Functionally-Coupled Ion Channels Begin Co-assembling at the Start of Their Synthesis
Abstract
Calcium binding to BK channels lowers their activation threshold. Hence, BK channels are functionally coupled to calcium-permeable channels. This functional coupling requires proximity of two different types of channels. Formation of an ensemble at nanometer distances between BK and CaV1.3 channels exemplifies this unique organization. We investigated the mechanism underlying their structural organization, testing the hypothesis that the assembly between BK and CaV1.3 channels is formed before their insertion at the plasma membrane. Our design used four approaches: 1) to detect the interaction between BK and CaV1.3 proteins inside the cell, 2) to identify the membranes where intracellular ensembles reside, 3) to measure the proximity between their mRNAs, and 4) to look for protein interaction at the plasma membrane soon after the start of their translation. These measures showed that a percentage of transcripts for BK and CaV1.3 channels are close and that the newly synthesized proteins interact through the endoplasmic reticulum and Golgi. Comparisons were made with other proteins and transcripts, as well as with predictions of randomized localizations of BK channels. We found evidence of assembly between BK and CaV1.3 ensembles before their insertion at the plasma membrane.
Significant statement
This work explores the proximity between the mRNAs and between newly synthesized BK and CaV1.3 channels to discover that these channels get together early in their biogenesis. Experiments employed a heterologous expression system to study the steps of protein trafficking and an insulinoma cell line of pancreatic beta cells to study proximity of endogenous channel mRNAs. The results support a new paradigm for signaling complexes, proposing that their assembly is initiated already during protein synthesis and trafficking and before insertion at their final target destination in the plasma membrane.
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