Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-13080
Neuron 1999 Apr 01;224:831-43. doi: 10.1016/s0896-6273(00)80741-2.
Show Gene links Show Anatomy links

Mutational analysis of the charge selectivity filter of the alpha7 nicotinic acetylcholine receptor.

Corringer PJ , Bertrand S , Galzi JL , Devillers-Thiéry A , Changeux JP , Bertrand D .


???displayArticle.abstract???
In the alpha7 nicotinic acetylcholine receptors, we analyze the contribution of mutations E237A and V251T, together with the proline insertion P236', in the conversion of the charge selectivity from cationic to anionic. We show that the triple mutant exhibits spontaneous openings displaying anionic selectivity. Furthermore, at position 251, hydrophilic or even negatively charged residues are compatible with an anionic channel. In contrast, the additional proline yields an anionic channel only when inserted between positions 234 and 237; insertion before 234 yields a cationic channel and after 238 alters the receptor surface expression. The coiled 234-238 loop thus directly contributes to the charge selectivity filter of the alpha7 channel.

???displayArticle.pubmedLink??? 10230802
???displayArticle.link??? Neuron