Biochemical and Functional Characterization of Charge-Defined Subfractions of High-Density Lipoprotein From Normal Adults

• Published in: Analytical chemistry (Washington) Vol. 85; no. 23; pp. 11440 - 11448
• Main Authors: Hsieh, Ju-Yi, Chang, Chiz-Tzung, Huang, Max T, Chang, Chia-Ming, Chen, Chia-Ying, Shen, Ming-Yi, Liao, Hsin-Yi, Wang, Guei-Jane, Chen, Chu-Huang, Chen, Chao-Jung, Yang, Chao-Yuh
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 03.12.2013
• Subjects: Adult; Anion Exchange Resins - chemistry; Antioxidants; Chemical Fractionation - methods; Cholesterol; Chromatography; Comparative analysis; Desorption; Efflux; Female; High density; Humans; Lipoproteins; Lipoproteins, HDL - analysis; Lipoproteins, HDL - chemistry; Male; Mass spectrometry; Middle Aged; Proteins
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac402516u

High-density lipoprotein (HDL) is regarded as atheroprotective because it provides antioxidant and anti-inflammatory benefits and plays an important role in reverse cholesterol transport. In this paper, we outline a novel methodology for studying the heterogeneity of HDL. Using anion-exchange chromatography, we separated HDL from 6 healthy individuals into five subfractions (H1 through H5) with increasing charge and evaluated the composition and biologic activities of each subfraction. Sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis showed that apolipoprotein (apo) AI and apoAII were present in all 5 subfractions; apoCI was present only in H1, and apoCIII and apoE were most abundantly present in H4 and H5. HDL-associated antioxidant enzymes such as lecithin-cholesterol acyltransferase, lipoprotein-associated phospholipase A2, and paraoxonase 1 were most abundant in H4 and H5. Lipoprotein isoforms were analyzed in each subfraction by using matrix-assisted laser desorption-time-of-flight mass spectrometry. To quantify other proteins in the HDL subfractions, we used the isobaric tags for the relative and absolute quantitation approach followed by nanoflow liquid chromatography–tandem mass spectrometry analysis. Most antioxidant proteins detected were found in H4 and H5. The ability of each subfraction to induce cholesterol efflux from macrophages increased with increasing HDL electronegativity, with the exception of H5, which promoted the least efflux activity. In conclusion, anion-exchange chromatography is an attractive method for separating HDL into subfractions with distinct lipoprotein compositions and biologic activities. By comparing the properties of these subfractions, it may be possible to uncover HDL-specific proteins that play a role in disease.