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30种抗甲胎蛋白单克隆抗体的特异性和亲和力。

Specificity and affinity of 30 monoclonal antibodies against alpha-fetoprotein.

作者信息

Nustad K, Paus E, Kierulf B, Børmer O P

机构信息

Central Laboratory, Norwegian Radium Hospital, Oslo.

出版信息

Tumour Biol. 1998;19(4):293-300. doi: 10.1159/000030021.

Abstract

Twenty-two antibodies with high affinity for AFP could be classified into groups according to five AFP binding regions, designated A-E, based on cross-inhibition studies and immunometric assay combinations. Antibodies in group A (ISOBM TD2 No. in parentheses): H31 (119), AFP-4-F45 (111), 140/5 (117), K51 (99), K52 (110), AFP-200014A (120) and F2 (118) and in group B: A4-4 (98) and AFP-4-F67 (93) were only inhibited by antibodies belonging to the same groups and could be used in immunometric assay combinations with all other antibodies. Groups C, D and E were inhibited by antibodies in adjacent antibody groups and did not form immunometric assay pairs with antibodies belonging to neighboring groups. Group C comprises: K28 (105), A34-B/B5 (101), AFP-4-F111 (95), AFP100025B (121) and K57 (116), group D: E7 (114) and D10 (92) and group E: H219 (115), K6B1 (103), A34-A/D12 (104), C2 (102), C9 (94) and C10 (97). For six of seven antibodies with low binding to labelled AFP, the specificity could not be determined. Two antibodies were not conclusively assigned to any binding region. Antibody 9A12 (109) may be classified into group E based on immunometric assay combinations, but could not be evaluated in cross-inhibition experiments due to low binding to labelled AFP. Antibody 19F12 (100) functioned as a tracer antibody in combination with all other antibodies, but did not bind AFP when used as solid phase antibody. This antibody could therefore represent a unique binding specificity.

摘要

根据交叉抑制研究和免疫分析组合,对22种与甲胎蛋白(AFP)具有高亲和力的抗体,可依据五个AFP结合区域(命名为A - E)分为不同组。A组(括号内为ISOBM TD2编号)的抗体有:H31(119)、AFP - 4 - F45(111)、140/5(117)、K51(99)、K52(110)、AFP - 200014A(120)和F2(118);B组的抗体有:A4 - 4(98)和AFP - 4 - F67(93),它们仅被同组抗体抑制,可与所有其他抗体用于免疫分析组合。C、D、E组被相邻抗体组中的抗体抑制,且不与相邻组的抗体形成免疫分析对。C组包括:K28(105)、A34 - B/B5(101)、AFP - 4 - F111(95)、AFP100025B(121)和K57(116);D组包括:E7(114)和D10(92);E组包括:H219(115)、K6B1(103)、A34 - A/D12(104)、C2(102)、C9(94)和C10(97)。对于七种与标记AFP结合力低的抗体中的六种,其特异性无法确定。两种抗体未被明确归入任何结合区域。抗体9A12(109)基于免疫分析组合可能归入E组,但由于与标记AFP结合力低,无法在交叉抑制实验中进行评估。抗体19F12(100)与所有其他抗体组合时起示踪抗体的作用,但用作固相抗体时不结合AFP。因此,该抗体可能代表一种独特的结合特异性。

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