Literature DB >> 23850582

Characterization of the binary mixed monolayers of α-tocopherol with phospholipids at the air-water interface.

Małgorzata Jurak1, José Miñones Conde.   

Abstract

The mixed Langmuir monolayers composed of model constituents of biological membranes, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 2-oleoyl-1-palmitoyl-sn-glycero-3-phosphocholine (POPC), and 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), were investigated to provide information on the intermolecular interactions between these membrane components and the physiologically active vitamin E-α-tocopherol (TF), as well as on the phase behavior of these mixed systems. Additionally, topography of these monolayers transferred onto the mica support was investigated by the inverted metallurgical microscope. Morphological characteristics were directly observed by Brewster angle microscopy (BAM). From the surface pressure-area isotherms and the analysis of physicochemical parameters (compressibility and mean molecular area at the maximum compressibility) it was found that depending on the acyl chains saturation degree, TF has different effect on the phospholipids. In the case of DPPC, the addition of TF to the phospholipid film causes destabilization of the ordered hydrocarbon chains, while in the POPC/DOPC-TF systems, the attractive interactions are responsible for the monolayer increased stability. Thus, the results of these studies confirm the hypothesis that α-tocopherol may play a role in the stabilization of biological membranes.
© 2013.

Entities:  

Keywords:  Brewster angle microscopy; Compression modulus; Langmuir monolayer; Phospholipids; Topography; Vitamin E

Mesh:

Substances:

Year:  2013        PMID: 23850582     DOI: 10.1016/j.bbamem.2013.07.005

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

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Journal:  PLoS One       Date:  2017-04-25       Impact factor: 3.240

3.  Effect of Ester Moiety on Structural Properties of Binary Mixed Monolayers of Alpha-Tocopherol Derivatives with DPPC.

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Journal:  Molecules       Date:  2022-07-22       Impact factor: 4.927

  3 in total

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