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. 2021 Mar 3;118(10):e2017431118. doi: 10.1073/pnas.2017431118

Table 2.

Characteristics of Glyt1b background constructs

Glyt1b KM (µM) Vmax (pmol/min/mg) Cell surface expression (% of WT) Rate of binding inactivation by MTSEA, M−1 ⋅ sec−1 Rate of binding inactivation by MTSET, M−1 · sec−1 Rate of transport inactivation by MTSET, M−1 · sec−1
WT 35.2 ± 2.1 1560 ± 93 100 3.29 ± 0.09 1.79 ± 0.07 0.61 ± 0.03
C62A 36.4 ± 2.6 1466 ± 81 89.3 ± 5.3 0.40 ± 0.01 0.12 ± 0.01 0.02 ± 0.01
Y60C-C62A 41 ± 4 715 ± 50** 65.3 ± 4.7* nd nd 6.52 ± 0.42
S244C-C62A 35.2 ± 2.8 645 ± 18** 50.7 ± 5.9* 32.10 ± 1.49 20.8 ± 0.70 nd

Transport rates were measured over a range (0.05 to 200 µM) of glycine concentrations, and surface expression was determined by biotinylation as described in Materials and Methods. KM and Vmax values represent the means ± SEM of three experiments for kinetic analysis and four experiments for biotinylation. Sensitivity to MTSEA and MTSET modification was determined from the concentration of methanethiosulfonate reagents and the half-time for inactivation of CHIBA-3007 binding (S244C-C62A) or glycine transport (Y60C-C62A) as described in Materials and Methods. Asterisks indicate significant differences from WT (*P < 0.01, **P < 0.005) using Student’s t test. nd, not determined.