Glycation Enhances Protein Association with Lipid Bilayer Membranes

Glycation is a nonenzymatic post-translational modification that leads to the formation of advanced glycation end-products (AGEs), which accumulate in the bloodstream under chronic hyperglycemia and are implicated in diabetes-related pathologies. While glycated proteins such as albumin or hemoglobin are widely used as biomarkers for glycemic control, the structural and chemical changes induced by glycation may also alter their interactions with lipid interfaces, including cellular membranes and lipoproteins, potentially affecting their biological distribution and diagnostic detectability. In this study, we investigated how glycation influences the interaction of bovine serum albumin (BSA) with supported lipid bilayers (SLBs) of different compositions, used as model systems to replicate the diversity of membrane surface charges and fluidity. Using neutron reflectometry (NR), we compared the membrane association of BSA and a chemically enhanced glycated form of BSA (gBSA), focusing on nanostructural changes at the bilayer interface. Our results showed negligible interaction of either proteins with zwitterionic or cationic membranes. In contrast, both BSA and gBSA exhibited significant binding to negatively charged bilayers, with glycation significantly amplifying this interaction. Quantitatively, the membrane-associated protein volume fraction increased from 0.11 (BSA) to 0.17 (gBSA), suggesting that glycation modifies the protein's surface properties in ways that promote stronger lipid interactions with negatively charged membranes. These findings suggest that glycation not only affects protein structure but also modulates protein-membrane affinity in a lipid-dependent manner. This has important implications for the bioavailability and behavior of glycated albumin in the bloodstream, potentially influencing the accuracy of clinical assays and contributing to membrane-related pathophysiology in diabetes. Our work highlights the need for a deeper understanding of glycation-induced changes in protein-lipid interactions and their consequences for biomarker reliability and disease mechanisms.

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Publication Details

Journal
Langmuir
Published
2025-11-12
DOI
https://doi.org/10.1021/acs.langmuir.5c03975
Citations
1
Primary Topic
Advanced Glycation End Products research
Type
article
Field-Weighted Citation Impact
1.32
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Glycation Enhances Protein Association with Lipid Bilayer Membranes

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Advanced Glycation End Products research
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article

Glycation Enhances Protein Association with Lipid Bilayer Membranes

Marco Maccarini, Donald Martin, Giovanna Fragneto, Beatrice Barletti, Isabelle Vilgrain, Jean‐Pierre Alcaraz, Nicoló Paracini, Andrew R. J. Nelson
article en
1 citations

Abstract

Glycation is a nonenzymatic post-translational modification that leads to the formation of advanced glycation end-products (AGEs), which accumulate in the bloodstream under chronic hyperglycemia and are implicated in diabetes-related pathologies. While glycated proteins such as albumin or hemoglobin are widely used as biomarkers for glycemic control, the structural and chemical changes induced by glycation may also alter their interactions with lipid interfaces, including cellular membranes and lipoproteins, potentially affecting their biological distribution and diagnostic detectability. In this study, we investigated how glycation influences the interaction of bovine serum albumin (BSA) with supported lipid bilayers (SLBs) of different compositions, used as model systems to replicate the diversity of membrane surface charges and fluidity. Using neutron reflectometry (NR), we compared the membrane association of BSA and a chemically enhanced glycated form of BSA (gBSA), focusing on nanostructural changes at the bilayer interface. Our results showed negligible interaction of either proteins with zwitterionic or cationic membranes. In contrast, both BSA and gBSA exhibited significant binding to negatively charged bilayers, with glycation significantly amplifying this interaction. Quantitatively, the membrane-associated protein volume fraction increased from 0.11 (BSA) to 0.17 (gBSA), suggesting that glycation modifies the protein's surface properties in ways that promote stronger lipid interactions with negatively charged membranes. These findings suggest that glycation not only affects protein structure but also modulates protein-membrane affinity in a lipid-dependent manner. This has important implications for the bioavailability and behavior of glycated albumin in the bloodstream, potentially influencing the accuracy of clinical assays and contributing to membrane-related pathophysiology in diabetes. Our work highlights the need for a deeper understanding of glycation-induced changes in protein-lipid interactions and their consequences for biomarker reliability and disease mechanisms.

LangmuirVol. 41(46)
Institut polytechnique de Grenoble (FR), Centre National de la Recherche Scientifique (FR), Australian Nuclear Science and Technology Organisation (AU), Inserm (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), European Spallation Source (SE), CEA Grenoble (FR), Laboratoire des Matériaux et du Génie Physique (FR), Institut Laue-Langevin (FR), Bioengineering Center (RU), Université Grenoble Alpes (FR)
Openalex Percentile: Top 14%
Advanced Glycation End Products research
1.32
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