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. 2018 Mar 13;9(2):e00036-18. doi: 10.1128/mBio.00036-18

TABLE 1 .

MAb MN86-994-11 binds with high affinity (subnanomolar KD) to both subfamily A and B fHBP variantsa

fHBP variant
(% identity)
Value (error)
KD (M) kon (1/Ms) koff (1/s)
A05 (100) 2.29E-11 (<1E-12) 3.02E+5 (2.77E+2) 6.92E-6 (6.52E-8)
A12 (85) 1.73E-11 (<1E-12) 4.09E+5 (1.27E+3) 7.06E-6 (1.94E-7)
A22 (89) 8.64E-11 (<1E-12) 2.07E+5 (2.22E+2) 1.79E-5 (9.02E-8)
A29 (93) 7.36E-11 (<1E-12) 2.22E+5 (3.51E+2) 1.63E-6 (1.37E-7)
B01 (100) 5.73E-11 (<1E-12) 3.12E+5 (2.28E+2) 1.79E-5 (6.77E-8)
B09 (88) 1.25E-11 (<1E-12) 2.30E+5 (2.86E+2) 2.88E-6 (1.08E-7)
B24 (87) 2.58E-11 (<1E-12) 2.57E+5 (3.30E+2) 6.62E-6 (8.89E-8)
B44 (91) 1.50E-10 (<1E-12) 8.28E+5 (4.76E+3) 1.24E-4 (5.95E-7)
a

The affinity of MN86-994-11-1 for fHBP was determined with the Octet RED96 system. Four nonlipidated recombinant subfamily A variants (A05, A12, A22, and A29) and four nonlipidated subfamily B variants (B01, B09, B24, and B44) were tested. The percent amino acid sequence identities of fHBP variants to vaccine antigens A05 and B01 are indicated.