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Please use this identifier to cite or link to this item: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/26989

Title: Arginines in the CDR of anti-dsDNA autoantibodies facilitate cell internalization via electrostatic interactions
Authors: Ying-Chyi Song;Guang-Huan Sun;Tai-Ping Lee;Jason C. Huang;Chia-Li Yu;Chia-Hung Chen;Shye-Jye Tang;Kuang-Hui Sun
Contributors: NTOU:Institute of Bioscience and Biotechnology
國立臺灣海洋大學:生物科技研究所
Keywords: Arginine-rich peptides;Electrostatic interactions;Internalization;Systemic lupus erythematosus
Date: 2008-11
Issue Date: 2011-10-21T02:22:12Z
Publisher: European Journal of Immunology
Abstract: Abstract:Internalization of autoantibodies against double-stranded DNA (anti-dsDNA) is crucial to the pathogenesis of systemic lupus erythematosus. Anti-dsDNA may bind to cell-surface targets in order to facilitate the subsequent cell penetration of the anti-dsDNA. In this study, we observed that the 9D7 monoclonal anti-dsDNA autoantibody (9D7 mAb) penetrates into Jurkat cells via a novel alternative pathway. Endocytosis inhibitors or a lipid-raft inhibitor did not significantly change the penetration of 9D7 mAb into the Jurkat cells. However, heparin sulfate, chondroitin sulfate B, decaarginine and chondroitinase ABC significantly suppressed the internalization and the 9D7 mAb inhibited the internalization of Tat-GFP. Moreover, the penetration of the 9D7 mAb was significantly reduced in proteoglycan-deficient cells (pgs A-745). Positively charged amino acids including arginine are commonly found in the CDR of the 9D7 mAb. Point mutations to the arginine residues in the CDR of the H chain of the recombinant 9D7 mAb significantly attenuated its DNA-binding and cell-penetration abilities. These findings indicate that cell penetration of anti-dsDNA is due to the electrostatic interactions of arginine residues in the CDR with the negatively charged sulfated polysaccharides on the cell surface.
Relation: 38(11), pp.3178–3190
URI: http://ntour.ntou.edu.tw/handle/987654321/26989
Appears in Collections:[生命科學暨生物科技學系] 期刊論文

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