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Characteristic glycopeptides associated with extreme human longevity identified through plasma glycoproteomics
Authors:Yuri Miura  Noritaka Hashii  Yuki Ohta  Yoko Itakura  Hiroki Tsumoto  Junya Suzuki  Daisuke Takakura  Yukiko Abe  Yasumichi Arai  Masashi Toyoda  Nana Kawasaki  Nobuyoshi Hirose  Tamao Endo
Institution:1. Research Team for Mechanism of Aging, Tokyo Metropolitan Institute of Gerontology, 35-2 Sakae-cho, Itabashi-ku, Tokyo 173-0015, Japan;2. Division of Biological Chemistry and Biologicals, National Institute of Health Sciences, 3-25-26 Tono-machi, Kawasaki-ku, Kawasaki-shi 210-9501, Kanagawa, Japan;3. Research Team for Geriatric Medicine, Tokyo Metropolitan Institute of Gerontology, 35-2 Sakae-cho, Itabashi-ku, Tokyo 173-0015, Japan;4. Center for Supercentenarian Medical Research, Keio University School of Medicine, 35 Shinano-machi, Shinjuku-ku, Tokyo 160-8582, Japan
Abstract:

Background

Glycosylation is highly susceptible to changes of the physiological conditions, and accordingly, is a potential biomarker associated with several diseases and/or longevity. Semi-supercentenarians (SSCs; older than 105?years) are thought to be a model of human longevity. Thus, we performed glycoproteomics using plasma samples of SSCs, and identified proteins and conjugated N-glycans that are characteristic of extreme human longevity.

Methods

Plasma proteins from Japanese semi-supercentenarians (SSCs, 106–109?years), aged controls (70–88?years), and young controls (20–38?years) were analysed by using lectin microarrays and liquid chromatography/mass spectrometry (LC/MS). Peak area ratios of glycopeptides to corresponding normalising peptides were subjected to orthogonal projections to latent structures discriminant analysis (OPLS-DA). Furthermore, plasma levels of clinical biomarkers were measured.

Results

We found two lectins such as Phaseolus vulgaris, and Erythrina cristagalli (ECA), of which protein binding were characteristically increased in SSCs. Peak area ratios of ECA-enriched glycopeptides were successfully discriminated between SSCs and controls using OPLS-DA, and indicated that tri-antennary and sialylated N-glycans of haptoglobin at Asn207 and Asn211 sites were characterized in SSCs. Sialylated glycans of haptoglobin are a potential biomarker of several diseases, such as hepatocellular carcinoma, liver cirrhosis, and IgA-nephritis. However, the SSCs analysed here did not suffer from these diseases.

Conclusions

Tri-antennary and sialylated N-glycans on haptoglobin at the Asn207 and Asn211 sites were abundant in SSCs and characteristic of extreme human longevity.

General significance

We found abundant glycans in SSCs, which may be associated with human longevity.
Keywords:ALB  albumin  ANOVA  analysis of variance  CRP  C-reactive protein  ECA  GOT  glutamic oxaloacetic transaminase  GPT  glutamic pyruvic transaminase  γGTP  γ-glutamyl transpeptidase  HB  haemoglobin  HCC  hepatocellular carcinoma  IL-6  interleukin-6  LC  liver cirrhosis  LC/MS  liquid chromatography/mass spectrometry  OPLS-DA  orthogonal projections to latent structures discriminant analysis  PHAL  PLT  platelet  RBC  red blood cell  SSCs  semi-supercentenarians  TNF-α  tumour necrosis factor-α  TP  total protein  WBC  white blood cell  Lectin microarray  LC/MS  Longevity  Semi-supercentenarian
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