Immobilization of Lipid Substrates: Application on Phospholipase A2 Determination. Issue 12 (8th October 2015)
- Record Type:
- Journal Article
- Title:
- Immobilization of Lipid Substrates: Application on Phospholipase A2 Determination. Issue 12 (8th October 2015)
- Main Title:
- Immobilization of Lipid Substrates: Application on Phospholipase A2 Determination
- Authors:
- Karkabounas, Athanassios
Georgiadou, Dimitra G.
Argitis, Panagiotis
Psycharis, Vassilios
Nakos, George
Kosmas, Agni M.
Lekka, Marilena E. - Abstract:
- Abstract: The purpose of the study was to assess a fluorimetric assay for the determination of total phospholipase A2 (PLA2 ) activity in biological samples introducing the innovation of immobilized substrates on crosslinked polymeric membranes. The immobilized C12 ‐NBD‐PtdCho, a fluorescent analogue of phosphatidylcholine, exhibited excellent stability for 3 months at 4 °C and was not desorbed in the aqueous reaction mixture during analysis. The limit of detection was 0.5 pmol FA (0.2 pg) and the linear part of the response curve extended from 1 up to 190 nmol FA/h/mL sample. The intra‐ and inter‐day relative standard deviations (%RSD), were ≤6 and ≤9 %, respectively. Statistical comparison with other fluorescent methods showed excellent correlation and agreement. Semiempirical calculations showed a fair amount of electrostatic interaction between the NBD‐labeled substrate and the crosslinked polyvinyl alcohol with the styryl pyridinium residues (PVA‐SbQ) material, from the plane of which, the sn ‐2 acyl chain of the phospholipid stands out and is accessible by PLA2 . Atomic Force Microscopy revealed morphological alterations of the immobilized substrate after the reaction with PLA2 . Mass spectrometry showed that only C12 ‐NBD‐FA, the PLA2 hydrolysis product, was detected in the reaction mixture, indicating that PLA2 recognizes PVA‐SbQ/C12 ‐NBD‐PtdCho as a surface to perform catalysis.
- Is Part Of:
- Lipids. Volume 50:Issue 12(2015)
- Journal:
- Lipids
- Issue:
- Volume 50:Issue 12(2015)
- Issue Display:
- Volume 50, Issue 12 (2015)
- Year:
- 2015
- Volume:
- 50
- Issue:
- 12
- Issue Sort Value:
- 2015-0050-0012-0000
- Page Start:
- 1259
- Page End:
- 1271
- Publication Date:
- 2015-10-08
- Subjects:
- Phospholipases -- Phospholipase A2 -- Phospholipids -- Fluorescence -- HPLC -- Mass spectrometry
Lipids -- Periodicals
Lipids -- Periodicals
Lipiden
Lipides -- Périodiques
547.77 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0024-4201;screen=info;ECOIP ↗
http://link.springer.com/journal/11745 ↗
http://springerlink.metapress.com/content/120379/?p=67eb9addeb9a4d2a87ce760fbdd684eb&pi=0 ↗
http://www.springerlink.com/content/120379/ ↗
http://www.springer.com/gb/ ↗
http://www.aocs.org/press/ ↗ - DOI:
- 10.1007/s11745-015-4076-y ↗
- Languages:
- English
- ISSNs:
- 0024-4201
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5221.850000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5835.xml