ArticleThe Journal of general physiology1997
Control of rectification and gating of cloned KATP channels by the Kir6.2 subunit.
Article in The Journal of general physiology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.
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.
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.
Who cites it
68 citing papers in PubMed, 134 citations in OpenAlex.
- Kir Channel Molecular Physiology, Pharmacology, and Therapeutic Implications.Handbook of experimental pharmacology · 2021Review
- Article
- Polyamines and potassium channels: A 25-year romance.The Journal of biological chemistry · 2018Review
- Anti-diabetic drug binding site in a mammalian KeLife · 2017Article
- Control of Kir channel gating by cytoplasmic domain interface interactions.The Journal of general physiology · 2017Article
- KATP Channels in the Cardiovascular System.Physiological reviews · 2016Review
- Inward rectifiers and their regulation by endogenous polyamines.Frontiers in physiology · 2014Review
- Scanning the topography of polyamine blocker binding in an inwardly rectifying potassium channel.The Journal of biological chemistry · 2013Article
- A Kir6.2 pore mutation causes inactivation of ATP-sensitive potassium channels by disrupting PIP2-dependent gating.PloS one · 2013Article
- Molecular mechanisms of chloroquine inhibition of heterologously expressed Kir6.2/SUR2A channels.Molecular pharmacology · 2012Article
- Forced gating motions by a substituted titratable side chain at the bundle crossing of a potassium channel.The Journal of biological chemistry · 2011Article
- Polyamine block of inwardly rectifying potassium channels.Methods in molecular biology (Clifton, N.J.) · 2011Article
- Article
- Fatty acid modulation and polyamine block of GluK2 kainate receptors analyzed by scanning mutagenesis.The Journal of general physiology · 2010Article
- Locale and chemistry of spermine binding in the archetypal inward rectifier Kir2.1.The Journal of general physiology · 2010Article
- Characterization and functional restoration of a potassium channel Kir6.2 pore mutation identified in congenital hyperinsulinism.The Journal of biological chemistry · 2010Article
- Voltage-dependent gating in a "voltage sensor-less" ion channel.PLoS biology · 2010Article
- Sulfonylurea receptor 1 mutations that cause opposite insulin secretion defects with chemical chaperone exposure.The Journal of biological chemistry · 2009Article
- KirBac1.1: it's an inward rectifying potassium channel.The Journal of general physiology · 2009Article
- DEND mutation in Kir6.2 (KCNJ11) reveals a flexible N-terminal region critical for ATP-sensing of the KATP channel.Biophysical journal · 2008Article
8 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
KATP channels are a functional complex of sulphonylurea receptor (SUR1, SUR2) and inward rectifier K+ (Kir6.1, Kir6.2) channel subunits. We have studied the role of the putative pore forming subunit (Kir6.2) in regulation of rectification and gating of KATP channels generated by transfection of SUR1 and Kir6.2 cDNAs in COSm6 cells. In the absence of internal polyvalent cations, the current-voltage relationship is sigmoidal. Mg2+ or spermine4+ (spm) each induces a mild inward rectification. Mutation of the asparagine at position 160 in Kir6.2 to aspartate (N160D) or glutamate (N160E) increases the degree of rectification induced by Mg2+ or spermine4+, whereas wild-type rectification is still observed after mutation to other neutral residues (alanine-N160A, glutamine-N160Q). These results are consistent with this residue lining the pore of the channel and contributing to the binding of these cations, as demonstrated for the equivalent site in homomeric ROMK1 (Kir1.1) channels. Since Kir6.2 contains no consensus ATP binding site, whereas SUR1 does, inhibition by ATP has been assumed to depend on interactions with SUR1. However, we found that the [ATP] causing half-maximal inhibition of current (Ki) was affected by mutation of N160. Channels formed from N160D or N160Q mutant subunits had lower apparent sensitivity to ATP (Ki,N160D = 46.1 microM; Ki,N160Q = 62.9 microM) than wild-type, N160E, or N160A channels (Ki = 10.4, 17.7, 6.4 microM, respectively). This might suggest that ATP binding to the channel complex was altered, although examination of channel open probabilities indicates instead that the residue at position 160 alters the ATP-independent open probability, i.e., it controls the free energy of the open state, thereby affecting the "coupling" of ATP binding to channel inhibition. The results can be interpreted in terms of a kinetic scheme whereby the residue at Kir6.2 position 160 controls the rate constants governing transitions to and from the open state, without directly affecting ATP binding or unbinding transitions.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.