Author:
del Rivero Morfin Pedro J.,Chavez Diego Scala,Jayaraman Srinidhi,Yang Lin,Kochiss Audrey L.,Colecraft Henry M.,Liu X. Shawn,Marx Steven O.,Rajadhyaksha Anjali M.,Ben-Johny Manu
Abstract
AbstractL-type Ca2+channels (CaV1.2/1.3) convey influx of calcium ions (Ca2+) that orchestrate a bevy of biological responses including muscle contraction and gene transcription. Deficits in CaV1 function play a vital role in cardiac and neurodevelopmental disorders. Yet conventional pharmacological approaches to upregulate CaV1 are limited, as excessive Ca2+influx leads to cytotoxicity. Here, we develop a genetically encoded enhancer of CaV1.2/1.3 channels (GeeC) to manipulate Ca2+entry in distinct physiological settings. Specifically, we functionalized a nanobody that targets the CaVmacromolecular complex by attaching a minimal effector domain from a CaVenhancer—leucine rich repeat containing protein 10 (Lrrc10). In cardiomyocytes, GeeC evoked a 3-fold increase in L-type current amplitude. In neurons, GeeC augmented excitation-transcription (E-T) coupling. In all, GeeC represents a powerful strategy to boost CaV1.2/1.3 function in distinct physiological settings and, in so doing, lays the groundwork to illuminate new insights on neuronal and cardiac physiology and disease.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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