MICRO-ENVIRONMENTAL SIGNATURE OF THE INTERACTIONS BETWEEN DRUGGABLE TARGET PROTEIN, DIPEPTIDYL PEPTIDASE-IV, AND ANTI-DIABETIC DRUGS

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CHAKRABORTY CHIRANJIB; MALLICK BIDYUT; SHARMA ASHISH RANJAN; SHARMA GARIMA; JAGGA SUPRIYA; PRIYA DOSS C GEORGE; NAM JU SUK; LEE SANG SOO

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Journal: Cell Journal (Yakhteh) Year:2017 | Volume:19 | Issue:1 Page(s): 65-83

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Title

MICRO-ENVIRONMENTAL SIGNATURE OF THE INTERACTIONS BETWEEN DRUGGABLE TARGET PROTEIN, DIPEPTIDYL PEPTIDASE-IV, AND ANTI-DIABETIC DRUGS

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Keywords

DIPEPTIDYL PEPTIDASE-IV (DPP-4)

SAXAGLIPTIN

LINAGLIPTIN

VILDAGLIPTIN

Abstract

Objective: Druggability of a target protein depends on the interacting micro-environment between the target protein and drugs. Therefore, a precise knowledge of the interacting micro-environment between the target protein and drugs is requisite for drug discovery process. To understand such micro-environment, we performed in silico interaction analysis between a human target protein, Dipeptidyl Peptidase-IV (DPP-4), and three anti-diabetic drugs (saxagliptin, LINAGLIPTIN and VILDAGLIPTIN).Materials and Methods: During the theoretical and bioinformatics analysis of micro-environmental properties, we performed drug-likeness study, protein active site predictions, docking analysis and residual interactions with the protein-drug interface. Micro-environmental landscape properties were evaluated through various parameters such as binding energy, intermolecular energy, electrostatic energy, van der Waals’+H-bond+desolvo energy (EVHD) and ligand efficiency (LE) using different in silico methods. For this study, we have used several servers and software, such as Molsoft prediction server, CASTp server, AutoDock software and LIGPLOT server.Results: Through micro-environmental study, highest log P value was observed for LINAGLIPTIN (1.07). Lowest binding energy was also observed for LINAGLIPTIN with DPP-4 in the binding plot. We also identified the number of H-bonds and residues involved in the hydrophobic interactions between the DPP-4 and the anti-diabetic drugs. During interaction, two H-bonds and nine residues, two H-bonds and eleven residues as well as four H-bonds and nine residues were found between the SAXAGLIPTIN, LINAGLIPTIN as well as VILDAGLIPTIN cases and DPP-4, respectively.Conclusion: Our in silico data obtained for drug-target interactions and micro-environmental signature demonstrates LINAGLIPTIN as the most stable interacting drug among the tested anti-diabetic medicines.

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APA: Copy

CHAKRABORTY, CHIRANJIB, MALLICK, BIDYUT, SHARMA, ASHISH RANJAN, SHARMA, GARIMA, JAGGA, SUPRIYA, PRIYA DOSS, C GEORGE, NAM, JU SUK, & LEE, SANG SOO. (2017). MICRO-ENVIRONMENTAL SIGNATURE OF THE INTERACTIONS BETWEEN DRUGGABLE TARGET PROTEIN, DIPEPTIDYL PEPTIDASE-IV, AND ANTI-DIABETIC DRUGS. CELL JOURNAL (YAKHTEH), 19(1), 65-83. SID. https://sid.ir/paper/694898/en

Vancouver: Copy

CHAKRABORTY CHIRANJIB, MALLICK BIDYUT, SHARMA ASHISH RANJAN, SHARMA GARIMA, JAGGA SUPRIYA, PRIYA DOSS C GEORGE, NAM JU SUK, LEE SANG SOO. MICRO-ENVIRONMENTAL SIGNATURE OF THE INTERACTIONS BETWEEN DRUGGABLE TARGET PROTEIN, DIPEPTIDYL PEPTIDASE-IV, AND ANTI-DIABETIC DRUGS. CELL JOURNAL (YAKHTEH)[Internet]. 2017;19(1):65-83. Available from: https://sid.ir/paper/694898/en

IEEE: Copy

CHIRANJIB CHAKRABORTY, BIDYUT MALLICK, ASHISH RANJAN SHARMA, GARIMA SHARMA, SUPRIYA JAGGA, C GEORGE PRIYA DOSS, JU SUK NAM, and SANG SOO LEE, “MICRO-ENVIRONMENTAL SIGNATURE OF THE INTERACTIONS BETWEEN DRUGGABLE TARGET PROTEIN, DIPEPTIDYL PEPTIDASE-IV, AND ANTI-DIABETIC DRUGS,” CELL JOURNAL (YAKHTEH), vol. 19, no. 1, pp. 65–83, 2017, [Online]. Available: https://sid.ir/paper/694898/en

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