4.4 Article

Assessing the lipid requirements of the Torpedo californica nicotinic acetylcholine receptor

期刊

BIOCHEMISTRY
卷 45, 期 13, 页码 4327-4337

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AMER CHEMICAL SOC
DOI: 10.1021/bi052281z

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  1. NINDS NIH HHS [R01 NS043438, NS43438, R01 NS043438-04] Funding Source: Medline

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The lipid requirements of the Torpedo californica nicotinic acetylcholine receptor (nAChR) were assessed by reconstituting purified receptors into lipid vesicles of defined composition and by using photolabeling with 3-trifluoromethy 1-3-(m-[I-125]iodophenyl)diazirine ([I-125]TID) to determine functionality. Earlier studies demonstrated that nAChRs reconstituted into membranes containing phosphatidylcholine (PC), the anionic lipid phosphatidic acid (PA), and cholesterol (CH) are particularly effective at stabilizing the nAChR in the resting (closed) state that is capable of undergoing agonist-induced conformational transitions (i.e., functionality). The present studies demonstrate that (1) there is no obligatory requirement for PC, (2) increasing the CH content serves to increase the degree to which nAChRs are stabilized in the resting state, and this effect Saturates at similar to 35 mol % (molar lipid percentage), and (3) the effect of increasing levels of PA saturates at similar to 12 mol % and in the absence of PA nAChRs are stabilized in the desensitized state (i.e., nonfunctional). Native Torpedo membranes contain similar to 35 mol % CH but less than 1 mol % PA, Suggesting that other anionic lipids may substitute for PA. We report that (1) phosphatidylserine (PS) and phosphatidylinositol (PI), anionic lipids that are abundant in native Torpedo membranes, also stabilize the receptor in the resting state although with reduced efficacy (similar to 50-60%) compared to PA, and (2) for nAChRs reconstituted into PA/CH membranes at different lipid-protein molar ratios, receptor functionality decreases rapidly below similar to 65 lipids per receptor. Collectively, these results are consistent with a functional requirement of a single shell lipids surrounding the nAChR and specific anionic lipid- and sterol (CH)-protein interactions.

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