RESUMEN
The enzymes of the non-mevalonate pathway for isoprenoid biosynthesis have been identified as attractive targets with novel modes of action for the development of herbicides for crop protection and agents against infectious diseases. This pathway is present in many pathogenic organisms and plants, but absent in mammals. By using high-throughput screening, we identified highly halogenated marine natural products, the pseudilins, to be inhibitors of the third enzyme, IspD, in the pathway. Their activity against the IspD enzymes from Arabidopsis thaliana and Plasmodium vivax was determined in photometric and NMR-based assays. Cocrystal structures revealed that pseudilins bind to an allosteric pocket by using both divalent metal ion coordination and halogen bonding. The allosteric mode of action for preventing cosubstrate (CTP) binding at the active site was elucidated. Pseudilins show herbicidal activity in plant assays and antiplasmodial activity in cell-based assays.
Asunto(s)
Productos Biológicos/metabolismo , Ácido Mevalónico/metabolismo , Complejos Multienzimáticos/metabolismo , Proteínas de Plantas/metabolismo , Proteínas Protozoarias/metabolismo , Alcaloides/química , Alcaloides/metabolismo , Regulación Alostérica , Sitio Alostérico , Arabidopsis/enzimología , Sitios de Unión , Productos Biológicos/química , Halogenación , Herbicidas/química , Herbicidas/metabolismo , Espectroscopía de Resonancia Magnética , Simulación de Dinámica Molecular , Complejos Multienzimáticos/antagonistas & inhibidores , Proteínas de Plantas/antagonistas & inhibidores , Plasmodium vivax/enzimología , Estructura Terciaria de Proteína , Proteínas Protozoarias/antagonistas & inhibidoresAsunto(s)
Isomerasas Aldosa-Cetosa/antagonistas & inhibidores , Regulación Alostérica/efectos de los fármacos , Arabidopsis/enzimología , Inhibidores Enzimáticos/farmacología , Proteínas de Escherichia coli/antagonistas & inhibidores , Complejos Multienzimáticos/antagonistas & inhibidores , Oxidorreductasas/antagonistas & inhibidores , Pirimidinas/química , Pirimidinas/farmacología , Cristalografía por Rayos X , Inhibidores Enzimáticos/síntesis química , Inhibidores Enzimáticos/química , Modelos Moleculares , Estructura Molecular , Pirimidinas/síntesis química , Estereoisomerismo , Relación Estructura-ActividadRESUMEN
The dehydrogenation of 1-(4-hydroxyphenyl)-ethanol to 4-hydroxyacetophenone represents the second reaction step during anaerobic degradation of p-ethylphenol in the denitrifying bacterium 'Aromatoleum aromaticum' EbN1. Previous proteogenomic studies identified two different proteins (ChnA and EbA309) as possible candidates for catalyzing this reaction [Wöhlbrand et al: J Bacteriol 2008;190:5699-5709]. Physiological-molecular characterization of newly generated unmarked in-frame deletion and complementation mutants allowed defining ChnA (renamed here as Hped) as the enzyme responsible for 1-(4-hydroxyphenyl)-ethanol oxidation. Hped [1-(4-hydroxyphenyl)-ethanol dehydrogenase] belongs to the 'classical' family within the short-chain alcohol dehydrogenase/reductase (SDR) superfamily. Hped was overproduced in Escherichia coli, purified and crystallized. The X-ray structures of the apo- and NAD(+)-soaked form were resolved at 1.5 and 1.1 Å, respectively, and revealed Hped as a typical homotetrameric SDR. Modeling of the substrate 4-hydroxyacetophenone (reductive direction of Hped) into the active site revealed the structural determinants of the strict (R)-specificity of Hped (Phe(187)), contrasting the (S)-specificity of previously reported 1-phenylethanol dehydrogenase (Ped; Tyr(93)) from strain EbN1 [Höffken et al: Biochemistry 2006;45:82-93].
Asunto(s)
Alcohol Deshidrogenasa/química , Alcohol Deshidrogenasa/genética , Rhodocyclaceae/enzimología , Rhodocyclaceae/genética , Acetofenonas/química , Acetofenonas/metabolismo , Alcohol Deshidrogenasa/metabolismo , Sitios de Unión , Dominio Catalítico , Clonación Molecular , Cristalografía por Rayos X , Escherichia coli/enzimología , Escherichia coli/genética , Fermentación , Simulación del Acoplamiento Molecular/métodos , Mutación , Alcohol Feniletílico/análogos & derivados , Alcohol Feniletílico/química , Alcohol Feniletílico/metabolismo , Conformación Proteica , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Rhodocyclaceae/crecimiento & desarrollo , Análisis de Secuencia de ProteínaRESUMEN
Synthesis and SAR of orally active thrombin inhibitors of the d-Phe-Pro-Arg type with focus on the P2-moiety are described. The unexpected increase in in vitro potency, oral bioavailability, and in vivo activity of inhibitors with dehydroproline as P2-isostere is discussed. Over a period of 24h the antithrombin activity of the most active inhibitors with IC(50)s in the nanomolar range was determined in dogs demonstrating high thrombin inhibitory activity in plasma and an appropriate duration of action after oral administration.
Asunto(s)
Antitrombinas/farmacología , Administración Oral , Animales , Antitrombinas/administración & dosificación , Antitrombinas/síntesis química , Antitrombinas/farmacocinética , Disponibilidad Biológica , Perros , Relación Estructura-ActividadRESUMEN
The synthesis and SAR of novel nanomolar thrombin inhibitors with the common backbone HOOC-CH(2)-d-cyclohexylalanyl-3,4-dehydroprolyl-NH-CH(2)-aryl-C(=NH)NH(2) are described together with their ecarin clotting time (ECT) prolongation as measure for thrombin inhibition ex vivo. The aryl P1-moiety mimicking the arginine part of the d-Phe-Pro-Arg derived thrombin inhibitors turned out to be a key component for in vitro potency and in vivo activity. Optimization of this part led to compounds with improved antithrombin activity in rats and dogs after oral administration compared to the recently launched anticoagulant melagatran.
Asunto(s)
Antitrombinas/farmacología , Administración Oral , Animales , Antitrombinas/administración & dosificación , Antitrombinas/química , Perros , Modelos Moleculares , Ratas , Relación Estructura-Actividad , Difracción de Rayos XRESUMEN
(S)-1-Phenylethanol dehydrogenase (PED) from the denitrifying bacterium strain EbN1 catalyzes the NAD+-dependent, stereospecific oxidation of (S)-1-phenylethanol to acetophenone and the biotechnologically interesting reverse reaction. This novel enzyme belongs to the short-chain alcohol dehydrogenase/aldehyde reductase family. The coding gene (ped) was heterologously expressed in Escherichia coli and the purified protein was crystallized. The X-ray structures of the apo-form and the NAD+-bound form were solved at a resolution of 2.1 and 2.4 A, respectively, revealing that the enzyme is a tetramer with two types of hydrophobic dimerization interfaces, similar to beta-oxoacyl-[acyl carrier protein] reductase (FabG) from E. coli. NAD+-binding is associated with a conformational shift of the substrate binding loop of PED from a crystallographically unordered "open" to a more ordered "closed" form. Modeling the substrate acetophenone into the active site revealed the structural prerequisites for the strong enantioselectivity of the enzyme and for the catalytic mechanism. Studies on the steady-state kinetics of PED indicated a highly positive cooperativity of both catalytic directions with respect to the substrates. This is contrasted by the behavior of FabG. Moreover, PED exhibits extensive regulation on the enzyme level, being inhibited by elevated concentrations of substrates and products, as well as the wrong enantiomer of 1-phenylethanol. These regulatory properties of PED are consistent with the presence of a putative "transmission module" between the subunits. This module consists of the C-terminal loops of all four subunits, which form a special interconnected structural domain and mediate close contact of the subunits, and of a phenylalanine residue in each subunit that reaches out between substrate-binding loop and C-terminal domain of an adjacent subunit. These elements may transmit the substrate-induced conformational change of the substrate binding loop from one subunit to the others in the tetrameric complex and thus mediate the cooperative behavior of PED.
Asunto(s)
Bacterias/enzimología , Enoil-ACP Reductasa (NADH)/metabolismo , Escherichia coli/enzimología , Oxidorreductasas/química , Secuencia de Bases , Sitios de Unión , Biodegradación Ambiental , Cristalografía por Rayos X , Dimerización , Enoil-ACP Reductasa (NADH)/química , Interacciones Hidrofóbicas e Hidrofílicas , Cinética , NAD/química , NAD/metabolismo , Oxidorreductasas/aislamiento & purificación , Oxidorreductasas/metabolismo , Conformación Proteica , Estereoisomerismo , Especificidad por SustratoRESUMEN
Synthesis of thrombin inhibitors and their binding mode to thrombin is described. Modification of the P1 moiety leads to an increased selectivity versus trypsin. The observed selectivity is discussed in view of their thrombin-inhibitor complex X-ray structures.