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. 2001 Feb 27;98(5):2393–2398. doi: 10.1073/pnas.041618598

Table 1.

Reactivity of antibodies with LFA-1 cysteine substitution mutants

mAb % Wild-type binding
K287C/K294C
L289C/K294C
K287C 293T L289C 293T K294C 293T
293T K562 293T K562
BL5 92  ± 11 92 86  ± 16 98 93 92 88
F8.8 94 102 84 94 96 100 95
CBR LFA-1/9 ND 85 ND ND ND ND ND
TS2/6 85  ± 6 89 79  ± 3 96 91 88 92
May.035 93  ± 8 93 82  ± 14 101 96 95 106
TS1/11 94 96 94 105 ND ND ND
TS1/12 89 87 102 106 99 104 94
TS1/22 96  ± 12 93 91  ± 8 110 103 96 92
TS2/14 86  ± 9 95 83  ± 11 103 103 100 103
25.3.1 93 88 91 86 ND ND ND
CBR LFA-1/1 44  ± 1 56 96  ± 8 118 86 93 89
S6F1 89 97 95 86 98 86 92
TS1/18 100  ± 10 97 96  ± 5 106 88 87 108
YFC51 103 101 95 111 ND ND ND
CLBLFA-1/1 ND 96 ND 101 ND ND ND
May.017 ND 109 ND 111 ND ND ND
6.5e ND 84 ND 96 ND ND ND
CBR LFA-1/7 95 95 92 97 ND ND ND
CBR LFA-1/2 ND 86 ND 86 ND ND ND
YTA-1 ND 111 ND 108 ND ND ND

Wild-type or mutant αL and wild-type β2 were coexpressed transiently on the surface of 293T cells or stably on K562 cells. Reactivity with antibodies was determined by flow cytometry. Mean fluorescence of each antibody binding was normalized to the mean fluorescence of mAb TS2/4 binding. The results are expressed as percent of wild-type binding ± difference from the mean. For some antibodies, only one experiment was done. ND, not determined.