Case Study

Functional and Pharmacological Effects of Beta Subunit Expression on BK Channels

Introducing the backbone of cellular regulation: Big Potassium (BK) channels. These gatekeepers of ion flow orchestrate many pivotal functions across diverse tissues within the human body.  

Introduction

BK channels, widely recognized as high-conductance voltage and calcium-activated potassium channels, are transmembrane proteins consisting of four pore-forming α subunits (Figure 1). Each α subunits is comprised of  seven transmembrane segments, encompassing a  voltage sensor domain and a pore-forming domain.

Schematic representation of the BK channel structure composed<br />
of the alpha and beta subunits.

Figure 1: Schematic representation of the BK channel structure composed of the alpha and beta subunits.

Far from passive entities, BK channels have a unique dual activation mechanism, responding to both membrane depolarization and intracellular calcium concentrations. This distinctive trait enables BK channels to finely  modulate cellular excitability and signalling pathways.  Activation triggers a cascade where BK channels facilitate the efflux of potassium ions, inducing membrane  hyperpolarization and effectively diminishing cellular  excitability.  Beyond their primary duty in overseeing the smooth muscle tone across vital tissues such as blood vessels, urinary blader, and the gastrointestinal tract, BK channels play a pivotal role in modulating neuronal excitability and synaptic transmission.  SB Drug Discovery have developed a suite of  comprehensive assays showcasing calcium sensitivity, kinetics, activator and inhibitor profiling, reproducibility benchmarks, and I-V assays. At SB Drug Discovery, we don’t just offer customizable assays; we provide a  pathway to novel insights, providing your research with data you can trust.  

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