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Inhibition of pro-/active MMP-2 by green tea catechins and prediction of their interaction by molecular docking studies.
- Source :
-
Molecular and cellular biochemistry [Mol Cell Biochem] 2017 Mar; Vol. 427 (1-2), pp. 111-122. Date of Electronic Publication: 2016 Dec 24. - Publication Year :
- 2017
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Abstract
- Matrix metalloproteinases (MMPs) play a crucial role in developing different types of lung diseases, e.g., pulmonary arterial hypertension (PAH). Green tea polyphenolic catechins such as EGCG and ECG have been shown to ameliorate various types of diseases including PAH. Our present study revealed that among the four green tea catechins (EGCG, ECG, EC, and EGC), EGCG and ECG inhibit pro-/active MMP-2 activities in pulmonary artery smooth muscle cell (PASMC) culture supernatant. Based on the above, we investigated the interactions of pro-/active MMP-2 with the green tea catechins by computational methods. In silico analysis revealed a strong interaction of pro-/active MMP-2 with EGCG/ECG, and galloyl group has been observed to be responsible for this interaction. The in silico analysis corroborated our experimental observation that EGCG and ECG are active in preventing both the proMMP-2 and MMP-2 activities. Importantly, these two catechins appeared to be better inhibitors for proMMP-2 in comparison to MMP-2 as revealed by gelatin zymogram and also by molecular docking studies. In many type of cells, activation of proMMP-2 occurs via an increase in the level of MT1-MMP (MMP-14). We, therefore, determined the interactions of MT1-MMP with the green tea catechins by molecular docking analysis. The study revealed a strong interaction of MT1-MMP with EGCG/ECG, and galloyl group has been observed to be responsible for the interaction.
- Subjects :
- Animals
Cattle
Humans
Muscle, Smooth, Vascular enzymology
Myocytes, Smooth Muscle enzymology
Catechin chemistry
Catechin pharmacology
Enzyme Precursors antagonists & inhibitors
Enzyme Precursors chemistry
Enzyme Precursors metabolism
Gelatinases antagonists & inhibitors
Gelatinases chemistry
Gelatinases metabolism
Matrix Metalloproteinase 2 chemistry
Matrix Metalloproteinase 2 metabolism
Molecular Docking Simulation
Protease Inhibitors chemistry
Protease Inhibitors pharmacology
Tea chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1573-4919
- Volume :
- 427
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Molecular and cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28013477
- Full Text :
- https://doi.org/10.1007/s11010-016-2903-y