Selective posttranslational inhibition of Ca<sub>V</sub>β<sub>1</sub>-associated voltage-dependent calcium channels with a functionalized nanobody
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Ca<sup>2+</sup> influx through high-voltage-activated calcium channels (HVACCs) controls diverse cellular functions. A critical feature enabling a singular signal, Ca<sup>2+</sup> influx, to mediate disparate functions is diversity of HVACC pore-forming α1 and auxiliary Ca<sub>V</sub>β<sub>1</sub>–Ca<sub>V</sub>β<sub>4</sub> subunits. Selective Ca<sub>V</sub>α<sub>1</sub> blockers have enabled deciphering their unique physiological roles. By contrast, the capacity to post-translationally inhibit HVACCs based on Ca<sub>V</sub>β isoform is non-existent. Conventional gene knockout/shRNA approaches do not adequately address this deficit owing to subunit reshuffling and partially overlapping functions of Ca<sub>V</sub>β isoforms. Here, we identify a nanobody (nb.E8) that selectively binds Ca<sub>V</sub>β<sub>1</sub> SH3 domain and inhibits Ca<sub>V</sub>β<sub>1</sub>-associated HVACCs by reducing channel surface density, decreasing open probability, and speeding inactivation. Functionalizing nb.E8 with Nedd4L HECT domain yielded Chisel-1 which eliminated current through Ca<sub>V</sub>β<sub>1</sub>-reconstituted Ca<sub>V</sub>1/Ca<sub>V</sub>2 and native Ca<sub>V</sub>1.1 channels in skeletal muscle, strongly suppressed depolarization-evoked Ca<sup>2+</sup> influx and excitation-transcription coupling in hippocampal neurons, but was inert against Ca<sub>V</sub>β<sub>2</sub>-associated Ca<sub>V</sub>1.2 in cardiomyocytes. The results introduce an original method for probing distinctive functions of ion channel auxiliary subunit isoforms, reveal additional dimensions of Ca<sub>V</sub>β<sub>1</sub> signaling in neurons, and describe a genetically-encoded HVACC inhibitor with unique properties.. Authors: Morgenstern, Travis J. [Columbia University Irving Medical Center, New York, NY (United States)]; Nirwan, Neha [University of California, San Francisco, CA (United States)]; Hernández-Ochoa, Erick O. [University of Maryland School of Medicine, Baltimore, MD (United States)]; Bibollet, Hugo [University of Maryland School of Medicine, Baltimore, MD (United States)] (ORCID:000000017020586X); Choudhury, Papiya [Columbia University Irving Medical Center, New York, NY (United States)]. DOE Contract: AC02-05CH11231. Subjects: 60 APPLIED LIFE SCIENCES; Calcium channels; Ion channels in the nervous system; Permeation and transport; Science & Technology - Other Topics; Ubiquitylation; X-ray crystallography
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