Elucidating the binding mechanism of Caralluma tuberculata metabolites with type 2 diabetes targets through molecular docking and dynamics simulations
Abstract
Introduction: Caralluma tuberculata, a medicinal plant from the Apocynaceae family, has been traditionally used to manage diabetes due to its rich secondary metabolite content.
Methodology: This study employed LC/ESI-MS/MS analysis to identify bioactive compounds in C. tuberculata, followed by in silico screening for their inhibitory effects on key carbohydrate-digesting enzymes-alpha-amylase, sucrase, and alpha-glucosidase associated with type 2 diabetes. A total of 57 compounds were evaluated through molecular docking, toxicity prediction, drug-likeness analysis, and molecular dynamics (MD) simulations.
Results: Among these, luteolin exhibited the highest binding affinities with amylase (-9.725 kcal/mol), sucrase (-8.19 kcal/mol), and alpha-glucosidase (-7.842 kcal/mol), while also demonstrating no predicted toxicity. MD simulations over 60 ns revealed stable root mean square deviation (RMSD) profiles for all protein-ligand complexes, confirming system stability. Free binding energy calculations (MM-PBSA and MM-GBSA) further suggested that luteolin had stronger, more stable interactions with amylase and sucrase compared to glucosidase.
Conclusion: This study provides a comprehensive computational evaluation of luteolin derived from Caralluma tuberculata, offering detailed insights into its enzyme-specific interactions with key carbohydrate hydrolyzing enzymes relevant to type 2 diabetes. Although the results are promising, experimental and clinical validation is essential…
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