| Sodium/Hydrogen Exchanger Gene Defect in Slow-Wave Epilepsy Mutant Mice Cell, Volume 91, Issue 1, 3 October 1997, Pages 139-148 Gregory A Cox, Cathleen M Lutz, Chao-Ling Yang, Daniel Biemesderfer, Roderick T Bronson, Audrey Fu, Peter S Aronson, Jeffrey L Noebels and Wayne N Frankel Summary The “housekeeping” sodium/hydrogen exchanger, NHE1, mediates the electroneutral 1:1 exchange of Na and H across the plasma membrane. NHE1 is ubiquitous and is studied extensively for regulation of pH , cell volume, and response to growth factors. We describe a spontaneous mouse mutant, low- ave pilepsy, (), with a neurological syndrome including ataxia and a unique epilepsy phenotype consisting of 3/sec absence and tonic-clonic seizures. was fine-mapped on Chromosome 4 and identified as a null allele of . Mutants show selective neuronal death in the cerebellum and brainstem but otherwise are healthy. This first example of a disease-causing mutation in an gene provides a new tool for studying the delicate balance of neuroexcitability and cell survival within the CNS. Summary | Full Text | PDF (407 kb) |
| Binding of Cations of Group IA and IIA to Bovine Serum Amine Oxidase: Effect on the Activity Biophysical Journal, Volume 83, Issue 4, 1 October 2002, Pages 2231-2239 Maria Luisa Di Paolo, Marina Scarpa, Alessandra Corazza, Roberto Stevanato and Adelio Rigo Abstract In this paper, we report on the presence of cation binding areas on bovine serum amine oxidase, where metal ions of the groups IA and IIA, such as Na, K, Cs, Mg, and Ca, bind with various affinities. We found a cation-binding area that influences the enzyme activity if occupied, so that the catalytic reaction may be altered by some physiologically relevant cations, such as Ca and K. This binding area appears to be localized inside the enzyme active site, because some of these cations act as competitive inhibitors when highly charged amines, such as spermine and spermidine, are used as substrates. In particular, dissociation constant values () of 23 and 27mM were measured for Cs and Ca, respectively, using, as substrate, spermine, a polyamine of plasma. An additional cation-binding area, where metal ions such as Cs ( ≅ 0.1mM) and Na ( ≅ 54mM) bind without affecting the enzyme activity, was found by NMR. Abstract | Full Text | PDF (186 kb) |
| Competitive Binding of Mg, Ca, Na, and K Ions to DNA in Oriented DNA Fibers: Experimental and Monte Carlo Simulation Results Biophysical Journal, Volume 77, Issue 5, 1 November 1999, Pages 2736-2749 Nikolay Korolev, Alexander P. Lyubartsev, Allan Rupprecht and Lars Nordenskiöld Abstract Competitive binding of the most common cations of the cytoplasm (K, Na, Ca, and Mg) with DNA was studied by equilibrating oriented DNA fibers with ethanol/water solutions (65 and 52% v/v EtOH) containing different combinations and concentrations of the counterions. The affinity of DNA for the cations decreases in the order Ca>Mg≫Na≈K. The degree of Ca and/or Mg binding to DNA displays maximum changes just at physiological concentrations of salts (60–200mM) and does not depend significantly on the ethanol concentration or on the kind of univalent cation (Na or K). Ca is more tightly bound to DNA and is replaced by the monovalent cations to a lesser extent than is Mg. Similarly, Ca is a better competitor for binding to DNA than Mg: the ion exchange equilibrium constant for a 1:1 mixture of Ca and Mg ions, , changes from ≈2 in 65% EtOH (in 3–30mM NaCl and/or KCl) to ≈1.2–1.4 in 52% EtOH (in 300mM NaCl and/or KCl). DNA does not exhibit selectivity for Na or K in ethanol/water solutions either in the absence or in the presence of Ca and/or Mg. The ion exchange experimental data are compared with results of grand canonical Monte Carlo (GCMC) simulations of systems of parallel and hexagonally ordered, uniformly and discretely charged polyions with the density and spatial distribution of the charged groups modeling B DNA. A quantitative agreement with experimental data on divalent-monovalent competition has been obtained for discretely charged models of the DNA polyion (for the uniformly charged cylinder model, coincidence with experiment is qualitative). The GCMC method gives also a qualitative description of experimental results for DNA binding competitions of counterions of the same charge (Ca with Mg or K with Na). Abstract | Full Text | PDF (238 kb) |
Copyright © 1970 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 10, Issue 9, 843-858, 1 September 1970
doi:10.1016/S0006-3495(70)86339-1
Articles
Freeman W. Cope
Na+ in muscle, brain, and kidney is shown by spin-echo nuclear magnetic resonance (NMR) to consist of two fractions with different NMR parameters. The slow fraction of Na+ in these tissues has NMR relaxation times T1 and T2 of 10–15×10-3 sec, which is approximately 4–5 times shorter than for Na+ in aqueous NaCl solution. The slow fraction may represent Na+ dissolved in structured tissue water. The fast fraction of tissue Na+, which is shown to represent approximately 65% of the total tissue Na+ concentration, has T2 less than 1×10-3 sec, which resembles the values of T2 observed for Na+ complexed by synthetic ion-exchange resins. One is drawn to the conclusion that approximately 65% of total Na+ in muscle, brain, and kidney is complexed by tissue macromolecules.