Quantitative glycoproteomics of high-density lipoproteins

Tang, Xinyu; Wong, Maurice; Tena, J. L. Ruiz; Zhu, Chenghao; Rhodes, Christopher; Zhou, Qingwen; Vinjamuri, Anita; Oloumi, Armin; Boddu, Sucharita; Luxardi, Guillaume; Maverakis, Emanual; Lebrilla, Carlito B.; Zivkovic, Angela M.

doi:10.1039/d2ra02294j

Cited by 1 publication

(1 citation statement)

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“…Sialidase specifically removes terminal sialic acid residues from glycan chains. Without sialic acids, proteins of HDL particles that are known to be sialylated (e.g., apoA-II, apoCs, apoD, apoE, apoJ, and apoM) [64] may adopt different conformations, affecting the structure and function of HDL particles.…”

Section: Discussionmentioning

confidence: 99%

Lutein and Zeaxanthin Enhance, Whereas Oxidation, Fructosylation, and Low pH Damage High-Density Lipoprotein Biological Functionality

Zheng,

Hong,

Agus

et al. 2024

Antioxidants

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High-density lipoproteins (HDLs) are key regulators of cellular cholesterol homeostasis but are functionally altered in many chronic diseases. The factors that cause HDL functional loss in chronic disease are not fully understood. It is also unknown what roles antioxidant carotenoids play in protecting HDL against functional loss. The aim of this study was to measure how various disease-associated chemical factors including exposure to (1) Cu2+ ions, (2) hypochlorous acid (HOCL), (3) hydrogen peroxide (H2O2), (4) sialidase, (5) glycosidase, (6) high glucose, (7) high fructose, and (8) acidic pH, and the carotenoid antioxidants (9) lutein and (10) zeaxanthin affect HDL functionality. We hypothesized that some of the modifications would have stronger impacts on HDL particle structure and function than others and that lutein and zeaxanthin would improve HDL function. HDL samples were isolated from generally healthy human plasma and incubated with the corresponding treatments listed above. Cholesterol efflux capacity (CEC), lecithin–cholesterol acyl transferase (LCAT) activity, and paraoxonase-1 (PON1) activity were measured in order to determine changes in HDL functionality. Median HDL particle diameter was increased by acidic pH treatment and reduced by HOCl, high glucose, high fructose, N-glycosidase, and lutein treatments. Acidic pH, oxidation, and fructosylation all reduced HDL CEC, whereas lutein, zeaxanthin, and sialidase treatment improved HDL CEC. LCAT activity was reduced by acidic pH, oxidation, high fructose treatments, and lutein. PON1 activity was reduced by sialidase, glycosidase, H2O2, and fructose and improved by zeaxanthin and lutein treatment. These results show that exposure to oxidizing agents, high fructose, and low pH directly impairs HDL functionality related to cholesterol efflux and particle maturation, whereas deglycosylation impairs HDL antioxidant capacity. On the other hand, the antioxidants lutein and zeaxanthin improve or preserve both HDL cholesterol efflux and antioxidant activity but have no effect on particle maturation.

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Section: Discussionmentioning

confidence: 99%