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Monovalent ion traffic across the cell membrane occurs via various pathways. Evaluation of individual fluxes in whole cell is hampered by their strong interdependence. This difficulty can be overcome by computational analysis of the whole cell flux balance. However, the previous computational studies disregarded ion movement of the self-exchange type. We have taken this exchange into account. The developed software allows determination of unidirectional fluxes of all monovalent ions via the major pathways both under the balanced state and during transient processes. We show how the problem of finding the rate coefficients can be solved by measurement of monovalent ion concentrations and some of the fluxes. Interdependence of fluxes due to the mandatory conditions of electroneutrality and osmotic balance and due to specific effects can be discriminated, enabling one to identify specific changes in ion transfer machinery under varied conditions. To test the effectiveness of the developed approach we made use of the fact that Li/Na exchange is known to be an analogue of the coupled Na/Na exchange. Thus, we compared the predicted and experimental data obtained on U937 cells under varied Li+ concentrations and following inhibition of the sodium pump with ouabain. We found that the coupled Na/Na exchange in U937 cells comprises a significant portion of the entire Na+ turnover. The data showed that the loading of the sodium pump by Li/Na exchange involved in the secondary active Li+ transport at 1-10 mM external Li+ is small. This result may be extrapolated to similar Li+ and Na+ flux relationships in erythrocytes and other cells in patients treated with Li+ in therapeutic doses. The developed computational approach is applicable for studying various cells and can be useful in education for demonstrating the effects of individual transporters and channels on ion gradients, cell water content and membrane potential.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861346 | PMC |
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0153284 | PLOS |
Sci Rep
August 2025
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warszawa, Poland.
This study aims to analyze the temperature-dependent hydration of diluted ionic solutions. Three monovalent anions (Cl, Br, and I), three monovalent cations (Li, Na, and K), and one bivalent ion each (SO and Mg, respectively) were chosen as models. The partial molar volumes of all possible two-component salts (i.
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August 2025
Center for Cooperative Research on Alternative Energies (CIC EnergiGUNE), Basque Research and Technology Alliance (BRTA), Parque Tecnológico de Álava, Albert Einstein 48, 01510 Vitoria-Gasteiz, Spain.
Li and Na local ion dynamics in nitridophosphates NaV(PO)N and LiV(PO)N are evaluated here by means of solid-state nuclear magnetic resonance (NMR) and density functional theory (DFT) methods. In particular, the presence of diffusion pathways for the alkali metals within the crystal structures is evaluated experimentally by solid-state NMR and compared with bond valence energy landscape (BVEL) calculations. While no exchange between Na ions in NaV(PO)N was detected in the millisecond time scale, LiV(PO)N shows fast exchange between all Li positions in the structure.
View Article and Find Full Text PDFInorg Chem
August 2025
Instituto de Investigaciones Químicas, CSIC-Universidad de Sevilla, Av. Américo Vespucio, 49, Sevilla 41092, Spain.
The reversible storage and release of hydride equivalents remains a central challenge in the design of biomimetic redox systems. Cationic 2,6-bis(imino)pyridine organoaluminum complexes [(4-R-BIP)AlR] (where = H; ' = Me, 1a; ' = Et, 1b; = Bn; ' = Me, 1c) and their neutral 2,6-bis(imino)-4-R-dihydropyridinate counterparts [(4-R-HBIP)AlR] 2a-c are presented as chemically reversible hydride exchangers. Interconversion between these systems is achieved through strong reducing agents such as M[HBEt] (where = Li; Na) or LiAlH, while powerful electrophiles like B(CF) or cationic trityl salts PhC enable the reverse transformation, with the latter providing complete selectivity.
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July 2025
Departamento de Química e Física Molecular, Instituto de Química de São Carlos, Universidade de São Paulo, São Carlos, Brazil.
Density functional theory (DFT) is a treatment widely employed for exploring the electronic structure of atoms, molecules, solids, and complex systems. Despite its efficiency and popularity, the accuracy of DFT results is highly dependent on the choice of exchange-correlation (XC) functionals. This study evaluates several XC functionals for calculating atomization energies in 13-atom homo- and heteronuclear alkali metal clusters (X and YX, with X, Y = Li, Na, K, Rb, and Cs), comparing these results with reference data obtained from fixed-node Diffusion Monte Carlo (DMC) simulations.
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July 2025
State Key Laboratory of Advanced Fiber Materials, College of Materials Science and Engineering, Donghua University, 201620 Shanghai, P. R. China.
Metal-organic polyhedra (MOP)-based composites have emerged as promising candidates for various applications owing to their unique structure. However, the construction of strong and recyclable MOP-based composites with novel functionalities is challenging. Herein, by using telechelic aromatic polyamides as macromolecular ligands, crosslinked MOP polyamides (LODA-MOPs) were constructed coordination with copper ions (Cu).
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