Literature DB >> 2589516

Kinetics of ATP-sensitive K+ channel revealed with oil-gate concentration jump method.

D Y Qin1, M Takano, A Noma.   

Abstract

Kinetics for gating the ATP-sensitive K+ channel was studied by exposing the inside-out patch to instantaneous changes in the intracellular concentration of ATP ( [ATP]i) using the oil-gate concentration jump technique in guinea pig ventricular cells. The closing time course of the channel after increasing [ATP]i was exponential with a time constant (tau), which decreased with increasing [ATP]i. The linear 1/tau - [ATP]i relation revealed two different binding (closing) rate constants (mu) of 51.7 and 5.6 mM-1.s-1 and predicted a common unbinding (opening) rate constant (lambda) of 3.2 s-1. A variable latent period was observed before channel opening when [ATP]i was decreased. The mechanism of latency is not clear. Once the channel started to open at the change lowering [ATP]i, the opening time course was exponential. Measurements of the exponential tau obtained at 0 mM [ATP]i were divided into two groups with corresponding lambda of 2.8 and 20.1 s-1, respectively. The former agrees with the predicted value of 3.2 s-1, but in the latter case, tau for opening increased as [ATP]i was increased. This increase in tau was attributed to a decrease of lambda, which approached an asymptotic value of 3.2 s-1. We conclude that binding and unbinding of one molecule of ATP determine the gating of ATP-sensitive K+ channel. Different pairs of mu and lambda result in four types of gating patterns and practically two states of sensitivities to ATP.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2589516     DOI: 10.1152/ajpheart.1989.257.5.H1624

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  28 in total

1.  The kinetic and physical basis of K(ATP) channel gating: toward a unified molecular understanding.

Authors:  D Enkvetchakul; G Loussouarn; E Makhina; S L Shyng; C G Nichols
Journal:  Biophys J       Date:  2000-05       Impact factor: 4.033

2.  The I182 region of k(ir)6.2 is closely associated with ligand binding in K(ATP) channel inhibition by ATP.

Authors:  L Li; J Wang; P Drain
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

3.  Concerted gating mechanism underlying KATP channel inhibition by ATP.

Authors:  Peter Drain; Xuehui Geng; Lehong Li
Journal:  Biophys J       Date:  2004-04       Impact factor: 4.033

4.  The effect of intracellular pH on ATP-dependent potassium channels of frog skeletal muscle.

Authors:  N W Davies; N B Standen; P R Stanfield
Journal:  J Physiol       Date:  1992-01       Impact factor: 5.182

5.  Multiple actions of pinacidil on adenosine triphosphate-sensitive potassium channels in guinea-pig ventricular myocytes.

Authors:  Z Fan; K Nakayama; M Hiraoka
Journal:  J Physiol       Date:  1990-11       Impact factor: 5.182

Review 6.  ATP-dependent potassium channels of muscle cells: their properties, regulation, and possible functions.

Authors:  N W Davis; N B Standen; P R Stanfield
Journal:  J Bioenerg Biomembr       Date:  1991-08       Impact factor: 2.945

7.  KATP channel inhibition by ATP requires distinct functional domains of the cytoplasmic C terminus of the pore-forming subunit.

Authors:  P Drain; L Li; J Wang
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

8.  Control of rectification and gating of cloned KATP channels by the Kir6.2 subunit.

Authors:  S Shyng; T Ferrigni; C G Nichols
Journal:  J Gen Physiol       Date:  1997-08       Impact factor: 4.086

9.  Intracellular nucleotide-mediated gating of SUR/Kir6.0 complex potassium channels expressed in a mammalian cell line and its modification by pinacidil.

Authors:  E Satoh; M Yamada; C Kondo; V P Repunte; Y Horio; T Iijima; Y Kurachi
Journal:  J Physiol       Date:  1998-09-15       Impact factor: 5.182

10.  Cytoplasmic acidosis induces multiple conductance states in ATP-sensitive potassium channels of cardiac myocytes.

Authors:  Z Fan; T Furukawa; T Sawanobori; J C Makielski; M Hiraoka
Journal:  J Membr Biol       Date:  1993-11       Impact factor: 1.843

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.