Cytotoxicity and comparative binding mechanism of piperine with human serum albumin and α-1-acid glycoprotein

Abstract

Human serum albumin (HSA) and α-1-acid glycoprotein (AGP) (acute phase protein) are the plasma proteins in blood system which transports many drugs. To understand the pharmacological importance of piperine molecule, here, we studied the anti-inflammatory activity of piperine on mouse macrophages (RAW 264.7) cell lines, which reveals that piperine caused an increase in inhibition growth of inflammated macrophages. Further, the fluorescence maximum quenching of proteins were observed upon binding of piperine to HSA and AGP through a static quenching mechanism. The binding constants obtained from fluorescence emission were found to be K_piperine= 5.7 ± .2 × 10⁵ M⁻¹ and K_piperine = 9.3± .25 × 10⁴ M⁻¹ which correspond to the free energy of −7.8 and −6.71 kcal M⁻¹at 25 °C for HSA and AGP, respectively. Further, circular dichrosim studies revealed that there is a marginal change in the secondary structural content of HSA due to partial destabilization of HSA–piperine complexes. Consequently, inference drawn from the site-specific markers (phenylbutazone, site I marker) studies to identify the binding site of HSA noticed that piperine binds at site I (IIA), which was further authenticated by molecular docking and molecular dynamic (MD) studies. The binding constants and free energy corresponding to experimental and computational analysis suggest that there are hydrophobic and hydrophilic interactions when piperine binds to HSA. Additionally, the MD studies have showed that HSA–piperine complex reaches equilibration state at around 3 ns, which prove that the HSA–piperine complex is stable in nature.

Keywords:

• cytotoxicity
• drug binding
• fluorescence quenching
• α-1-acid glycoprotein
• human serum albumin
• molecular dynamics simulation
• piperine

Acknowledgments

MK acknowledges UGC-New Delhi for providing financial support under the scheme of Dr. D. S. Kothari Postdoctoral Fellowship. We thank CIL and BIF, University of Hyderabad, for CD and Bioinformatics facilities.

Additional information

Funding

Funding. This work was supported by Department of Science and Technology [grant number SR/SO/BB-0123/2010 and DST-FIST], DBT-CREBB, India and UPE-2, University of Hyderabad.