scholarly journals CHEMICAL ANTAGONISM OF IONS

1928 ◽  
Vol 12 (2) ◽  
pp. 241-258 ◽  
Author(s):  
Henry S. Simms

Magnesium ions decrease the activity of divalent organic anions much more than the normal decrease produced by sodium ions. The effect is very large with short chain acids, particularly oxalic acid. The addition of sodium or potassium ions produces a marked decrease in the effect of magnesium diions on the activity of oxalate diions. Quantitative data on 0.005 molar solutions of oxalic diion over a wide range of concentrations of MgCl2 and of NaCl (or KCl) show that the following equation is obeyed: See PDF for Equation where A is an empirical value dependent on the concentration of oxalate diion (0x=). This equation has been shown to hold down to zero ionic strength of Na+ and K+, and hence to be valid in the physiological range. These observations are of biological interest since the activity of proteins should (like oxalic acid) show a similar antagonism.

2019 ◽  
Author(s):  
Susmita Ghosh ◽  
T Devanand ◽  
Upayan Baul ◽  
Satyavani Vemparala

Extensive molecular dynamics simulations have been employed to probe the effects of salts on the kinetics and dynamics of early-stage aggregated structures of steric zipper peptides in water. The simulations reveal that the chemical identity and valency of cation in the salt play a crucial roles in aggregate morphology of the peptides. Sodium ions induce the most aggregated structures but this is not replicated by potassium ions which are also monovalent. Divalent Magnesium ions induce aggregation, but to a lesser extent than that of sodium and their interactions with the charged peptides are also significantly different. The aggregate morphology in the presence of monovalent sodium ions is a compact structure with interpenetrating peptides, which differs from the more loosely connected peptides in the presence of either potassium or magnesium ions. The different ways in which the cations effectively renormalize the charges of peptides is suggested to be the cause of the differential effects of different salts studied here. These simulations underscore the importance of understanding both the valency and nature of of salts in biologically relevant aggregated structures.


2021 ◽  
Vol 22 (2) ◽  
pp. 677
Author(s):  
Tausif Altamash ◽  
Wesam Ahmed ◽  
Saad Rasool ◽  
Kabir H. Biswas

Intracellular ionic strength regulates myriad cellular processes that are fundamental to cellular survival and proliferation, including protein activity, aggregation, phase separation, and cell volume. It could be altered by changes in the activity of cellular signaling pathways, such as those that impact the activity of membrane-localized ion channels or by alterations in the microenvironmental osmolarity. Therefore, there is a demand for the development of sensitive tools for real-time monitoring of intracellular ionic strength. Here, we developed a bioluminescence-based intracellular ionic strength sensing strategy using the Nano Luciferase (NanoLuc) protein that has gained tremendous utility due to its high, long-lived bioluminescence output and thermal stability. Biochemical experiments using a recombinantly purified protein showed that NanoLuc bioluminescence is dependent on the ionic strength of the reaction buffer for a wide range of ionic strength conditions. Importantly, the decrease in the NanoLuc activity observed at higher ionic strengths could be reversed by decreasing the ionic strength of the reaction, thus making it suitable for sensing intracellular ionic strength alterations. Finally, we used an mNeonGreen–NanoLuc fusion protein to successfully monitor ionic strength alterations in a ratiometric manner through independent fluorescence and bioluminescence measurements in cell lysates and live cells. We envisage that the biosensing strategy developed here for detecting alterations in intracellular ionic strength will be applicable in a wide range of experiments, including high throughput cellular signaling, ion channel functional genomics, and drug discovery.


1961 ◽  
Vol 38 (2) ◽  
pp. 315-322
Author(s):  
J. E. TREHERNE

1. The influx of sodium and potassium ions into the central nervous system of Periplaneta americana has been studied by measuring the increase in radioactivity within the abdominal nerve cord following the injection of 24NA and 42K. into the haemolymph. 2. The calculated influx of sodium ions was approximately 320 mM./l. of nerve cord water/hr. and of potassium ions was 312 mM./l. of nerve cord water/hr. These values are very approximately equivalent to an influx per unit area of nerve cord surface of 13.9 x 10-2 M cm. -2 sec.-1 for sodium and 13.5 x 10-12 M cm. -2 sec.-1 for potassium ions. 3. The relatively rapid influxes of these ions are discussed in relation to the postulated function of the nerve sheath as a diffusion barrier. It is suggested that a dynamic steady state rather than a static impermeability must exist across the sheath surrounding the central nervous system in this insect.


1994 ◽  
Vol 03 (03) ◽  
pp. 287-298 ◽  
Author(s):  
STANLEY Y. SHAW ◽  
JAMES C. WANG

The knotting probability of a closed chain has been calculated as a function of chain dimensions and solvent properties in a number of studies. We have measured the probability of DNA knot formation upon random cyclization of linear DNA in vitro to provide an experimental test of the various theoretical treatments of the problem; parameters of these models, such as the effective chain diameter of DNA, were calculated in different concentrations of counterions. Our results in the presence of sodium ions agree well with theoretical treatments of DNA as a polyelectrolyte; knotting data in the presence of divalent magnesium ions indicate that moderate concentrations of magnesium ions can induce an attractive potential between DNA segments, resulting in negative values of the calculated effective DNA helix diameter. We discuss structures in which the divalent magnesium counterion facilitates the close apposition of two DNA segments, and review the effect of chemical- and protein-mediated crosslinks between DNA segments on DNA knot formation. Finally, we consider DNA knot formation in vivo.


Author(s):  
Majd Almakhatreh ◽  
Ezar Hafez ◽  
Ehab Tousson ◽  
Ahmed Masoud

Aims: Etoposide (Vepesid) is chemotherapeutic drugs that inhibit topoisomerase II activity and long been used for treatment of human malignancies, where it is a semi-synthetic compound derived from the plant Podophyllum peltatum. The current study was designed to investigate the possible protective effect of rosemary extract against Etoposide -induced changes in liver and kidney functions, and DNA damage in rats. Materials and Methods: A total of 50 male Wistar albino rats were divided randomly into four groups (1st group was control; 2nd group was treated with rosemary, 3rd group was received etoposide, and 4th & 5th groups was co- and post treated groups respectively). Results: The administration of Etoposide revealed a significant increase in serum ALT, AST, ALP, creatinine, urea, potassium ions, chloride ions, and DNA damage. In contrast; a significant decrease in albumen, total proteins, sodium ions, and calcium ions were when compared with control group. This increased in ALT, AST, ALP, creatinine, urea, potassium ions, chloride ions, and DNA damage was reduced after administration of rosemary when co-treated with etoposide (G4), or post-treated after etoposide  (G5) for four weeks with lowest damage in G4. Also, this decreased in albumen, total proteins, sodium ions, and calcium ions was increased after administration of rosemary when co-treated with etoposide (G4), or post-treated after etoposide (G5) for four weeks with lowest damage in G4. Conclusion: It could be concluded that rosemary has a promising role and it worth to be considered as a natural substance for protective the liver and kidney toxicity induced by etoposide (Vepesid) chemotherapy.


1958 ◽  
Vol 36 (3) ◽  
pp. 347-362 ◽  
Author(s):  
E. Riklis ◽  
J. H. Quastel

The rate of absorption of glucose from isolated surviving guinea pig intestine increases with increase of the concentration of glucose in the lumen until a maximum rate is obtained. The relation between absorption rate of glucose and initial glucose concentration conforms to an equation of the Michaelis–Menten type. The apparent Km(half saturation concentration) is 7 × 10−3M. Increase of the concentration of potassium ions in the Ringer–bicarbonate solution bathing the intestine leads to an increase of the rate of glucose absorption, this being most marked with 15.6 meq./liter K+and 14 mM glucose. No such stimulating action of potassium ions is observed on glucose absorption under anaerobic conditions. The effect of increased potassium ion concentration is to accelerate the rate of transport found with low concentrations of glucose to the maximum value found with high concentrations of the sugar. Sodium ions must be present for glucose absorption to take place and omission of magnesium ions from a Ringer–bicarbonate solution, containing 15.6 meq./liter K+, brings about a decreased rate of active glucose transport. Magnesium ions are necessary for the stimulated rate of glucose absorption obtained in the presence of potassium ions. The presence of ammonium ions decreases the rate of glucose absorption. Potassium ions may be effectively replaced by rubidium ions for stimulation of glucose transport. Cesium ions do not activate. The proportion of glucose to fructose appearing in the serosal solution, when fructose is absorbed from the mucosal solution, depends on the concentration of fructose present. The proportion may be as high as 9:1 with low (7 mM) fructose concentrations; it decreases with increasing fructose concentrations. The active transport of fructose, as demonstrated by the conversion of fructose in the isolated surviving guinea pig intestine, is enhanced by the presence of potassium ions (15.6 meq./liter). The rate of transport of fructose itself is unaffected by potassium. Using radioactive glucose and fructose, it is shown that the total amount of sugar transferred through the intestine as estimated by the radioactivity appearing in the serosal solution is approximately that calculated from chemical analyses. Potassium ions have no activating action on the transport of sugars such as sorbose, mannose, and D-glucosamine, but have a marked effect on galactose transport. The results support the conclusion that potassium ions do not influence active transport of glucose, fructose, and galactose by a change of intestinal permeability to these sugars, but do so by affecting a specific phase involved in the mechanism of active transport of sugars. The presence of L-glutamine stimulates active transport of glucose, whereas that of L-glutamate tends to diminish it.


2019 ◽  
Vol 5 (11) ◽  
pp. 1854-1866 ◽  
Author(s):  
Eva K. Stebel ◽  
Kyndal A. Pike ◽  
Huan Nguyen ◽  
Heather A. Hartmann ◽  
Mattaeus J. Klonowski ◽  
...  

Adsorbents comprising swellable organically modified silica were characterized to optimize the adsorption of a wide range of perfluoroalkyl substances from water.


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