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. 2002 May 7;99(10):6913–6918. doi: 10.1073/pnas.102562599

Table 1.

Competition of anti-gp120 mAbs with X5 for gp120JR-FL and gp12089.6

mAb Epitope Env Competition
−sCD4 +sCD4
17b CD4i 89.6 + ++
17b CD4i JR-FL + ++
CG10 CD4i 89.6 0 ++
CG10 CD4i JR-FL 0 +++
A32 CD4i(C1–C4) 89.6 −−−
A32 CD4i(C1–C4) JR-FL −− −−
48d CD4i 89.6 + +
23e CD4i 89.6 + +
21c CD4i 89.6 + +
F91 CD4bs JR-FL + NA
IgG1b12 CD4bs JR-FL + NA
19b V3 JR-FL 0 0
G3-136 V2 JR-FL 0 0
MAG45 C1 JR-FL 0 0
C11 C1–C5 JR-FL 0 0
2G12 C3/V4 JR-FL 0 0
G3–519 C4 JR-FL 0 0
X5 CD4i 89.6 +++ +++

Gp120JR-FL was captured by the anti-gp120 Ab D7324 and incubated with X5 (5 μg/ml) and various antibodies at different concentrations in absence or presence of sCD4 (2 μg/ml), and IgG Fc of the bound antibodies was detected with goat anti-mouse or anti-human IgG Fc alkaline phosphatase conjugate. Gp12089.6 was directly coated on 96-well plates and incubated with biotinylated X5 (0.5 μg/ml) and various antibodies, and the amount of bound X5 was detected by using streptavidin-HRP. +, Denotes some competition; ++, significant competition; +++, complete displacement; −, various degrees of enhancement; 0, lack of measurable effects; NA, not applicable.