Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8835
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dc.contributor.authorKanwa, Nishuen_US
dc.contributor.authorDe, Soumya Kantien_US
dc.contributor.authorMaity, Avijiten_US
dc.contributor.authorChakraborty, Anjanen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:29:58Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:29:58Z-
dc.date.issued2020-
dc.identifier.citationKanwa, N., De, S. K., Maity, A., & Chakraborty, A. (2020). Interaction of aliphatic amino acids with zwitterionic and charged lipid membranes: Hydration and dehydration phenomena. Physical Chemistry Chemical Physics, 22(6), 3234-3244. doi:10.1039/c9cp06188fen_US
dc.identifier.issn1463-9076-
dc.identifier.otherEID(2-s2.0-85079330965)-
dc.identifier.urihttps://doi.org/10.1039/c9cp06188f-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/8835-
dc.description.abstractIn the present contribution, we investigate the interactions of lipid bilayer membranes of different charges and different phase states with aliphatic amino acids of varying charge (aspartic acid, glutamic acid, arginine and lysine) and hydrophobicity (serine, leucine and valine) by steady state and time-resolved spectroscopic techniques, dynamic light scattering (DLS) measurements and confocal imaging (CLSM). The study reveals that negatively charged amino acids such as aspartic acid and glutamic acid interact strongly with the lipid membranes particularly with negatively charged lipid membranes by stabilizing their gel phase. On the other hand, positively charged amino acids bring in hydration in the membranes. We explain this unique observation by the shift in pKa of amino acids in the vicinity of the lipid membranes and solvation and desolvation processes in the light of recent computer simulations. We also find that hydrogen bonding plays a significant role in governing the interaction of aliphatic amino acids with zwitterionic lipid membranes. The more polar serine bearing a hydroxyl group at the terminal carbon offers a stronger interaction with the lipid bilayer membranes as compared to its analogues leucine and valine, which are hydrophobic in nature. This journal is © the Owner Societies.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourcePhysical Chemistry Chemical Physicsen_US
dc.subjectamino aciden_US
dc.subjectionen_US
dc.subjectchemical phenomenaen_US
dc.subjectchemical structureen_US
dc.subjectchemistryen_US
dc.subjectcomputer simulationen_US
dc.subjectdehydrationen_US
dc.subjecthydrogen bonden_US
dc.subjectkineticsen_US
dc.subjectlipid bilayeren_US
dc.subjectmolecular modelen_US
dc.subjectstructure activity relationen_US
dc.subjectAmino Acidsen_US
dc.subjectComputer Simulationen_US
dc.subjectDehydrationen_US
dc.subjectHydrogen Bondingen_US
dc.subjectHydrophobic and Hydrophilic Interactionsen_US
dc.subjectIonsen_US
dc.subjectKineticsen_US
dc.subjectLipid Bilayersen_US
dc.subjectModels, Molecularen_US
dc.subjectMolecular Structureen_US
dc.subjectStructure-Activity Relationshipen_US
dc.titleInteraction of aliphatic amino acids with zwitterionic and charged lipid membranes: Hydration and dehydration phenomenaen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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