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  1. Artikel: LRMP inhibits cAMP potentiation of HCN4 channels by disrupting intramolecular signal transduction.

    Peters, Colin H / Singh, Rohit K / Langley, Avery A / Nichols, William G / Ferris, Hannah R / Jeffrey, Danielle A / Proenza, Catherine / Bankston, John R

    bioRxiv : the preprint server for biology

    2024  

    Abstract: Lymphoid restricted membrane protein (LRMP) is a specific regulator of the hyperpolarization-activated cyclic nucleotide-sensitive isoform 4 (HCN4) channel. LRMP prevents cAMP-dependent potentiation of HCN4 but the interaction domains, mechanisms of ... ...

    Abstract Lymphoid restricted membrane protein (LRMP) is a specific regulator of the hyperpolarization-activated cyclic nucleotide-sensitive isoform 4 (HCN4) channel. LRMP prevents cAMP-dependent potentiation of HCN4 but the interaction domains, mechanisms of action, and basis for isoform-specificity remain unknown. Here we identify the domains of LRMP essential for regulation. We show that LRMP acts by disrupting the intramolecular signal transduction between cyclic nucleotide binding and gating. And we demonstrate that multiple unique regions in HCN4 are required for LRMP isoform-specificity. Using patch clamp electrophysiology and Förster resonance energy transfer (FRET), we showed that the initial 227 residues of LRMP and the N-terminus of HCN4 are necessary for LRMP to interact with HCN4. We found that the HCN4 N-terminus and HCN4-specific residues in the C-linker are necessary for regulation of HCN4 by LRMP. And we demonstrate that LRMP-regulation can be conferred to HCN2 by addition of the HCN4 N-terminus along with mutation of 5 residues in the S5 region and C-linker to the cognate HCN4 residues. Taken together, these results suggest that LRMP inhibits HCN4 through an isoform-specific interaction involving the N-terminals of both proteins that prevents the transduction of cAMP binding into a change in channel gating via an HCN4-specific orientation of the N-terminus, C-linker, and S4-S5 linker.
    Sprache Englisch
    Erscheinungsdatum 2024-01-24
    Erscheinungsland United States
    Dokumenttyp Preprint
    DOI 10.1101/2023.08.29.555242
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: LRMP inhibits cAMP potentiation of HCN4 channels by disrupting intramolecular signal transduction.

    Peters, Colin H / Singh, Rohit K / Langley, Avery A / Nichols, William G / Ferris, Hannah R / Jeffrey, Danielle A / Proenza, Catherine / Bankston, John R

    eLife

    2024  Band 12

    Abstract: Lymphoid restricted membrane protein (LRMP) is a specific regulator of the hyperpolarization-activated cyclic nucleotide-sensitive isoform 4 (HCN4) channel. LRMP prevents cAMP-dependent potentiation of HCN4, but the interaction domains, mechanisms of ... ...

    Abstract Lymphoid restricted membrane protein (LRMP) is a specific regulator of the hyperpolarization-activated cyclic nucleotide-sensitive isoform 4 (HCN4) channel. LRMP prevents cAMP-dependent potentiation of HCN4, but the interaction domains, mechanisms of action, and basis for isoform-specificity remain unknown. Here, we identify the domains of LRMP essential for this regulation, show that LRMP acts by disrupting the intramolecular signal transduction between cyclic nucleotide binding and gating, and demonstrate that multiple unique regions in HCN4 are required for LRMP isoform-specificity. Using patch clamp electrophysiology and Förster resonance energy transfer (FRET), we identified the initial 227 residues of LRMP and the N-terminus of HCN4 as necessary for LRMP to associate with HCN4. We found that the HCN4 N-terminus and HCN4-specific residues in the C-linker are necessary for regulation of HCN4 by LRMP. Finally, we demonstrated that LRMP-regulation can be conferred to HCN2 by addition of the HCN4 N-terminus along with mutation of five residues in the S5 region and C-linker to the cognate HCN4 residues. Taken together, these results suggest that LRMP inhibits HCN4 through an isoform-specific interaction involving the N-terminals of both proteins that prevents the transduction of cAMP binding into a change in channel gating, most likely via an HCN4-specific orientation of the N-terminus, C-linker, and S4-S5 linker.
    Mesh-Begriff(e) Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels/metabolism ; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels/genetics ; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels/chemistry ; Cyclic AMP/metabolism ; Signal Transduction ; Humans ; Membrane Proteins/metabolism ; Membrane Proteins/genetics ; Animals ; Protein Binding ; HEK293 Cells ; Potassium Channels/metabolism ; Potassium Channels/genetics ; Potassium Channels/chemistry ; Patch-Clamp Techniques ; Fluorescence Resonance Energy Transfer ; Protein Isoforms/metabolism ; Protein Isoforms/genetics ; Muscle Proteins ; Receptors, Cytoplasmic and Nuclear
    Chemische Substanzen Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels ; Cyclic AMP (E0399OZS9N) ; Membrane Proteins ; PEX5L protein, human ; HCN4 protein, human ; Potassium Channels ; Protein Isoforms ; Muscle Proteins ; Receptors, Cytoplasmic and Nuclear
    Sprache Englisch
    Erscheinungsdatum 2024-04-23
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.92411
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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