Literature DB >> 14581581

Interaction mechanisms between polyamines and IRK1 inward rectifier K+ channels.

Donglin Guo1, Zhe Lu.   

Abstract

Rectification of macroscopic current through inward-rectifier K+ (Kir) channels reflects strong voltage dependence of channel block by intracellular cations such as polyamines. The voltage dependence results primarily from the movement of K+ ions across the transmembrane electric field, which accompanies the binding-unbinding of a blocker. Residues D172, E224, and E299 in IRK1 are critical for high-affinity binding of blockers. D172 appears to be located somewhat internal to the narrow K+ selectivity filter, whereas E224 and E299 form a ring at a more intracellular site. Using a series of alkyl-bis-amines of varying length as calibration, we investigated how the acidic residues in IRK1 interact with amine groups in the natural polyamines (putrescine, spermidine, and spermine) that cause rectification in cells. To block the pore, the leading amine of bis-amines of increasing length penetrates ever deeper into the pore toward D172, while the trailing amine in every bis-amine binds near a more intracellular site and interacts with E224 and E299. The leading amine in nonamethylene-bis-amine (bis-C9) makes the closest approach to D172, displacing the maximal number of K+ ions and exhibiting the strongest voltage dependence. Cells do not synthesize bis-amines longer than putrescine (bis-C4) but generate the polyamines spermidine and spermine by attaching an amino-propyl group to one or both ends of putrescine. Voltage dependence of channel block by the tetra-amine spermine is comparable to that of block by the bis-amines bis-C9 (shorter) or bis-C12 (equally long), but spermine binds to IRK1 with much higher affinity than either bis-amine does. Thus, counterintuitively, the multiple amines in spermine primarily confer the high affinity but not the strong voltage dependence of channel block. Tetravalent spermine achieves a stronger interaction with the pore by effectively behaving like a pair of tethered divalent cations, two amine groups in its leading half interacting primarily with D172, whereas the other two in the trailing half interact primarily with E224 and E299. Thus, nature has optimized not only the blocker but also, in a complementary manner, the channel for producing rapid, high-affinity, and strongly voltage-dependent channel block, giving rise to exceedingly sharp rectification.

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Year:  2003        PMID: 14581581      PMCID: PMC2229578          DOI: 10.1085/jgp.200308890

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  41 in total

1.  A modification of the Hodgkin--Huxley equations applicable to Purkinje fibre action and pace-maker potentials.

Authors:  D NOBLE
Journal:  J Physiol       Date:  1962-02       Impact factor: 5.182

2.  Mechanism of cGMP-gated channel block by intracellular polyamines.

Authors:  D Guo; Z Lu
Journal:  J Gen Physiol       Date:  2000-06       Impact factor: 4.086

3.  The structure of the potassium channel: molecular basis of K+ conduction and selectivity.

Authors:  D A Doyle; J Morais Cabral; R A Pfuetzner; A Kuo; J M Gulbis; S L Cohen; B T Chait; R MacKinnon
Journal:  Science       Date:  1998-04-03       Impact factor: 47.728

4.  Depletion of intracellular polyamines relieves inward rectification of potassium channels.

Authors:  S L Shyng; Q Sha; T Ferrigni; A N Lopatin; C G Nichols
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

5.  Regulation by spermine of native inward rectifier K+ channels in RBL-1 cells.

Authors:  L Bianchi; M L Roy; M Taglialatela; D W Lundgren; A M Brown; E Ficker
Journal:  J Biol Chem       Date:  1996-03-15       Impact factor: 5.157

6.  Tuning the voltage dependence of tetraethylammonium block with permeant ions in an inward-rectifier K+ channel.

Authors:  M Spassova; Z Lu
Journal:  J Gen Physiol       Date:  1999-09       Impact factor: 4.086

7.  Coupled ion movement underlies rectification in an inward-rectifier K+ channel.

Authors:  M Spassova; Z Lu
Journal:  J Gen Physiol       Date:  1998-08       Impact factor: 4.086

8.  Control of rectification and permeation by residues in two distinct domains in an inward rectifier K+ channel.

Authors:  J Yang; Y N Jan; L Y Jan
Journal:  Neuron       Date:  1995-05       Impact factor: 17.173

9.  Pore block versus intrinsic gating in the mechanism of inward rectification in strongly rectifying IRK1 channels.

Authors:  D Guo; Z Lu
Journal:  J Gen Physiol       Date:  2000-10       Impact factor: 4.086

10.  C-terminus determinants for Mg2+ and polyamine block of the inward rectifier K+ channel IRK1.

Authors:  M Taglialatela; E Ficker; B A Wible; A M Brown
Journal:  EMBO J       Date:  1995-11-15       Impact factor: 11.598

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  40 in total

1.  Regulation of gating by negative charges in the cytoplasmic pore in the Kir2.1 channel.

Authors:  Lai-Hua Xie; Scott A John; Bernard Ribalet; James N Weiss
Journal:  J Physiol       Date:  2004-09-30       Impact factor: 5.182

2.  Voltage profile along the permeation pathway of an open channel.

Authors:  Jorge E Contreras; Jin Chen; Albert Y Lau; Vishwanath Jogini; Benoît Roux; Miguel Holmgren
Journal:  Biophys J       Date:  2010-11-03       Impact factor: 4.033

Review 3.  Polyamines in mammalian pathophysiology.

Authors:  Francisca Sánchez-Jiménez; Miguel Ángel Medina; Lorena Villalobos-Rueda; José Luis Urdiales
Journal:  Cell Mol Life Sci       Date:  2019-06-21       Impact factor: 9.261

4.  Base of pore loop is important for rectification, activation, permeation, and block of Kir3.1/Kir3.4.

Authors:  S M Y Makary; T W Claydon; K M Dibb; M R Boyett
Journal:  Biophys J       Date:  2006-03-02       Impact factor: 4.033

5.  Functional roles of charged amino acid residues on the wall of the cytoplasmic pore of Kir2.1.

Authors:  Yuichiro Fujiwara; Yoshihiro Kubo
Journal:  J Gen Physiol       Date:  2006-03-13       Impact factor: 4.086

6.  Low-affinity spermine block mediating outward currents through Kir2.1 and Kir2.2 inward rectifier potassium channels.

Authors:  Keiko Ishihara; Ding-Hong Yan
Journal:  J Physiol       Date:  2007-07-19       Impact factor: 5.182

7.  Crystal structure of a Kir3.1-prokaryotic Kir channel chimera.

Authors:  Motohiko Nishida; Martine Cadene; Brian T Chait; Roderick MacKinnon
Journal:  EMBO J       Date:  2007-08-16       Impact factor: 11.598

8.  The cytosolic GH loop regulates the phosphatidylinositol 4,5-bisphosphate-induced gating kinetics of Kir2 channels.

Authors:  Hai-Long An; Shou-Qin Lü; Jun-Wei Li; Xuan-Yu Meng; Yong Zhan; Meng Cui; Mian Long; Hai-Lin Zhang; Diomedes E Logothetis
Journal:  J Biol Chem       Date:  2012-10-02       Impact factor: 5.157

9.  Self-assembled bifunctional surface mimics an enzymatic and templating protein for the synthesis of a metal oxide semiconductor.

Authors:  David Kisailus; Quyen Truong; Yosuke Amemiya; James C Weaver; Daniel E Morse
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-03       Impact factor: 11.205

10.  A difference in inward rectification and polyamine block and permeation between the Kir2.1 and Kir3.1/Kir3.4 K+ channels.

Authors:  Samy M Y Makary; Tom W Claydon; Decha Enkvetchakul; Colin G Nichols; Mark R Boyett
Journal:  J Physiol       Date:  2005-08-18       Impact factor: 5.182

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