Characterization of anti-Tn-antigen MLS128 binding proteins involved in inhibiting the growth of human colorectal cancer cells
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- Zamri Normaiza
- Department of Applied Biochemistry, Tokai University School of Engineering
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- Masuda Naoya
- Department of Applied Biochemistry, Tokai University School of Engineering
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- Oura Fumie
- Department of Applied Biochemistry, Tokai University School of Engineering
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- Kabayama Kazuya
- Institute of Glycoscience, Tokai University
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- Yajima Yukiko
- Department of Applied Biochemistry, Tokai University School of Engineering
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- Nakada Hiroshi
- Department of Molecular Bioscience, Faculty of Life Sciences, Kyoto Sangyo University
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- Yamamoto Kazuo
- Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo
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- Fujita-Yamaguchi Yoko
- Department of Applied Biochemistry, Tokai University School of Engineering
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抄録
MLS128 monoclonal antibody, which binds an epitope consisting of two or three consecutive Tn-antigens, inhibits colon cancer cell growth by binding to a 110 kDa glycoprotein (GP). Previous studies suggested a possible association of insulin-like growth factor-I receptor (IGF-IR) signaling in the inhibition of colon cancer cell growth by MLS128 (Morita et al. Biosci Trends. 3, 32-37, 2009; Zamri et al. ibid. 6, 303-312, 2012). The current study thus investigated the nature of 110 kDa GP and its possible association with IGF-IR. MLS128 treatment for 3 days caused down-regulation of IGF-IR and disappearance of 110 kDa GP in HT29 colon cancer cells. Immunoprecipitation/immunoblotting experiments did not reveal a direct association between the two molecules in HT29 cells. In LS180 and HT29 cells, however, 110 kDa GP and IGF-IR were found in microdomains. Treatment of these cells with MLS128 for 3 days caused a reduction in the IGF-IR and 110 kDa GP associated with microdomains. Two-dimensional gel electrophoresis/MLS128 immunoblotting of HT29 and LS180 cell lysates and immunoprecipitates revealed three spots, from which tryptic peptides were recovered for protein sequencing. Identification of 110 kDa GP was unsuccessful due to its heterogeneity and resistance to tryptic digestion. During this study, however, limited proteolysis of 110 kDa GP was observed in the microdomain-associated 110 kDa GP from HT29 and LS180 cells, suggesting that protease-susceptible sites or domains exist in the middle of 110 kDa GP. This information on limited proteolysis may provide a clue to identifying 110 kDa GP.
収録刊行物
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- BioScience Trends
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BioScience Trends 7 (5), 221-229, 2013
特定非営利活動法人 バイオ＆ソーシャル・サイエンス推進国際研究交流会