Mechanistic insights into monomer level prevention of amyloid aggregation of lysozyme by glycyrrhizic acid

• Published in: International journal of biological macromolecules 2023-02, Vol.227, p.884-895
• Main Authors: Muthu, Shivani A., Sharma, Rahul, Qureshi, Afnaan, Parvez, Suhel, Ahmad, Basir
• Format: Article
• Language: English
• Subjects: Amyloid - chemistry; Amyloid fibrils; Amyloidogenic Proteins; Animals; Chickens - metabolism; Circular dichroism; Glycyrrhizic acid; Glycyrrhizic Acid - pharmacology; Hen egg white lysozyme; Ligand-protein interaction; Muramidase - chemistry; Solvents; Transmission electron microscopy
• ISSN: 0141-8130; 1879-0003
• DOI: 10.1016/j.ijbiomac.2022.12.166

As the primary bioactive compound of glycyrrhiza rhizome, the triterpene glycoside conjugate Glycyrrhizic acid (GA) has demonstrated neuroprotective effects in vivo. This study evaluates the effectiveness of GA as an inhibitor of GuHCl-induced amyloid aggregation of hen egg white lysozyme (HEWL). Fibril formation as measured by Thioflavin-T fluorescence, 900 light scattering, and 8-Anilinonaphthalene-1-sulfonic acid (ANS) fluorescence illustrated ∼90 % prevention of fibrils at [GA]/[HEWL] ≥2:1. Images of Transmission electron microscopy evidence for the absence of any fibril or amorphous aggregation products. The spectral characteristics of soluble HEWL were in close resemblance to unfolded monomer. Computational and fluorescence investigations performed to analyse GA-HEWL interactions demonstrated slightly higher affinity of GA to unfolded HEWL and aggregation-prone regions. The likely mechanism of monomer level aggregation prevention by GA as dermined by computational, stability, and ANS experiments illustrated that GA modulated the compactness, solvent-accessible surface, and solvent-exposed hydrophobic surfaces of aggregation-prone state of HEWL. Our findings corroborate GA as an effective inhibitor of HEWL amyloid formation. To our knowledge, GA interaction-induced inhibition of aggregation-prone states has not been previously discussed. GA's modulation of aggregation-prone states of disease-related proteins will successfully develop GA as an amyloid inhibitor for clinical trials of amyloidosis and neurodegenerative illnesses. •Glycyrrhizic acid (GA) is a molecule found inmglycyrrhiza rhizome (Mulethi) and shows neuroprotective activity.•GA binds to the monomeric aggregation precursor state of lysozyme and completely prevents its fibrillation.•GA prevents aggregation by masking the aggregation-prone surfaces.•GA may be developed into a new drug for treatment of lysozyme amyloidosis.