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. 2018 Dec 11;4(1):20–25. doi: 10.1021/acssensors.8b01381

Table 1. Properties of NB-LUMABS Sensorsa.

Target Sensor name SB1 affinityb SB2 affinityb Cy3 position DR (%) Sensor Kd
Anti-HIV1-p17 HIV-NB-LUMABS-1 Kd = 190 μM Kd = 2.5 μM before SB2 218 ± 12 10.0 ± 0.5 pM
  HIV-NB-LUMABS-2 Kd = 190 μM Kd = 2.5 μM after SB2 177 ± 4 13.7 ± 1.3 pM
  HIV-NB-LUMABS-3 Kd = 190 μM Kd = 2.5 μM before and after SB2 182 ± 18 12.1 ± 0.6 pM
  HIV-NB-LUMABS-4 Kd = 190 μM Kd = 0.18 μM before SB2 138 ± 5 14.2 ± 4.7 pM
  HIV-NB-LUMABS-5 Kd = 190 μM Kd = 190 μM before SB2 252 ± 15 11.7 ± 3.7 pM
  HIV-NB-LUMABS-6 Kd = 2.5 μM Kd = 2.5 μM before SB2 160 ± 3 15.2 ± 1.0 pM
  HIV-NB-LUMABS-7 Kd = 2.5 μM Kd = 0.18 μM before SB2 493 ± 13 11.8 ± 0.5 pM
Cetuximab CTX-NB-LUMABS-1c Kd = 190 μM Kd = 2.5 μM before SB2 233 ± 12 34.7 ± 3.7 nM
  CTX-NB-LUMABS-2c Kd = 190 μM Kd = 2.5 μM after SB2 110 ± 3 20.7 ± 3.4 nM
  CTX-NB-LUMABS-3d Kd = 190 μM Kd = 2.5 μM before SB2 88 ± 2 189 ± 16 nM
a

The measurements were performed in PBS buffer (pH 7.4, 1 mg/mL BSA) with sensor concentration of 1 pM for anti-HIV-p17 and 100 pM for cetuximab.

b

See ref (22).

c

Meditope sequence CVFDLGTRRLRC (monovalent Kd = 61 nM).

d

Meditope sequence CQFDLSTRRLKC (monovalent Kd = 270 nM).