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. 2005 May 16;145(7):907–915. doi: 10.1038/sj.bjp.0706252

Table 1.

Inhibition by lipids of [3H]P1075 and [3H]GBC binding to SUR2A and SUR2A(YS) in the presence of MgATP (0.3 mM)

SUR Radioligand LipidM) Binding (% BS) (n)
SUR2A [3H]P1075 PIP2, 100 98±15a (7)
    DOGS-NTA, 100 49±7 (6)
    Oleoyl-CoA, 100 4±1 (4)
    Malonyl-CoA, 300 64±7 (4)
    Oleate, 300 14±3 (3)
SUR2A(YS) [3H]GBC DOGS-NTA, 100 50±4 (6)
    Oleoyl-CoA, 100 38±13 (4)

(n) denotes the number of experiments.

a

At 30 μM PIP2, stimulation of binding to 117±8% was observed.