A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Plasma Protein Binding of Anisomelic Acid: Spectroscopy and Molecular Dynamic Simulations
Tekijät: Senthilkumar R, Marimuthu P, Paul P, Manojkumar Y, Arunachalam S, Eriksson JE, Johnson MS
Kustantaja: AMER CHEMICAL SOC
Julkaisuvuosi: 2016
Journal: Journal of Chemical Information and Modeling
Tietokannassa oleva lehden nimi: JOURNAL OF CHEMICAL INFORMATION AND MODELING
Lehden akronyymi: J CHEM INF MODEL
Vuosikerta: 56
Numero: 12
Aloitussivu: 2401
Lopetussivu: 2412
Sivujen määrä: 12
ISSN: 1549-9596
DOI: https://doi.org/10.1021/acs.jcim.6b00445
Tiivistelmä
Anisomelic acid (AA) is a macrocyclic cembranolide compound extracted from Anisomeles herbal, species. Recently, we have shown that AA possesses both anticancer and antiviral activity. However, to date, the plasma protein binding properties of AA are unknown. Here, we describe the molecular interactions of AA with two serum proteins, human serum albumin (HSA) and bovine serum albumin (BSA), adopting multiple physicochemical methods. Besides, molecular docking and dynamics simulations were performed to predict the interaction mode and the dynamic behavior of AA with HSA and BSA. The experimental results revealed that hydrophobic forces play a significant part in the interaction of AA to RSA and BSA. The outcomes of the principal components analysis (PCA) of the poses based on root-mean squared distances showed less variation in AA-HSA, opposed to-what is seen for BSA-AA. Furthermore, binding free energies estimated for AA-HSA and AA-BSA complexes at different temperatures (298, 303, 308, and 313 K) based on, molecular mechanics-generalised Born surface area (MMGBSA) approaches were well correlated with our experimental results.
Anisomelic acid (AA) is a macrocyclic cembranolide compound extracted from Anisomeles herbal, species. Recently, we have shown that AA possesses both anticancer and antiviral activity. However, to date, the plasma protein binding properties of AA are unknown. Here, we describe the molecular interactions of AA with two serum proteins, human serum albumin (HSA) and bovine serum albumin (BSA), adopting multiple physicochemical methods. Besides, molecular docking and dynamics simulations were performed to predict the interaction mode and the dynamic behavior of AA with HSA and BSA. The experimental results revealed that hydrophobic forces play a significant part in the interaction of AA to RSA and BSA. The outcomes of the principal components analysis (PCA) of the poses based on root-mean squared distances showed less variation in AA-HSA, opposed to-what is seen for BSA-AA. Furthermore, binding free energies estimated for AA-HSA and AA-BSA complexes at different temperatures (298, 303, 308, and 313 K) based on, molecular mechanics-generalised Born surface area (MMGBSA) approaches were well correlated with our experimental results.
Turun yliopiston Tutkimustietojärjestelmän portaali