Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review

Ion Channel Screening

In: Assay Guidance Manual [Internet]. Bethesda (MD): Eli Lilly & Company and the National Center for Advancing Translational Sciences; 2004.
.
Affiliations
Free Books & Documents
Review

Ion Channel Screening

Owen B McManus et al.
Free Books & Documents

Excerpt

Ion channels regulate a wide range of physiological processes including rapid electrical signaling, fluid, hormone and transmitter secretion, and proliferation. As such, ion channels are common targets for toxins and therapeutics. Ion channel screening assays have traditionally utilized indirect or low throughput approaches. Recent improvements in sensor technologies and instrumentation have provided fresh opportunities for ion channel screening that afford higher throughput, improved information content, and access to novel ion channel targets. Ion channels subtypes can display a variety of functional differences in gating and permeability mechanisms, which necessitates use of assay technologies that selected and adapted for a specific channel type. In order to successfully implement improved ion channel screening assays that provide pharmacologically relevant data, it is critical to carefully evaluate and control a variety of assay parameters. In this chapter, we provide an overview and assessment of some of the assay technologies commonly used in ion channel pharmacology and drug discovery efforts.

PubMed Disclaimer

References

    1. Anderson C.L., et al. Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism. Circulation. 2006;113(3):365–73. - PubMed
    1. Chen M.X., et al. Improved functional expression of recombinant human ether-a-go-go (hERG) K+ channels by cultivation at reduced temperature. BMC Biotechnol. 2007;7:93. - PMC - PubMed
    1. Titus S.A., et al. A new homogeneous high-throughput screening assay for profiling compound activity on the human ether-a-go-go-related gene channel. Anal Biochem. 2009;394(1):30–8. - PMC - PubMed
    1. Dunlop J., et al. High-throughput electrophysiology: an emerging paradigm for ion-channel screening and physiology. Nat Rev Drug Discov. 2008;7(4):358–68. - PubMed
    1. Clare J.J., et al. Use of planar array electrophysiology for the development of robust ion channel cell lines. Comb Chem High Throughput Screen. 2009;12(1):96–106. - PubMed

LinkOut - more resources