Mechanistic Insights into PEPT1-Mediated Transport of a Novel Antiepileptic, NP-647 |
| |
Authors: | Kailas S Khomane Prajwal P Nandekar Banrida Wahlang Pravin Bagul Naeem Shaikh Yogesh B Pawar Chhuttan Lal Meena Abhay T Sangamwar Rahul Jain K Tikoo Arvind K Bansal |
| |
Affiliation: | Department of Pharmaceutics, ?Department of Pharmacoinformatics, §Department of Medicinal Chemistry, and ∥Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER) , Sector-67, SAS Nagar, Mohali, Punjab, India. |
| |
Abstract: | The present study, in general, is aimed to uncover the properties of the transport mechanism or mechanisms responsible for the uptake of NP-647 into Caco-2 cells and, in particular, to understand whether it is a substrate for the intestinal oligopeptide transporter, PEPT1 (SLC15A1). NP-647 showed a carrier-mediated, saturable transport with Michaelis-Menten parameters K(m) = 1.2 mM and V(max) = 2.2 μM/min. The effect of pH, sodium ion (Na(+)), glycylsarcosine and amoxicillin (substrates of PEPT1), and sodium azide (Na(+)/K(+)-ATPase inhibitor) on the flux rate of NP-647 was determined. Molecular docking and molecular dynamics simulation studies were carried out to investigate molecular interactions of NP-647 with transporter using homology model of human PEPT1. The permeability coefficient (P(appCaco-2)) of NP-647 (32.5 × 10(-6) cm/s) was found to be four times higher than that of TRH. Results indicate that NP-647 is transported into Caco-2 cells by means of a carrier-mediated, proton-dependent mechanism that is inhibited by Gly-Sar and amoxicillin. In turn, NP-647 also inhibits the uptake of Gly-Sar into Caco-2 cells and, together, this evidence suggests that PEPT1 is involved in the process. Docking and molecular dynamics simulation studies indicate high affinity of NP-647 toward PEPT1 binding site as compared to TRH. High permeability of NP-647 over TRH is attributed to its increased hydrophobicity which increases its affinity toward PEPT1 by interacting with the hydrophobic pocket of the transporter through hydrophobic forces. |
| |
Keywords: | |
本文献已被 PubMed 等数据库收录! |
|