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Journal of Southern Medical University ; (12): 13-19, 2009.
Artículo en Chino | WPRIM | ID: wpr-339079

RESUMEN

<p><b>OBJECTIVE</b>To assess the binding activity of polypeptide containing human Na+, K+-ATPase alpha1 subunit M1-M2 extracellular segment (HES1 derivative).</p><p><b>METHODS</b>HES1 derivative was synthesized by Fmoc method and purified by high-performance liquid chromatography-mass spectrometry, and its binding activity was identified by radioligand binding assay.</p><p><b>RESULTS</b>3H-ouabain and synthetic HES1 derivative showed some binding activity with the equilibrium dissociation constant (KD) of 24.58 nmol/L, with the the receptor density of 492.43 fmol x mg(-1) pro. and IC50 of 3.078 x 10(-7) mol/L.</p><p><b>CONCLUSION</b>HES1 derivative can bind to ouabain and has the potential of becoming an effective therapeutic agent.</p>


Asunto(s)
Humanos , Sitios de Unión , Espacio Extracelular , Metabolismo , Ouabaína , Química , Farmacología , Péptidos , Química , Unión Proteica , ATPasa Intercambiadora de Sodio-Potasio , Química , Genética , Metabolismo
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