Table 1.

Epitope mapping and identification of the relative affinity for each Psl mAb

Epitope mAb Kd Phage library Cell attachment max. inhibition OPK EC50 
  nM  µg/ml µg/ml 
Class 1 Cam-003 144.00 Naive 1.0 0.0220 
 Cam-004 2,100.00 Naive >30.0 0.2771 
 Cam-005 8,400.00 Naive >30.0 >30.0 
Class 2 WapR-001 0.84 Patient 30.0 0.3100 
 WapR-003 12.20 Patient 30.0 0.2778 
 WapR-002 12.60 Patient 30.0 0.3960 
Class 3 WapR-016 75.00 Patient 10.0 0.2417 
Epitope mAb Kd Phage library Cell attachment max. inhibition OPK EC50 
  nM  µg/ml µg/ml 
Class 1 Cam-003 144.00 Naive 1.0 0.0220 
 Cam-004 2,100.00 Naive >30.0 0.2771 
 Cam-005 8,400.00 Naive >30.0 >30.0 
Class 2 WapR-001 0.84 Patient 30.0 0.3100 
 WapR-003 12.20 Patient 30.0 0.2778 
 WapR-002 12.60 Patient 30.0 0.3960 
Class 3 WapR-016 75.00 Patient 10.0 0.2417 

Epitope mapping was performed by competition ELISA and confirmed using an Octet flow system with Psl derived from the supernatant of an overnight culture of PAO1. The results indicate that Psl antibodies bind to at least three epitopes, which we refer to as class I, II, and III. Class I and II antibodies do not compete for binding; however, the class III antibody, WapR-016, partially inhibits binding of the class I and II antibodies. Antibody affinity was determined by Octet binding assays using Psl derived from the supernatant of overnight PAO1 cultures. Antibody KD was determined by averaging the binding kinetics of seven concentrations for each antibody. Also shown is a summary of cell attachment and OPK data experiments for each antibody. ELISA and antibody affinity was determined using three independent studies.

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