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. Author manuscript; available in PMC: 2010 Jan 14.
Published in final edited form as: J Neurosci. 2009 Jan 28;29(4):907–917. doi: 10.1523/JNEUROSCI.4081-08.2009

Table I.

Summary of D-serine concentration-response data and potentiation by extracellular Ca2+ at GluRδ2Lc mutants.

D-serine + 0 mM Ca2+ D-serine + 3 mM Ca2+ Fold shift Ca2+
potentiation
(relative to
baseline)
GluRδ2Lc
mutant
EC50 (μM) nH N EC50 (μM) nH N EC50
3mM / 0mM
GluRδ2Lc 309 ± 8 1.0 12 2720 ± 90 2.1 10 8.8 3.8 ± 0.23
R530K n.d. n.d. n.d. 3.3 ± 0.20
D742A n.d. n.d. n.d. 3.5 ± 0.11
E531A 319 ± 10 1.1 8 705 ± 55 1.9 8 2.2 1.6 ± 0.08
D535A 1600 ± 80 2.3 10 1580 ± 240 2.2 8 1.0 1.0 ± 0.01
D782A 278 ± 11 1.0 12 304 ± 18 1.1 8 1.1 0.8 ± 0.02
E531A+D535A 10200 ± 1000 2.2 10 8770 ± 630 2.2 12 0.9 1.0 ± 0.04
E531A+D782A 8240 ± 180 2.3 5 7540 ± 140 2.4 6 0.9 0.9 ± 0.04
D535A+D782A 345 ± 31 1.0 6 351 ± 6 1.1 5 1.0 0.6 ± 0.01
E531C+D782C 1170 ± 180 0.8 6 897 ± 212 0.8 6 0.8 0.9 ± 0.01
D535C+D782C 472 ± 99 0.9 6 514 ± 90 1.0 4 1.1 0.9 ± 0.01
P528C+L789C 898 ± 192 1.1 7 1070 ± 200 0.8 4 1.2 0.9 ± 0.01

D-serine EC50 ± SEM in the presence and absence of extracellular Ca2+were used to calculate the fold shift in D-serine EC50. N is the number of oocytes used to generate the data, nH is the Hill slope, and n.d. indicates not determined. Ca2+ potentiation is the fold potentiation ± SEM of baseline spontaneously active GluRδ2Lc currents by the application of 3 mM Ca2+.