RESUMO

P-glycoprotein (ABCB1) is an ATP-driven efflux pump which binds drugs within a large flexible binding pocket. Intrinsic Trp fluorescence was used to probe the interactions of LDS-751 (2-[4-(4-[dimethylamino]phenyl)-1,3-butadienyl]-3-ethylbenzo-thiazolium perchlorate) with purified P-glycoprotein, using steady-state/lifetime measurements and collisional quenching. The fast decay component of P-glycoprotein intrinsic fluorescence (tau(1)=0.97 ns) was unaffected by LDS-751 binding, while the slow decay component (tau(2)=4.02 ns) was quenched by dynamic and static mechanisms. Both the wavelength-dependence of the decay kinetics, and the time-resolved emission spectra, suggested the existence of excited-state relaxation processes within the protein matrix on the nanosecond time-scale, which were altered by LDS-751 binding. The fast decay component, which is more solvent-exposed, can be attributed to cytosolic/extracellular Trp residues, while the slow decay component likely arises from more buried transmembrane Trp residues. Interaction of a drug with the binding pocket of P-glycoprotein thus affects its molecular structure and fast dynamics.

Assuntos

RESUMO

The plasma membrane Ca(2+)-ATPase (PMCA) plays a key role in the regulation of the intracellular Ca(2+) concentration. Ethanol stimulates this Ca(2+) pump in an isoform-specific manner. On search for a physiological molecule that could mimic the effect of ethanol, we have previously demonstrated that some sphingolipids containing free "hydroxyl" groups, like ceramide, are able to stimulate the PMCA. Since diacylglycerol (DAG) structurally shares some characteristics with ceramide, we evaluate its effect on the PMCA. We demonstrated that DAG is a potent stimulator of this enzyme. The activation induced is additive to that produced by calmodulin, protein-kinase C and ethanol, which implies that DAG interacts with the PMCA through a different mechanism. Additionally, by different fluorescent approaches, we demonstrated a direct binding between PMCA and DAG. The results obtained in this work strongly suggest that DAG is a novel effector of the PMCA, acting by a direct interaction.

Assuntos

RESUMO

The P-glycoprotein efflux pump, an ABC superfamily member, can export a wide variety of hydrophobic drugs, natural products, and peptides from cells, powered by the energy of ATP hydrolysis. Transport substrates appear to first partition into the membrane and then interact with the protein within the cytoplasmic leaflet. Two drug binding sites within P-glycoprotein have been described which interact allosterically, the H-site (binds Hoechst 33342) and the R-site (binds rhodamine 123); however, the structural and functional relationship between the various binding sites appears complex. In this work, we have used fluorescence spectroscopic approaches to characterize the interaction of the transporter with LDS-751 and rhodamine 123, both of which are believed to bind to the putative R-site based on functional transport studies. By carrying out single and sequential dual fluorescence titrations of purified P-glycoprotein with the two substrates, we observed that bound LDS-751 interacted with bound rhodamine 123. Rhodamine 123 and LDS-751 showed a reciprocal negative interaction, each reducing the binding affinity of the other by 5-fold, indicating that the two compounds were simultaneously bound to the protein to form a ternary complex. Fitting of the dependence of the apparent Kd for LDS-751 binding on rhodamine 123 concentration suggested that the two compounds interacted noncompetitively. We conclude that the two-site drug binding model for P-glycoprotein requires modification. The putative R-site appears large enough to accommodate two compounds simultaneously. The locations where LDS-751 and rhodamine 123 bind are likely adjacent to each other, possibly overlapping, and may be within a hydrophobic pocket.

Assuntos

RESUMO

One cause of multidrug resistance is the overexpression of P-glycoprotein, a 170 kDa plasma membrane ABC transporter, which functions as an ATP-driven efflux pump with broad specificity for hydrophobic drugs, peptides, and natural products. The protein appears to interact with its substrates within the membrane environment. Previous reports suggested the existence of at least two binding sites, possibly overlapping and displaying positively cooperative interactions, termed the H and R sites for their preference for Hoechst 33342 and rhodamine 123, respectively. In this work, we have used several fluorescence approaches to characterize the molecular interaction of purified P-glycoprotein (Pgp) with the dye LDS-751, which is proposed to bind to the R site. A 50-fold enhancement of LDS-751 fluorescence indicated that the protein binding site was located in a hydrophobic environment, with a polarity lower than that of chloroform. LDS-751 bound with sub-micromolar affinity (K(d) = 0.75 microM) and quenched P-glycoprotein intrinsic Trp fluorescence by 40%, suggesting that Trp emitters are probably located close to the drub-binding regions of the transporter and may interact directly with the dye. Using a FRET approach, we mapped the possible locations of the LDS-751 binding site relative to the NB domain active sites. The R site appeared to be positioned close to the membrane boundary of the cytoplasmic leaflet. The location of both H and R drug binding sites is in agreement with the idea that Pgp may operate as a drug flippase, moving substrates from the inner leaflet to the outer leaflet of the plasma membrane.

Assuntos

RESUMO

El transportador multidrogas P-glicoproteína (Pgp) lleva a cabo el eflujo celular, ATP-dependiente, de muchas drogas hidrofóbicas, productos naturales y péptidos. Se propone que la Pgp contiene dos sitios de transporte, conocidos como los sitios -H y -R por sus preferencias por Hoechst 33342 (H33342) y rodamina 123, respectivamente. Cuando H33342 interactúa con la Pgp purificada, su rendimiento cuántico incrementa debido al ambiente hidrofóbico del bolsillo de enlazamiento –H. En este trabajo, estudiamos el enlazamiento de H33342 a la Pgp empleando experimentos cinéticos en la modalidad de stoppedflow. El curso temporal de la reacción fue seguido por el incremento de la fluorescencia del colorante y analizado con la herramienta computacional DYNAFIT, usando un modelo donde una reacción bimolecular rápida, es seguida por tres isomerizaciones secuenciales. Adicionalmente, bajo condiciones de seudo-primer-orden (exceso del ligando), la reacción presentó cuatro relajaciones caracterizadas por cuatro constantes de tiempo (á`s) y cuatro amplitudes (A¡`s) Estos parámetros fueron analizados utilizando la técnica de la matriz de los operadores de proyección. Esta aproximación aportó, por primera vez, información acerca de las constantes de velocidad y propiedades fluorescentes de los diversos intermediarios formados durante el enlazamiento de H33342 a la Pgp.

The P-glycoprotein multidrug transporter (Pgp) carries out ATP-driven cellular efflux of many different hydrophobic drugs, natural products, and peptides. Pgp is proposed to contain two drug transport sites, known as the H site and the R site for their preference for Hoechst 33342 (H33342) and rhodamine 123, respectively. When H33342 interacts with purified Pgp, its quantum yield is increased due to transfer to a hydrophobic environment within the H binding pocket, as shown by the steady-state fluorescence emission. In this work, we studied the binding of H33342 to Pgp using stopped-flow kinetic experiments. The time course of the reaction was followed by enhancement of dye fluorescence and analyzed by the computational tool DYNAFIT, using the model of a fast bimolecular reaction, followed by a three-step sequential isomerization. Additionally, under pseudo-first-order conditions (excess ligand), the reaction presented five normal modes, characterized by four relaxation times (á`s) and four amplitudes (A¡`s) These parameters were analyzed using the matrix projection operator technique, considering a four-step sequential reaction. This approach provides, for the first time, information about the rate constants and fluorescent properties of the diverse intermediates formed during the binding of H33342 to Pgp.

Assuntos