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Table 3 Binding of mAbs to subtype-A, B and C derived HIV-1 proteins and peptides

From: Production and characterization of human anti-V3 monoclonal antibodies from the cells of HIV-1 infected Indian donors

 

2anti-V3 mAbs

 

1Protein/peptide

Subtype

I277

I903

I904

A447-52D

1418

Con-C V3

C

0.33

0.109

0.046

1.2

>10

Con-B V3

B

>10

>10

0.623

0.323

>10

Du156.12

C

0.047

0.019

0.009

0.035

>10

JRFL

B

>10

>10

0.04

0.01

>10

92RW020

A

0.098

0.05

0.028

0.323

>10

SF162

B

>10

>10

>10

0.004

>10

MN

B

>10

>10

2.27

0.011

>10

MPER

C

>10

>10

>10

>10

>10

IDR

C

>10

>10

>10

>10

>10

p24

B

>10

>10

>10

>10

>10

BSA

NA

>10

>10

>10

>10

>10

PP

NA

>10

>10

>10

>10

>10

  1. 1List of recombinant proteins and peptides derived from subtype-A, B and C HIV-1 viruses, NA: Not applicable.
  2. 2Four anti-V3 antibodies, three from IndianI (277, 903 and 904) and one from AmericanA (447-52D) HIV-1 infected donor were tested for their relative binding. The binding activity of anti-V3 mAbs against proteins and peptides was tested by ELISA using mAbs at a concentration ranging from 10 to 0.00003 μg/ml (12 dilutions). The 50% binding titers (Max50, conc. μg/ml) of each antibody against the corresponding protein or peptide is depicted as numerical values in Bold (high affinity), Italic (low affinity) and >10, where Max50 value was not reached. Human anti-parvovirus B19 mAb 1418 was used as negative control. Each experiment was performed at least two independent times.