A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.

Current cell-based assays for determining the functional properties of high-density lipoproteins (HDL) have limitations. We report here the development of a new, robust fluorometric cell-free biochemical assay that measures HDL lipid peroxidation (HDLox) based on the oxidation of the fluorochrome Am...

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Main Authors: Theodoros Kelesidis, Christian K Roberts, Diana Huynh, Otoniel Martínez-Maza, Judith S Currier, Srinivasa T Reddy, Otto O Yang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0111716
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spelling doaj-7a035253c04b45528d912af1954e39952021-04-09T04:30:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11171610.1371/journal.pone.0111716A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.Theodoros KelesidisChristian K RobertsDiana HuynhOtoniel Martínez-MazaJudith S CurrierSrinivasa T ReddyOtto O YangCurrent cell-based assays for determining the functional properties of high-density lipoproteins (HDL) have limitations. We report here the development of a new, robust fluorometric cell-free biochemical assay that measures HDL lipid peroxidation (HDLox) based on the oxidation of the fluorochrome Amplex Red. HDLox correlated with previously validated cell-based (r = 0.47, p<0.001) and cell-free assays (r = 0.46, p<0.001). HDLox distinguished dysfunctional HDL in established animal models of atherosclerosis and Human Immunodeficiency Virus (HIV) patients. Using an immunoaffinity method for capturing HDL, we demonstrate the utility of this novel assay for measuring HDLox in a high throughput format. Furthermore, HDLox correlated significantly with measures of cardiovascular diseases including carotid intima media thickness (r = 0.35, p<0.01) and subendocardial viability ratio (r = -0.21, p = 0.05) and physiological parameters such as metabolic and anthropometric parameters (p<0.05). In conclusion, we report the development of a new fluorometric method that offers a reproducible and rapid means for determining HDL function/quality that is suitable for high throughput implementation.https://doi.org/10.1371/journal.pone.0111716
collection DOAJ
language English
format Article
sources DOAJ
author Theodoros Kelesidis
Christian K Roberts
Diana Huynh
Otoniel Martínez-Maza
Judith S Currier
Srinivasa T Reddy
Otto O Yang
spellingShingle Theodoros Kelesidis
Christian K Roberts
Diana Huynh
Otoniel Martínez-Maza
Judith S Currier
Srinivasa T Reddy
Otto O Yang
A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.
PLoS ONE
author_facet Theodoros Kelesidis
Christian K Roberts
Diana Huynh
Otoniel Martínez-Maza
Judith S Currier
Srinivasa T Reddy
Otto O Yang
author_sort Theodoros Kelesidis
title A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.
title_short A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.
title_full A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.
title_fullStr A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.
title_full_unstemmed A high throughput biochemical fluorometric method for measuring lipid peroxidation in HDL.
title_sort high throughput biochemical fluorometric method for measuring lipid peroxidation in hdl.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Current cell-based assays for determining the functional properties of high-density lipoproteins (HDL) have limitations. We report here the development of a new, robust fluorometric cell-free biochemical assay that measures HDL lipid peroxidation (HDLox) based on the oxidation of the fluorochrome Amplex Red. HDLox correlated with previously validated cell-based (r = 0.47, p<0.001) and cell-free assays (r = 0.46, p<0.001). HDLox distinguished dysfunctional HDL in established animal models of atherosclerosis and Human Immunodeficiency Virus (HIV) patients. Using an immunoaffinity method for capturing HDL, we demonstrate the utility of this novel assay for measuring HDLox in a high throughput format. Furthermore, HDLox correlated significantly with measures of cardiovascular diseases including carotid intima media thickness (r = 0.35, p<0.01) and subendocardial viability ratio (r = -0.21, p = 0.05) and physiological parameters such as metabolic and anthropometric parameters (p<0.05). In conclusion, we report the development of a new fluorometric method that offers a reproducible and rapid means for determining HDL function/quality that is suitable for high throughput implementation.
url https://doi.org/10.1371/journal.pone.0111716
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