CALCULATION OF THE AFFINITY CONSTANT K(ASS) FOR SOLID-PHASE ANTIGEN - A MODEL SYSTEM USING MONOCLONAL-ANTIBODIES AGAINST THE CAT ALLERGEN FEL-D-I

被引:5
作者
VANMILLIGEN, FJ
VANETTEN, L
AALBERSE, RC
机构
[1] NETHERLANDS RED CROSS,BLOOD TRANSFUS SERV,CENT LAB,PUBLICAT SECRETARIAT,POB 9406,1006 AK AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,EXPTL & CLIN IMMUNOL LAB,AMSTERDAM,NETHERLANDS
关键词
AFFINITY CONSTANT; SOLID-PHASE ANTIGEN; FEL-D-I; MONOCLONAL ANTIBODY;
D O I
10.1016/0022-1759(93)90381-G
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this report a procedure is described to calculate the affinity constant of an antibody for solid-phase Ag. K(SP) (K(ASS) solid phase) was defined as the reciprocal of the concentration of Ag required for half saturation of the Ab-binding sites, extrapolated to an infinitely small concentration of Ab (semi-saturation plot). Using this procedure, the affinity of IgE antibodies can be measured without interference from 'invisible' IgG antibodies. As a model system, mAbs against the cat allergen Fel d I were used. Serial dilutions of Fel d I-Sepharose were incubated with serial dilutions of mAb Fd1a and Fd1b, with or without rabbit antibodies as 'invisible' antibodies. The Ab-binding capacity of Sepharose-coupled Fel d I was low: 4.15% and 2.13% of the expected value for mAb Fd1a and Fd1b, respectively, and this must be taken into account when calculating K(SP). The K values of mAb Fd1a and Fd1b, calculated from the y axis intercept of the semi-saturation plot, were 85 (pmol/test)-1 and 65 (pmol/test)-1 respectively. Using the semi-saturation plot, K(SP) of mAb Fd1a was not affected by the presence of rabbit antibodies against Fel d I. confirming the applicability of the procedure for measuring the K(SP) of IgE in patient sera. For one cat-allergic patient the K(SP) of IgE and IgG4 for Fel d I were calculated and found to be 62 (pmol/test)-1 and 147 (pmol/test)-1 for IgE and IgG4 respectively.
引用
收藏
页码:165 / 173
页数:9
相关论文
共 19 条
[12]   DIRECT MEASUREMENT OF ANTIBODY-AFFINITY DISTRIBUTION BY HAPTEN-INHIBITION ENZYME-IMMUNOASSAY [J].
NIETO, A ;
GAYA, A ;
JANSA, M ;
MORENO, C ;
VIVES, J .
MOLECULAR IMMUNOLOGY, 1984, 21 (06) :537-543
[13]   INFLUENCE OF ANTIBODY-AFFINITY ON THE PERFORMANCE OF DIFFERENT ANTIBODY-ASSAYS [J].
NIMMO, GR ;
LEW, AM ;
STANLEY, CM ;
STEWARD, MW .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 72 (01) :177-187
[14]  
PERSSON MAA, 1988, J IMMUNOL, V140, P3875
[15]   AN INHIBITION ENZYME-IMMUNOASSAY FOR ESTIMATING RELATIVE ANTIBODY-AFFINITY AND AFFINITY HETEROGENEITY [J].
RATH, S ;
STANLEY, CM ;
STEWARD, MW .
JOURNAL OF IMMUNOLOGICAL METHODS, 1988, 106 (02) :245-249
[16]  
STEWARD MW, 1972, IMMUNOLOGY, V22, P747
[17]   ESTIMATION OF THE AVIDITY OF ANTIBODIES IN POLYCLONAL ANTISERA AGAINST STREPTOCOCCUS-PNEUMONIAE TYPE-3 BY INHIBITION ELISA [J].
VANDAM, GJ ;
VERHEUL, AFM ;
ZIGTERMAN, GJWJ ;
DEREUVER, MJ ;
SNIPPE, H .
MOLECULAR IMMUNOLOGY, 1989, 26 (03) :269-274
[18]   A SIMPLE METHOD FOR RANKING THE AFFINITIES OF MONOCLONAL-ANTIBODIES [J].
VANHEYNINGEN, V ;
BROCK, DJH ;
VANHEYNINGEN, S .
JOURNAL OF IMMUNOLOGICAL METHODS, 1983, 62 (02) :147-153
[19]   EFFECT OF ANTIBODY-AFFINITY ON THE ISOTHERM OF ANTIBODY-BINDING TO SURFACE-IMMOBILIZED ANTIGEN [J].
WERTHEN, M ;
NYGREN, H .
JOURNAL OF IMMUNOLOGICAL METHODS, 1988, 115 (01) :71-78