptide-related ion and carbohydrate-related ions, and the accurate mass. The site-specific glycosylations of four proteins were elucidated as follows. N-Glycans near the N-terminal were disialic acid-conjugated complex- and hybrid-type oligosaccharides. The first Ig domains were occupied by Man-5-9. Diverse oligosaccharides, including Lewis a/x-modified glycans, a brain-specific glycan known as BA-2, and Man-5, were found to be attached to the third Ig domain. Three common structures of glycans were found in the GPI moiety of LAMP, OBCAM, and neurotrimin.

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History

  • Published In Issue September 23, 2008
  • Article ASAPAugust 26, 2008
  • Received: May 23, 2008
    Revised: July 17, 2008

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