Author

C. Proenza

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Physiology· 3 Biophysics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 4 Assay:electrophysiology· 3 Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:cell type annotation· 1 Approach:machine learning (classical)· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

C. H. Peters· 4 shared E. Grandi· 2 shared J. R. Bankston· 2 shared S. Morotti· 2 shared A. A. Langley· 1 shared B. P. Bean· 1 shared C. Haimbaugh· 1 shared C. Rickert· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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4 shared papersPhysiology

C. H. Peters

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Author profile →

4 papers

Recent·Most cited

LRMP inhibits the cAMP potentiation of HCN4 channels by disrupting intramolecular signal transduction

J. R. Bankston, C. Proenza, C. H. Peters, R. K. Singh, A. A. Langley, W. G. Nichols, H. R. Ferris, D. A. Jeffrey

This study identifies how LRMP inhibits cAMP-induced potentiation of HCN4 channels by disrupting intramolecular signaling, revealing isoform-specific interaction domains.

bioRxiv · Aug 29, 2023Biophysics

The funny current If is essential for the fight-or-flight response in cardiac pacemaker cells

C. H. Peters, C. Rickert, S. Morotti, E. Grandi, C. Proenza

This study identifies the role of the funny current If in mediating the fight-or-flight response in cardiac pacemaker cells using machine learning and dynamic clamp experiments.

bioRxiv · May 7, 2022Physiology

Bi-directional flow of the funny current (If) during the pacemaking cycle in murine sinoatrial node myocytes

C. H. Peters, P. Liu, S. Morotti, S. C. Gantz, E. Grandi, B. P. Bean, C. Proenza

This study quantifies the funny current (If) in murine sinoatrial node myocytes, showing its persistent activity and dual role in driving membrane potential oscillations during pacemaking.

bioRxiv · Mar 10, 2021Physiology

Isoform-specific regulation of HCN4 channels by a family of endoplasmic reticulum proteins

C. H. Peters, M. E. Myers, J. Juchno, C. Haimbaugh, H. Bichraoui, Y. Du, J. R. Bankston, L. A. Walker, C. Proenza

This paper identifies two ER proteins, LRMP and IRAG, that modulate HCN4 channel function differently, with LRMP inhibiting and IRAG enhancing HCN4 activity in a cAMP-independent manner.

bioRxiv · Apr 10, 2020Physiology