TABLE 2.
MAb | Specificity by FELISA | Specificity by PPTb
|
Concn at 50% bindingc
|
Concn at 50% killingd
|
|||||
---|---|---|---|---|---|---|---|---|---|
MCPS | OAc− | K92 | MCPS | OAc− | K92 | MCPS | OAc− | ||
IgG3κ | |||||||||
2055.5 | MCPS | + | −e | − | 0.2 | −f | − | 0.18 | −g |
2016.3 | OAc− >> MCPS | + | + | − | >3.0 | 0.1 | − | 0.63 | 1.1 |
IgG1κ | |||||||||
C2/1076.10 | MCPS ≈ OAc− >>> K92 | + | + | −h | 0.005 | 0.002 | 1.5 | NDi | ND |
C2/655.7 | OAc− >> MCPS | + | + | − | 0.3 | 0.003 | − | ND | ND |
C2/256.8 | MCPS ≈ OAc− | + | + | − | 0.005 | 0.003 | − | ND | ND |
The fine specificity and precipitation with MCPS and OAc−, the concentration at 50% binding of MAb, and 50% killing were published previously (23, 56).
Determined by Ouchterlony precipitation (PPT) (48). Proteins were tested at 1 mg/ml. +, precipitation; −, no precipitation.
Concentration (micrograms per milliliter) at 50% binding were determined at the midpoint of the linear part of the titration curve on PS-coated plates. Proteins were tested by 12 threefold serial dilutions starting at 3 μg/ml.
The concentration (micrograms per milliliter) of antibody at which 50% of the bacteria were killed.
Not detectable at highest concentration tested (1 mg/ml).
Not detectable at highest concentration tested (3 μg/ml).
No detectable killing.
Negative using the purified protein, but undiluted ascites fluid was positive on all three Ags and negative on K1.
ND, not determined.