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M2 delta, a candidate for the structure lining the ionic channel of the nicotinic cholinergic receptor.

作者信息

Oiki S, Danho W, Madison V, Montal M

机构信息

Roche Institute of Molecular Biology, Nutley, NJ 07110.

出版信息

Proc Natl Acad Sci U S A. 1988 Nov;85(22):8703-7. doi: 10.1073/pnas.85.22.8703.

DOI:10.1073/pnas.85.22.8703
PMID:2460876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC282529/
Abstract

A synthetic 23-mer peptide that mimics the sequence of the putative transmembrane M2 segment of the Torpedo californica acetylcholine receptor (AcChoR) delta subunit--Glu-Lys-Met-Ser-Thr-Ala-Ile-Ser-Val-Leu-Leu-Ala-Gln-Ala-Val-Phe-Leu- Leu-Leu-Thr-Ser-Gln-Arg--forms discrete ionic channels in phosphatidylcholine bilayers. In contrast, a synthetic peptide that mimics the sequence of the putative M1 transmembrane segment of the Torpedo AcChoR delta subunit--Leu-Phe-Tyr-Val-Ile-Asn-Phe-Ile-Thr-Pro-Cys-Val-Leu-Ile-Ser-Phe- Leu-Ala-Ser-Leu-Ala-Phe-Tyr--does not form channels. The synthetic M2 delta channel peptide exhibits features that are characteristic of the authentic AcChoR channel, such as single channel conductances, discrimination of cations over anions, and channel lifetimes for open and closed states in the millisecond time range. Energetic considerations suggest that an aggregate of five amphipathic alpha-helices conforms the channel. Thus, the M2 segment may be a component of the AcChoR channel structure.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a344/282529/d60396e6330c/pnas00301-0343-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a344/282529/d60396e6330c/pnas00301-0343-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a344/282529/d60396e6330c/pnas00301-0343-a.jpg

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本文引用的文献

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Primary structures of beta- and delta-subunit precursors of Torpedo californica acetylcholine receptor deduced from cDNA sequences.从cDNA序列推导的加州电鳐乙酰胆碱受体β和δ亚基前体的一级结构。
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Nucleotide and deduced amino acid sequences of Torpedo californica acetylcholine receptor gamma subunit.加州电鳐乙酰胆碱受体γ亚基的核苷酸及推导的氨基酸序列
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