Evidence map›Paper›PMID 19113860›Full record

ReviewBiochemistry2009

Chemical tools for K(+) channel biology.

Christopher A Ahern, William R Kobertz

Open access · greenAbstract readReview
In one paragraph

Review in Biochemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. The Concise Guide to PHARMACOLOGY 2013/14: ion channels.British journal of pharmacology · 2013
    Article
  3. Article
  4. Review
  5. Chemical control of metabolically-engineered voltage-gated K+ channels.Bioorganic & medicinal chemistry letters · 2011
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Christopher A AhernDepartment of Anesthesiology, University of British Columbia, 2350 Health Science Mall, Vancouver, BC V6T 1Z3, Canada. cahern@interchange.ubc.ca
William R Kobertz
University of British Columbia · CAUniversity of Massachusetts Chan Medical School · US

Funding

K+ channel complexes: assembly, trafficking and functionR01GM070650 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KOBERTZ, WILLIAM R · 2005 to 2022
$5.7M
K+ channel protein complexes in auditory biologyR01DC007669 · NIDCD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KOBERTZ, WILLIAM R · 2005 to 2009
$2.1M
NIDCD NIH HHS DC-007669NIDCD NIH HHS R01 DC007669NIGMS NIH HHS GM-070650NIGMS NIH HHS R01 GM070650
6 · The paper itself

Abstract

K(+) channels are revered for their universal action of suppressing electrical activity in nerve and muscle, as well as regulating salt and water transport in epithelial tissues involved in metabolism and digestion. These multisubunit membrane-embedded proteins carry out their physiological chore, selectively allowing the passage of potassium across the membrane, in response to changes in membrane voltage and ligand concentration. Elucidating the diverse gating properties of K(+) channels is of great biological interest since their molecular motions provide insight into how these structurally similar proteins function in a wide variety of tissues. Armed with patch clamps, chart recorders, and now high-resolution structures, electrophysiologists have been dipping into the top tray of the chemist's tool box: synthesizing cysteine-modifying agents and organic cations and grinding up insects, spiders, and other vermin to isolate natural products to poke, probe, and prod K(+) channels. Recently, there has been further cross-fertilization between chemists and K(+) channelologists, resulting in greater accessibility to more elaborate synthetic methodologies and screening approaches. In this review, we catalogue the evolution of chemical tools and approaches that have been utilized to elucidate the mechanistic underpinnings of K(+) channel biology.

Indexed as

Amino AcidsHumansPotassium Channel BlockersPotassium ChannelsProtein SubunitsQuaternary Ammonium CompoundsSmall Molecule LibrariesAmino AcidsPotassium Channel BlockersPotassium ChannelsProtein SubunitsQuaternary Ammonium CompoundsSmall Molecule Libraries

Identifiers

PMID19113860
PMCPMC2629505
OpenAlexW2059840091

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.