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. 2017 Jun 1;12(6):e0178885. doi: 10.1371/journal.pone.0178885

Table 3. IC50 (pM) of insulin, IGF1 and IGF2 to position 718 mutated full length receptors.

Receptor Insulin IC50 (pM)
Geometric mean (95% confidence intervals)
IGF1 IC50 (pM)
Geometric mean (95% confidence intervals)
IGF2 IC50 (pM)
Geometric mean (95% confidence intervals)
IR-A 16.0 (7.2 to 35.6) 705 (363 to 1371) 95 (48 to 188)
IR-A P718A 15.1 (9.8 to 23.4) 1374 (1065 to 1773) 218 (151 to 316)
IR-A P718E 20.2 (8.9 to 45.9) 1059 (799 to 1404)* 154 (83 to 282)*
IR-A P718K 16.3 (10.2 to 26.0) 3672 (1591 to 8474)* 595 (240 to 1475)*
IR-B 13.0 (9.8 to 17.3) 4360 (2540 to 7486) 477 (259 to 877)
IR-B K718A 15.2 (7.4 to 31.1) 3622 (1603 to 8185) 288 (160 to 517)*
IR-B K718E 12.8 (10.1 to 16.7) 1496 (831 to 2693)* 225 (123 to 411)*
IR-B K718P 11.9 (7.6 to 18.7) 927 (429 to 2005)* 155 (78 to 311)*

The affinities of human insulin, IGF1 and IGF2 to IR-A, IR-B and position 718 mutated full length receptors were determined in SPA binding assay with displacement of 125I-insulin. The geometric mean of IC50 (pM) and the 95% confidence intervals are given for n = 3–5 independent experiments.

*) Significant difference (p < 0.05) determined by T-test between WT and mutant.