Two related classes of ion channels are directly regulated by cyclic nucleotide (CN) binding. The cyclic nucleotide-gated (CNG) channels are important for visual and olfactory signaling; inherited mutations in CNG channels underlie forms of retinal degeneration and color blindness. The hyperpolarization-activated, Cnmodulated (HCN) channels contribute to spontaneous firing in the brain and heart. Misregulation of HCN channels has been implicated in epilepsy, neuropathic pain, and cardiac disease. Thus, a deeper knowledge of how these channels are regulated by CNs, the focus of this proposal, is important for understanding their roles in normal neuronal function and disease. An X-ray crystal structure of a soluble C-terminal region of HCN2, including the CN-binding domain, has shown that four C-terminal regions assemble into a symmetric gating ring. However, structural and functional studies on CNG channels and functional studies of HCN2 channels indicate that subunits associate and gate as a dimer-of-dimers. The proposed studies will use several strategies to determine the nature and importance of subunit interactions in HCN and CNG gating, an unresolved issue since the studies of Hodgkin and Huxley. Mutagenesis experiments will further define the importance of specific C-terminal regions. The role of subunit interactions will be tested with tandem HCN2 tetramers in which such regions are deleted from 1,2,3 or 4 subunits. The physical proximity of neighboring HCN2 CNBDs and changes in proximity during gating will be assessed by disulfide bond formation between substituted cysteines in neighboring CNBDs. Polymer-linked CN dimers will also probe the distance between CNBDs during gating. Finally, the importance of subunit interactions in the transmembrane region will be assessed in voltage-gating of CNG channels. These studies should provide novel insights into the mechanisms of CN gating of two important classes of channels and aid in the design of therapeutic compounds to treat neurologic and cardiac diseases in which these channels participate. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
3R01NS036658-09S1
Application #
7690601
Study Section
Biophysics of Synapses, Channels, and Transporters Study Section (BSCT)
Program Officer
Silberberg, Shai D
Project Start
1998-04-01
Project End
2008-09-28
Budget Start
2007-07-01
Budget End
2008-09-28
Support Year
9
Fiscal Year
2008
Total Cost
$40,000
Indirect Cost
Name
Columbia University (N.Y.)
Department
Neurosciences
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Saponaro, Andrea; Cantini, Francesca; Porro, Alessandro et al. (2018) A synthetic peptide that prevents cAMP regulation in mammalian hyperpolarization-activated cyclic nucleotide-gated (HCN) channels. Elife 7:
Gross, Christine; Saponaro, Andrea; Santoro, Bina et al. (2018) Mechanical transduction of cytoplasmic-to-transmembrane-domain movements in a hyperpolarization-activated cyclic nucleotide-gated cation channel. J Biol Chem 293:12908-12918
Srinivas, Kalyan V; Buss, Eric W; Sun, Qian et al. (2017) The Dendrites of CA2 and CA1 Pyramidal Neurons Differentially Regulate Information Flow in the Cortico-Hippocampal Circuit. J Neurosci 37:3276-3293
Masurkar, Arjun V; Srinivas, Kalyan V; Brann, David H et al. (2017) Medial and Lateral Entorhinal Cortex Differentially Excite Deep versus Superficial CA1 Pyramidal Neurons. Cell Rep 18:148-160
Basu, Jayeeta; Zaremba, Jeffrey D; Cheung, Stephanie K et al. (2016) Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition. Science 351:aaa5694
Kupferman, Justine V; Basu, Jayeeta; Russo, Marco J et al. (2014) Reelin signaling specifies the molecular identity of the pyramidal neuron distal dendritic compartment. Cell 158:1335-1347
Saponaro, Andrea; Pauleta, Sofia R; Cantini, Francesca et al. (2014) Structural basis for the mutual antagonism of cAMP and TRIP8b in regulating HCN channel function. Proc Natl Acad Sci U S A 111:14577-82
Hu, Lei; Santoro, Bina; Saponaro, Andrea et al. (2013) Binding of the auxiliary subunit TRIP8b to HCN channels shifts the mode of action of cAMP. J Gen Physiol 142:599-612
Piskorowski, Rebecca; Santoro, Bina; Siegelbaum, Steven A (2011) TRIP8b splice forms act in concert to regulate the localization and expression of HCN1 channels in CA1 pyramidal neurons. Neuron 70:495-509
Santoro, Bina; Hu, Lei; Liu, Haiying et al. (2011) TRIP8b regulates HCN1 channel trafficking and gating through two distinct C-terminal interaction sites. J Neurosci 31:4074-86

Showing the most recent 10 out of 36 publications