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Nat Chem Biol. 2014 Jun;10(6):457-62. doi: 10.1038/nchembio.1521. Epub 2014 Apr 28.

Cyclic dinucleotides bind the C-linker of HCN4 to control channel cAMP responsiveness.

Author information

1
1] Department of Biosciences, University of Milan, Milan, Italy. [2].
2
Department of Biosciences, University of Milan, Milan, Italy.
3
Department of Biology, Technische Universit├Ąt Darmstadt, Darmstadt, Germany.
4
School of Chemistry, University of Leeds, Leeds, UK.
5
1] Department of Biosciences, University of Milan, Milan, Italy. [2] Istituto di Biofisica, Consiglio Nazionale delle Ricerche, Milan, Italy.
6
BIOLOG Life Science Institute, Forschungslabor und Biochemica-Vertrieb GmbH D-28199, Bremen, Germany.

Erratum in

  • Nat Chem Biol. 2014 Aug;10(8):692.

Abstract

cAMP mediates autonomic regulation of heart rate by means of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, which underlie the pacemaker current If. cAMP binding to the C-terminal cyclic nucleotide binding domain enhances HCN open probability through a conformational change that reaches the pore via the C-linker. Using structural and functional analysis, we identified a binding pocket in the C-linker of HCN4. Cyclic dinucleotides, an emerging class of second messengers in mammals, bind the C-linker pocket (CLP) and antagonize cAMP regulation of the channel. Accordingly, cyclic dinucleotides prevent cAMP regulation of If in sinoatrial node myocytes, reducing heart rate by 30%. Occupancy of the CLP hence constitutes an efficient mechanism to hinder ╬▓-adrenergic stimulation on If. Our results highlight the regulative role of the C-linker and identify a potential drug target in HCN4. Furthermore, these data extend the signaling scope of cyclic dinucleotides in mammals beyond their first reported role in innate immune system.

PMID:
24776929
DOI:
10.1038/nchembio.1521
[Indexed for MEDLINE]
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