TY - JOUR
T1 - State-dependent cross-linking of the M2 and M3 segments
T2 - Functional basis for the alignment of GABAA and acetylcholine receptor M3 segments
AU - Jansen, Michaela
AU - Akabas, Myles H.
PY - 2006
Y1 - 2006
N2 - Construction of a GABAA receptor homology model based on the acetylcholine (ACh) receptor structure is complicated by the low sequence similarity between GABAA and ACh M3 transmembrane segments that creates significant uncertainty in their alignment. We determined the orientation of the GABAA M2 and M3 transmembrane segments using disulfide cross-linking. The M2 residues α1M266 (11′) and α1T267 (12′) were mutated to cysteine in either wild type or single M3 cysteine mutant (α1V297C, α1A300C to α1A305C) backgrounds. We assayed spontaneous and induced disulfide bond formation. Reduction with DTT significantly potentiated GABA-induced currents in α1T267C-L301C and α1T267C-F304C. Copper phenanthroline-induced oxidation inhibited GABA-induced currents in these mutants and in α1T267C-A305C. Intrasubunit disulfide bonds formed between these Cys pairs, implying that the α-carbon separation was at most 5.6 Å. The reactive α1M3 residues (L301, F304, A305) lie on the same face of an α-helix. The unresponsive ones (A300, I302, E303) lie on the opposite face. In the resting state, the reactive side of α1M3 faces M2-α1T267. In conjunction with the ACh structure, our data indicate that alignment of GABAA and ACh M3 requires a single gap in the GABAA M2-M3 loop. In the presence of GABA, oxidation of α1T267C-L301C and α1T267C-F304C had no effect, but oxidation of α1T267C-A305C caused a significant increase in spontaneous channel opening. We infer that, as the channel opens, the distance and/or orientation between M2-α1T267 and M3-α1A305 changes such that the disulfide bond stabilizes the open state. This begins to define the conformational motion that M2 undergoes during channel opening.
AB - Construction of a GABAA receptor homology model based on the acetylcholine (ACh) receptor structure is complicated by the low sequence similarity between GABAA and ACh M3 transmembrane segments that creates significant uncertainty in their alignment. We determined the orientation of the GABAA M2 and M3 transmembrane segments using disulfide cross-linking. The M2 residues α1M266 (11′) and α1T267 (12′) were mutated to cysteine in either wild type or single M3 cysteine mutant (α1V297C, α1A300C to α1A305C) backgrounds. We assayed spontaneous and induced disulfide bond formation. Reduction with DTT significantly potentiated GABA-induced currents in α1T267C-L301C and α1T267C-F304C. Copper phenanthroline-induced oxidation inhibited GABA-induced currents in these mutants and in α1T267C-A305C. Intrasubunit disulfide bonds formed between these Cys pairs, implying that the α-carbon separation was at most 5.6 Å. The reactive α1M3 residues (L301, F304, A305) lie on the same face of an α-helix. The unresponsive ones (A300, I302, E303) lie on the opposite face. In the resting state, the reactive side of α1M3 faces M2-α1T267. In conjunction with the ACh structure, our data indicate that alignment of GABAA and ACh M3 requires a single gap in the GABAA M2-M3 loop. In the presence of GABA, oxidation of α1T267C-L301C and α1T267C-F304C had no effect, but oxidation of α1T267C-A305C caused a significant increase in spontaneous channel opening. We infer that, as the channel opens, the distance and/or orientation between M2-α1T267 and M3-α1A305 changes such that the disulfide bond stabilizes the open state. This begins to define the conformational motion that M2 undergoes during channel opening.
KW - Acetylcholine receptor
KW - Disulfide cross-linking
KW - GABA receptor
KW - Glycine
KW - Ion channel
KW - Serotonin
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U2 - 10.1523/JNEUROSCI.0224-06.2006
DO - 10.1523/JNEUROSCI.0224-06.2006
M3 - Article
C2 - 16641228
AN - SCOPUS:33646828912
SN - 0270-6474
VL - 26
SP - 4492
EP - 4499
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 17
ER -