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Published byJaqueline Hole Modified over 9 years ago
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Structural Biology of Membrane Proteins Problems of structure determination & Membrane-specific solutions KcsA structure Mechanistic insights KvAP and voltage sensing Shaker (K V 1.2)
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Key Difficulties in MP Structure Available amounts….expression systems? Solubility and solubilization; detergents Microheterogeneity; PTMs? Mutational alteration to facilitate crystallization; affinity tags Homologs; genomics
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Channel Structures Provide.. Details of structure Familial relationships Structural basis of ion selectivity Mechanism of ion dehydration by channel Linkage between pore and voltage sensor (for VS channels); gating mechanisms???
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Genomics and Channel Structures VSKC homolog (kcsA) discovered in S. lividans as ORF Monomer MW ~18kD Hydropathy analysis predicts 2 TM domains 32% identity to shaker in “signature” sequence KvAP
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What Defines a K + Channel? Founder of VS cation channel family Widely distributed in nature; multiple isoforms in most organisms Monomer MW ~70kD (eukaryotes) Activated by membrane depolarization Most isoforms have 6 predicted tm domains/monomer; functional tetramers Mutagenic analysis of pore blockers: pore between S5 and S6
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Schrempf, et al (1995) “A prokaryotic potassium ion channel with two predicted transmembrane segments from S. lividans,” EMBO J 14, 5170. Cortes & Perozo (1997) “Structural dynamics of the S. lividans K channel: oligomeric stoichiometry and stability,” Biochemistry 36, 10343. Doyle et al (1998) “The structure of the potassium channel: molecular basis of K- conduction and selectivity,” Science 280, 69. KcsA: The 1 st Structure
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VSKC Architecture?
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Sequences of K-channel Pore Regions
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Genomic Identification of KcsA Signature region
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Is KcsA a Channel? Single channel analysis Current-voltage relationship
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KcsA Oligomerizes in Detergent stain western 1. Cell extract 2. Cell super 3. Membranes 4. DDM extract 5. NTA- purified DDM extract
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KcsA Tetramers Maintained in DDM
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Structural Organization of KcsA
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KcsA Tetramer Defines Central Pore K+K+
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Polarity of KcsA Pore Region Blue, cationic; red, anionic; yellow, hydrophobic
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Aromatic Clustering at KcsA Membrane Interface
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Proposed Mechanism of Ion Translocation Lake Kalemia: note charge stabilization by helix dipoles
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Ionic Stabilization by Helix Dipole in ClC Channels
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Comparison of KcsA and ClC Pores ClC KcsA
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How Does Voltage-sensing Work? SCAM analyses consistent with transverse S4 movement
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KvAP: Structure and a Proposed Mechanism for Voltage Sensing. Jiang, MacKinnon et al (2003) “X-ray structure of a voltage-dependent K- channel,” Nature 423, 33-41; “The principle of gating charge movement in a voltage-dependent K channel,” Nature 423, 42-48. The KvAP Bombshell
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Sequence Homology in Voltage-dependent K-channels
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KvAP: a Voltage-sensitive Channel
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Backbone Structure of the KvAP Tetramer
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KvAP: The Side View Putative voltage sensor paddle
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Architecture of KvAP Monomer
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Proposed Paddle Movement during Gating
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Questions about the KvAP Structure Validity of KvAP as paradigm? Solubilization? Modification? Crystallization aids? Impact of any/all on overall structure?
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Science, 309: 897-908
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Shaker and KvAP: Not quite the Same Beast
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Accessory Subunits in K- channels
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K-channel Pores Are Conserved
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Structure of the shaker Tetramer
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Backbone Comparison: KvAP vs shaker
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Pore Communication with Voltage Sensor in Kv Channel The Kv1.2 Tetramer: note that the nearest neighbor of S4 in the red subunit is S5 from the blue subunit Closeup view showing the weak interaction between S4 and the pore region
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Revised View of Voltage-sensing Note S6 changes between open and closed states.
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