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Biochemical and computational insights of adenosine deaminase inhibition by Epigallocatechin gallate
Institution:1. Department of Obstetrics and Gynecology, The C.S. Mott Center for Human Growth and Development, Detroit, MI 48201, USA;2. Department of Biochemistry and Genetics, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus 7, Palestine;3. Department of Microbiology, Immunology and Biochemistry, Wayne State University School of Medicine, Detroit, MI, 48201, USA
Abstract:Epigallocatechin gallate, a flavonoid from Camellia sinensis possess various pharmacological activities such as anticancer, antimicrobial and antioxidant etc. Adenosine deaminase, (ADA), is a key enzyme involved in the purine metabolism, the inhibitors of which is being considered as highly promising candidate for the development of anti-proliferative and anti-inflammatory drugs. In this work we studied adenosine deaminase inhibitory activity of epigallocatechin gallate by using biophysical and computational methods. The enzyme inhibition study result indicated that epigallocatechin gallate possess strong inhibitory activity on ADA. ITC study revealed the energetics of binding. Also the binding is confirmed by using fluorescence spectroscopy. The structural details of binding are obtained from molecular docking and MD simulation studies.
Keywords:Adenosine deaminase  Epigallocatechin gallate  ITC  Fluorescence spectroscopy  Molecular dynamics
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