The broad long-term objective of this proposal is to understand the mechanisms of ion channel gating, a key molecular event that is known to regulate a variety of physiological and pathological processes. Studying the BK-type, voltage, Ca2+ and Mg2+ dependent K+ channel as a model system, the focus of this proposal is to investigate the molecular process in which voltage sensor movements, Ca2+ or Mg2+ binding are coupled to the opening of the activation gate through intramolecular interactions.
The specific aims are: I. To elucidate the role of a cytosolic domain, the AC region, in Ca2+ dependent gating. II. To investigate the interactions between the bound Mg2+ and the voltage sensor. III. To examine effects of mutations in S6 on the function of the activation gate and the sensitivity to voltage, Ca2+ and Mg2+. The role of BK channels in human health is based on their activation by voltage, Ca2+ and Mg2+, and BK channels are being pursued as a therapeutic target for various diseases. A BK channel mutation that affects voltage and Ca2+ dependent activation is linked to epilepsy and paroxysmal dyskinesia. This application seeks to dissect the molecular mechanism of BK channel gating by these stimuli, which will provide insights into BK channel related diseases and a solid basis for therapeutic developments. Several studies in recent years have provided us with X-ray crystallographic structures of potassium channels Kv1.2, KvAP, and MthK that can serve as models for BK channels. Based on these structural models and other preliminary results, a multi-disciplinary approach, including electrophysiology, mutation, chemical modification, protein biochemistry and kinetic modeling will be used to achieve the specific aims. The BK-type potassium ion channel is important for brain function and blood circulation. This research investigates the mechanism of BK channel function. The results will improve our understanding of diseases caused by the malfunction of this channel such as epilepsy and hypertension, and facilitate the development of drugs treating various diseases such as neuronal ischemia, trauma and cognitive decline. ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL070393-06A2
Application #
7316348
Study Section
Biophysics of Neural Systems Study Section (BPNS)
Program Officer
Przywara, Dennis
Project Start
2002-04-01
Project End
2011-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
6
Fiscal Year
2007
Total Cost
$373,935
Indirect Cost
Name
Washington University
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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Lee, Hsiang-Chun; Rudy, Yoram; Liang, Hongwu et al. (2017) Pro-arrhythmogenic Effects of the V141M KCNQ1 Mutation in Short QT Syndrome and Its Potential Therapeutic Targets: Insights from Modeling. J Med Biol Eng 37:780-789
Kubanek, Jan; Shi, Jingyi; Marsh, Jon et al. (2016) Ultrasound modulates ion channel currents. Sci Rep 6:24170
Cui, Jianmin (2016) Voltage-Dependent Gating: Novel Insights from KCNQ1 Channels. Biophys J 110:14-25
Hou, Panpan; Xiao, Feng; Liu, Haowen et al. (2016) Extrapolating microdomain Ca(2+) dynamics using BK channels as a Ca(2+) sensor. Sci Rep 6:17343
Varga, Zoltan; Zhu, Wandi; Schubert, Angela R et al. (2015) Direct Measurement of Cardiac Na+ Channel Conformations Reveals Molecular Pathologies of Inherited Mutations. Circ Arrhythm Electrophysiol 8:1228-39
Kasimova, Marina A; Zaydman, Mark A; Cui, Jianmin et al. (2015) PIP?-dependent coupling is prominent in Kv7.1 due to weakened interactions between S4-S5 and S6. Sci Rep 5:7474
Yang, Huanghe; Zhang, Guohui; Cui, Jianmin (2015) BK channels: multiple sensors, one activation gate. Front Physiol 6:29
Li, Min; Chang, Shan; Yang, Longjin et al. (2014) Conopeptide Vt3.1 preferentially inhibits BK potassium channels containing ?4 subunits via electrostatic interactions. J Biol Chem 289:4735-42
Zhang, Guohui; Yang, Huanghe; Liang, Hongwu et al. (2014) A charged residue in S4 regulates coupling among the activation gate, voltage, and Ca2+ sensors in BK channels. J Neurosci 34:12280-8

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