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Title of Journal: J Membrane Biol

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Abbravation: The Journal of Membrane Biology

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Springer-Verlag

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DOI

10.1007/s00707-011-0477-z

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1432-1424

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The Chemical Nature of the Polar Functional Group

Authors: Subhabrata Kar Priyanka Bajaj Rajan K Tripathy Abhay H Pande
Publish Date: 2013/05/15
Volume: 246, Issue: 6, Pages: 443-452
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Abstract

Oxidative modification of phospholipids generates a variety of oxidized phospholipid OxPL species which differ considerably in their chemical compositions and molecular structures Recent results suggest that even closely related OxPL species can have considerably different biological effects However the molecular mechanism for this is not yet clear In truncated OxPLs tOxPLs the fatty acyl chain is shorter in length than the parent nonoxidized phospholipid molecules and contains a polar functional groups In a previous study we showed that two closely related tOxPL species having a similar polar functional group and differing only in the length of the oxidized fatty acyl chain exerts significantly different effects on the physicochemical properties of the nonoxidized phospholipid particles containing these lipids Kar et al Chem Phys Lipids 16454–61 2011 In this study we have characterized the effect of polar functional groups of oxidized fatty acyl chain on the physicochemical properties of the nonoxidized phospholipid particles containing these lipids Our results show that OxPL species differing only in the chemical nature of polar functional groups in their oxidized fatty acyl chain modify the properties of nonoxidized phospholipid particles containing them in a distinctive way These results indicate that different species of OxPLs induce unique changes in the physicochemical properties of lipid particles/membranes containing them and that this may lead to their different biological effects


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  1. Gating-Related Molecular Motions in the Extracellular Domain of the I Ks Channel: Implications for I Ks Channelopathy
  2. Effects of Phospholipase A 2 Inhibitors on Bilayer Lipid Membranes
  3. The Effect of Millisecond Pulsed Electric Fields (msPEF) on Intracellular Drug Transport with Negatively Charged Large Nanocarriers Made of Solid Lipid Nanoparticles (SLN): In Vitro Study
  4. Evolution of the Oligopeptide Transporter Family
  5. Slow Gating of Gap Junction Channels and Calmodulin
  6. Molecular Dynamic Simulation of Transmembrane Pore Growth
  7. Genistein Modifies the Activation Kinetics and Magnitude of Phosphorylated Wild-Type and G551D-CFTR Chloride Currents
  8. A Multi-label Classifier for Prediction Membrane Protein Functional Types in Animal
  9. Extracellular Adenine Nucleotides Regulate Na+/H+ Exchanger NHE3 Activity in A6-NHE3 Transfectants by a cAMP/PKA-dependent Mechanism
  10. Biological Properties of Melanoma and Endothelial Cells after Plasmid AMEP Gene Electrotransfer Depend on Integrin Quantity on Cells
  11. Part-2: Analytical Expressions of Concentrations of Glucose, Oxygen, and Gluconic Acid in a Composite Membrane for Closed-Loop Insulin Delivery for the Non-steady State Conditions
  12. Prediction of Protein–Protein Interaction Sites with Machine-Learning-Based Data-Cleaning and Post-Filtering Procedures
  13. Salinity-Induced Noise in Membrane Potential of Characeae Chara australis : Effect of Exogenous Melatonin
  14. Swelling-Induced Ca 2+ Influx and K + Efflux in American Alligator Erythrocytes
  15. Tubular Fluid Secretion in the Seminiferous Epithelium: Ion Transporters and Aquaporins in Sertoli Cells
  16. Ionic Currents of Human Trabecular Meshwork Cells from Control and Glaucoma Subjects
  17. Inactivation of Pseudomonas putida by Pulsed Electric Field Treatment: A Study on the Correlation of Treatment Parameters and Inactivation Efficiency in the Short-Pulse Range
  18. Effect of Chloride Channel Inhibitors on Cytosolic Ca 2+ Levels and Ca 2+ -Activated K + (Gardos) Channel Activity in Human Red Blood Cells
  19. Carbon Nanotube-Encapsulated Drug Penetration Through the Cell Membrane: An Investigation Based on Steered Molecular Dynamics Simulation
  20. Influence of Pathogenic Mutations on the Energetics of Translocon-Mediated Bilayer Integration of Transmembrane Helices
  21. Inhibition of Glial Na + and K + Currents by Tamoxifen

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