Clustering and Coupled Gating Modulate the Activity in KcsA, a Potassium Channel Model

• Published in: The Journal of biological chemistry 2006-07, Vol.281 (27), p.18837-18848
• Main Authors: Molina, Maria L., Barrera, Francisco N., Fernández, Asia M., Poveda, Jose A., Renart, Maria L., Encinar, Jose A., Riquelme, Gloria, González-Ros, Jose M.
• Format: Article
• Language: English
• Subjects: Bacterial Proteins - chemistry; Bacterial Proteins - metabolism; Cell Membrane - chemistry; Cell Membrane - metabolism; Cell Membrane - ultrastructure; Ion Channel Gating; Liposomes; Microscopy, Confocal; Models, Biological; Patch-Clamp Techniques; Potassium Channels - chemistry; Potassium Channels - metabolism; Streptomyces lividans
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M600342200

Different patterns of channel activity have been detected by patch clamping excised membrane patches from reconstituted giant liposomes containing purified KcsA, a potassium channel from prokaryotes. The more frequent pattern has a characteristic low channel opening probability and exhibits many other features reported for KcsA reconstituted into planar lipid bilayers, including a moderate voltage dependence, blockade by Na+, and a strict dependence on acidic pH for channel opening. The predominant gating event in this low channel opening probability pattern corresponds to the positive coupling of two KcsA channels. However, other activity patterns have been detected as well, which are characterized by a high channel opening probability (HOP patterns), positive coupling of mostly five concerted channels, and profound changes in other KcsA features, including a different voltage dependence, channel opening at neutral pH, and lack of Na+ blockade. The above functional diversity occurs correlatively to the heterogeneous supramolecular assembly of KcsA into clusters. Clustering of KcsA depends on protein concentration and occurs both in detergent solution and more markedly in reconstituted membranes, including giant liposomes, where some of the clusters are large enough (up to micrometer size) to be observed by confocal microscopy. As in the allosteric conformational spread responses observed in receptor clustering (Bray, D. and Duke, T. (2004) Annu. Rev. Biophys. Biomol. Struct. 33, 53-73) our tenet is that physical clustering of KcsA channels is behind the observed multiple coupled gating and diverse functional responses.