SciELO - Scientific Electronic Library Online

 
vol.8 número2Estudio de las propiedades moleculares y reactivas del antibiótico Ciprofloxacina a nivel de Teoría de Funcional de Densidad DFT B3LYP/6-31G* índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

Compartir


Revista CON-CIENCIA

versión impresa ISSN 2310-0265

Resumen

BALLON PAUCARA, Wendy Guadalupe  y  GRADOS-TORREZ, Ricardo Enrique. Structural dynamics between the open and closed conformations of the KATP channel in pancreatic cells. Rev.Cs.Farm. y Bioq [online]. 2020, vol.8, n.2, pp.21-36. ISSN 2310-0265.

Abstract Introduction: The ATP-sensitive Potassium channel (KATP channel) regulates insulin production by pancreatic β cells. Glibenclamide (GBM) (antidiabetic drug) and ATP act as inhibitors of this channel, while ADP activates it. The KATP channel is an octamer consisting of 4 central Kir6.2 subunits that form the pore and 4 external regulation subunits SUR1. Objective: To determine the structural dynamics between the open and closed conformations of the KATP channel in pancreatic cells. Method: Comparative structural analysis of different crystallographic structures of the KATP channel of human pancreatic cells using Chimera v1.11.2. Results: The Kir6.2 subunit has a PIP2 binding domain (activator), an Interfacial Helix (IFH) and an N-terminal domain (KNtp). On the other hand, the SUR1 subunit that contains the GBM binding site, has 2 Nucleotide Binding Domains (NBD1/2), an M5-Lh1 loop and a Lasso Motif formed by the interface between the Trans-membrane Domain 0 and Loop 0 (TMD0-L0). The results of the dynamic structural analysis using bioinformatics tools indicate that these regions participate actively in the conformational changes that lead to the closure (inhibition) or opening (activation) of this channel. Conclusion: The study of the dynamics of activation and inhibition of the KATP channels is essential for the evaluation, discovery and/or design of new natural compounds, which like GBM, can promote insulin secretion to aid or improve the treatment of diabetic patients.

Palabras clave : KATP Channel; Structural Dynamics; Kir6.2; SUR1; Glibenclamide; ATP and ADP.

        · resumen en Español     · texto en Inglés     · Inglés ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons