Article abstract
Nature Structural & Molecular Biology 16, 1080 - 1085 (2009)
Published online: 27 September 2009 | doi:10.1038/nsmb.1679
Interactions between lipids and voltage sensor paddles detected with tarantula toxins
Mirela Milescu1, Frank Bosmans1,2, Seungkyu Lee3, AbdulRasheed A Alabi1,4, Jae Il Kim3 & Kenton J Swartz1
Abstract
Voltage-activated ion channels open and close in response to changes in voltage, a property that is essential for generating nerve impulses. Studies on voltage-activated potassium (Kv) channels show that voltage-sensor activation is sensitive to the composition of lipids in the surrounding membrane. Here we explore the interaction of lipids with S1–S4 voltage-sensing domains and find that the conversion of the membrane lipid sphingomyelin to ceramide-1-phosphate alters voltage-sensor activation in an S1–S4 voltage-sensing protein lacking an associated pore domain, and that the S3b–S4 paddle motif determines the effects of lipid modification on Kv channels. Using tarantula toxins that bind to paddle motifs within the membrane, we identify mutations in the paddle motif that weaken toxin binding by disrupting lipid-paddle interactions. Our results suggest that lipids bind to voltage-sensing domains and demonstrate that the pharmacological sensitivities of voltage-activated ion channels are influenced by the surrounding lipid membrane.
- Molecular Physiology and Biophysics Section, Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
- Laboratory of Toxicology, University of Leuven, Leuven, Belgium.
- Department of Life Sciences, Gwangju Institute of Science and Technology, Gwangju, Korea.
- Present address: Department of Molecular and Cellular Physiology, Stanford University, Stanford, California, USA.
Correspondence to: Mirela Milescu1 e-mail: Mirela.Milescu@nih.gov
Correspondence to: Kenton J Swartz1 e-mail: Kenton.Swartz@nih.gov
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