Monoclonal antibodies defining blood group A variants with difucosyl type 1 chain (ALeb) and difucosyl type 2 chain (ALey).
Monoclonal antibodies defining blood group A variants with difucosyl type 1 chain (ALeb) and difucosyl type 2 chain (ALey).
复制标题
使用二岩藻糖基 1 型链 (ALeb) 和二岩藻糖基 2 型链 (ALey) 定义 A 型血型变体的单克隆抗体。
DOI:
10.1021/bi00343a024
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发表时间:
1985
期刊:
影响因子:
2.9
通讯作者:
Hakomori,S
中科院分区:
文献类型:
--
作者:
Clausen,H;McKibbin,JM;Hakomori,S
Program of Biochemical Oncology/Membrane Research, Fred Hutchinson Cancer Research Center, and Departments of Pathobiology, Microbiology, and Immunology, University of Washington, Seattle, Washington 98104, and Department of Biochemistry, University of Alabama at Birmingham, Birmingham, Alabama 35294 Received April 12, 1985 abstract: Three hybridomas secreting monoclonal antibodies, HH1, HH2, and HH3, defining different difucosyl A structures (ALeb or ALey), have been established. Antibody HH1 (IgG2a) reacts specifically with the difucosyl A structure irrespective of a type 1 or type 2 chain, while antibody HH2 (IgG3) reacts exclusively with the difucosyl type 2 chain A (ALey) and does not react with the difucosyl type 1 chain or monofucosyl type 2 chain. Antibody HH3 (IgG2a) reacts exclusively with the difucosyl type 1 chain A (ALeb) and does not react with the monofucosyl type 1 chain A or mono- and difucosyl type 2 chain A. These hybridoma antibodies were obtained by immunization of mice with purified glycolipid antigens and were selected by their reactivity with the specific glycolipid structures. These antibodies, together with previously established monoclonal antibody AH-21, specific for monofucosyl type 1 chain A, and monoclonal antibody TH-1, specific for type 3 chain A, are extremely usefulto define blood group A variants present in cells and tissues. e blood group A determinant is a well-established tri-saccharide, GalN Aca 1—3 [Fuca 1-* 2] Gal/31—>-R; however, the determinant is carried by a large number of core structures as listed in Table I [reviewed by Watkins (1980) and Hakomori (1981)]. With therecent development of the monoclonal antibody approach, the complexity and variation in blood group