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1.
J Mol Recognit ; 24(2): 220-34, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-20540076

RESUMEN

The diuretic drug ethacrynic acid (EA), both an inhibitor and substrate of pi class glutathione S-transferase (GST P1-1), has been tested in clinical trials as an adjuvant in chemotherapy. We recently studied the role of the active site residue Tyr-108 in binding EA to the enzyme and found that the analysis was complicated by covalent binding of this drug to the highly reactive Cys-47. Previous attempts to eliminate this binding by chemical modification yielded ambiguous results and therefore we decided here to produce a double mutant C47S/Y108V by site directed mutagenesis and further expression in Escherichia coli and the interaction of EA and its GSH conjugate (EASG) examined by calorimetric studies and X-ray diffraction. Surprisingly, in the absence of Cys-47, Cys-101 (located at the dimer interface) becomes a target for modification by EA, albeit at a lower conjugation rate than Cys-47. The Cys-47 → Ser mutation in the double mutant enzyme induces a positive cooperativity between the two subunits when ligands with affinity to G-site bind to enzyme. However, this mutation does not seem to affect the thermodynamic properties of ligand binding to the electrophilic binding site (H-site) and the thermal or chemical stability of this double mutant does not significantly affect the unfolding mechanism in either the absence or presence of ligand. Crystal structures of apo and an EASG complex are essentially identical with a few exceptions in the H-site and in the water network at the dimer interface.


Asunto(s)
Cisteína/genética , Diuréticos/metabolismo , Ácido Etacrínico/metabolismo , Gutatión-S-Transferasa pi/química , Gutatión-S-Transferasa pi/metabolismo , Proteínas Mutantes/metabolismo , Mutación/genética , Sustitución de Aminoácidos , Calorimetría , Cristalografía por Rayos X , Activación Enzimática , Glutatión/metabolismo , Humanos , Concentración de Iones de Hidrógeno , Cinética , Modelos Moleculares , Proteínas Mutantes/química , Multimerización de Proteína , Relación Estructura-Actividad , Especificidad por Sustrato , Termodinámica
2.
Biometrics ; 66(2): 578-85, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19645702

RESUMEN

A functional regression model to forecast the cypress pollen concentration during a given time interval, considering the air temperature in a previous interval as the input, is derived by means of a two-step procedure. This estimation is carried out by functional principal component (FPC) analysis and the residual noise is also modeled by FPC regression, taking as the explicative process the pollen concentration during the earlier interval. The prediction performance is then tested on pollen data series recorded in Granada (Spain) over a period of 10 years.


Asunto(s)
Monitoreo del Ambiente/estadística & datos numéricos , Predicción , Modelos Estadísticos , Polen , Cupressus , Análisis de Componente Principal , Análisis de Regresión , Estaciones del Año , España , Temperatura
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