Literature DB >> 24463792

Multi-ion versus single-ion conduction mechanisms can yield current rectification in biological ion channels.

Tamsyn A Hilder1, Ben Corry, Shin-Ho Chung.   

Abstract

There is clear evidence that the net magnitude of negative charge at the intracellular end of inwardly rectifying potassium channels helps to generate an asymmetry in the magnitude of the current that will pass in each direction. However, a complete understanding of the physical mechanism that links these charges to current rectification has yet to be obtained. Using Brownian dynamics, we compare the conduction mechanism and binding sites in rectifying and non-rectifying channel models. We find that in our models, rectification is a consequence of asymmetry in the hydrophobicity and charge of the pore lining. As a consequence, inward conduction can occur by a multi-ion conduction mechanism. However, outward conduction is restricted, since there are fewer ions at the intracellular entrance and outwardly moving ions must cross the pore on their own. We pose the question as to whether the same mechanism could be at play in inwardly rectifying potassium channels.

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Year:  2014        PMID: 24463792      PMCID: PMC4049380          DOI: 10.1007/s10867-013-9338-4

Source DB:  PubMed          Journal:  J Biol Phys        ISSN: 0092-0606            Impact factor:   1.365


  33 in total

1.  Modeling diverse range of potassium channels with Brownian dynamics.

Authors:  Shin-Ho Chung; Toby W Allen; Serdar Kuyucak
Journal:  Biophys J       Date:  2002-07       Impact factor: 4.033

2.  Structural basis of inward rectification: cytoplasmic pore of the G protein-gated inward rectifier GIRK1 at 1.8 A resolution.

Authors:  Motohiko Nishida; Roderick MacKinnon
Journal:  Cell       Date:  2002-12-27       Impact factor: 41.582

3.  A ring of eight conserved negatively charged amino acids doubles the conductance of BK channels and prevents inward rectification.

Authors:  Tinatin I Brelidze; Xiaowei Niu; Karl L Magleby
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-03       Impact factor: 11.205

4.  Ohmic conductance through the inwardly rectifying K channel and blocking by internal Mg2+.

Authors:  H Matsuda; A Saigusa; H Irisawa
Journal:  Nature       Date:  1987 Jan 8-14       Impact factor: 49.962

5.  Conduction and block of inward rectifier K+ channels: predicted structure of a potent blocker of Kir2.1.

Authors:  Tamsyn A Hilder; Shin-Ho Chung
Journal:  Biochemistry       Date:  2013-01-23       Impact factor: 3.162

Review 6.  Kir channels in the CNS: emerging new roles and implications for neurological diseases.

Authors:  C Neusch; J H Weishaupt; M Bähr
Journal:  Cell Tissue Res       Date:  2003-02-04       Impact factor: 5.249

7.  Mechanism of rectification in inward-rectifier K+ channels.

Authors:  Donglin Guo; Yajamana Ramu; Angela M Klem; Zhe Lu
Journal:  J Gen Physiol       Date:  2003-03-17       Impact factor: 4.086

8.  IRK1 inward rectifier K(+) channels exhibit no intrinsic rectification.

Authors:  Donglin Guo; Zhe Lu
Journal:  J Gen Physiol       Date:  2002-10       Impact factor: 4.086

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

Authors:  Donglin Guo; Zhe Lu
Journal:  J Gen Physiol       Date:  2003-11       Impact factor: 4.086

10.  Intrinsic gating of inward rectifier in bovine pulmonary artery endothelial cells in the presence or absence of internal Mg2+.

Authors:  M R Silver; T E DeCoursey
Journal:  J Gen Physiol       Date:  1990-07       Impact factor: 4.086

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