RESUMEN
Human immunodeficiency virus 1 (HIV-1) therapeutic regimens consist of three or more drugs targeting different steps of the viral life cycle to limit the emergence of viral resistance. In line with the multitargeting strategy, here we conjugated a naphthalene diimide (NDI) moiety with a tetraazacycloalkane to obtain novel naphthalene diimide (NDI)-tetraazacycloalkane conjugates. The NDI inhibits the HIV-1 promoter activity by binding to LTR G-quadruplexes, and the tetraazacycloalkane mimics AMD3100, which blocks HIV entry into cells by interfering with the CXCR4 coreceptor. We synthesized, purified, and tested the metal-free NDI-tetraazacycloalkane conjugate and the two derived metal-organic complexes (MOCs) that incorporate Cu2+ and Zn2+. The NDI-MOCs showed enhanced binding to LTR G4s as assessed by FRET and CD assays in vitro. They also showed enhanced activity in cells where they dose-dependently reduced LTR promoter activity and inhibited viral entry only of the HIV-1 strain that exploited the CXCR4 coreceptor. The time of addition assay confirmed the dual targeting at the different HIV-1 steps. Our results indicate that the NDI-MOC conjugates can simultaneously inhibit viral entry, by targeting the CXCR4 coreceptor, and LTR promoter activity, by stabilizing the LTR G-quadruplexes. The approach of combining multiple targets in a single compound may streamline treatment regimens and improve the overall patient outcomes.
Asunto(s)
G-Cuádruplex , VIH-1 , Humanos , VIH-1/genética , Imidas/farmacología , Imidas/química , Imidas/metabolismo , Naftalenos/farmacología , Naftalenos/químicaRESUMEN
The ubiquitin E3 ligase substrate adapter cereblon (CRBN) is a target of thalidomide and lenalidomide1, therapeutic agents used in the treatment of haematopoietic malignancies2-4 and as ligands for targeted protein degradation5-7. These agents are proposed to mimic a naturally occurring degron; however, the structural motif recognized by the thalidomide-binding domain of CRBN remains unknown. Here we report that C-terminal cyclic imides, post-translational modifications that arise from intramolecular cyclization of glutamine or asparagine residues, are physiological degrons on substrates for CRBN. Dipeptides bearing the C-terminal cyclic imide degron substitute for thalidomide when embedded within bifunctional chemical degraders. Addition of the degron to the C terminus of proteins induces CRBN-dependent ubiquitination and degradation in vitro and in cells. C-terminal cyclic imides form adventitiously on physiologically relevant timescales throughout the human proteome to afford a degron that is endogenously recognized and removed by CRBN. The discovery of the C-terminal cyclic imide degron defines a regulatory process that may affect the physiological function and therapeutic engagement of CRBN.
Asunto(s)
Imidas , Proteolisis , Complejos de Ubiquitina-Proteína Ligasa , Humanos , Asparagina/química , Dipéptidos/farmacología , Glutamina/química , Imidas/química , Imidas/metabolismo , Lenalidomida/farmacología , Ligandos , Péptido Hidrolasas/metabolismo , Proteolisis/efectos de los fármacos , Proteoma/metabolismo , Talidomida/farmacología , Ubiquitinación/efectos de los fármacos , Secuencias de Aminoácidos , CiclizaciónRESUMEN
G-quadruplex existence was proved in cells by using both antibodies and small molecule fluorescent probes. However, the G-quadruplex probes designed thus far are structure- but not conformation-specific. Recently, a core-extended naphthalene diimide (cex-NDI) was designed and found to provide fluorescent signals of markedly different intensities when bound to G-quadruplexes of different conformations or duplexes. Aiming at evaluating how the fluorescence behaviour of this compound is associated with specific binding modes to the different DNA targets, cex-NDI was here studied in its interaction with hybrid G-quadruplex, parallel G-quadruplex, and B-DNA duplex models by biophysical techniques, molecular docking, and biological assays. cex-NDI showed different binding modes associated with different amounts of stacking interactions with the three DNA targets. The preferential binding sites were the groove, outer quartet, or intercalative site of the hybrid G-quadruplex, parallel G-quadruplex, and B-DNA duplex, respectively. Interestingly, our data show that the fluorescence intensity of DNA-bound cex-NDI correlates with the amount of stacking interactions formed by the ligand with each DNA target, thus providing the rationale behind the conformation-sensitive properties of cex-NDI and supporting its use as a fluorescent probe of G-quadruplex structures. Notably, biological assays proved that cex-NDI mainly localizes in the G-quadruplex-rich nuclei of cancer cells.
Asunto(s)
Adenocarcinoma/metabolismo , Neoplasias de la Mama/metabolismo , ADN Forma B/metabolismo , Colorantes Fluorescentes/química , Colorantes Fluorescentes/metabolismo , G-Cuádruplex , Imidas/química , Imidas/metabolismo , Sustancias Intercalantes/química , Sustancias Intercalantes/metabolismo , Conformación Molecular , Naftalenos/química , Naftalenos/metabolismo , Adenocarcinoma/patología , Sitios de Unión , Neoplasias de la Mama/patología , Supervivencia Celular/efectos de los fármacos , Femenino , Colorantes Fluorescentes/farmacología , Humanos , Imidas/farmacología , Concentración 50 Inhibidora , Sustancias Intercalantes/farmacología , Ligandos , Células MCF-7 , Espectroscopía de Resonancia Magnética/métodos , Simulación del Acoplamiento Molecular/métodos , Naftalenos/farmacologíaRESUMEN
Naphthalene diimides showed significant anticancer activity in animal models, with therapeutic potential related to their ability to strongly interact with G-quadruplexes. Recently, a trifunctionalized naphthalene diimide, named NDI-5, was identified as the best analogue of a mini-library of novel naphthalene diimides for its high G-quadruplex binding affinity along with marked, selective anticancer activity, emerging as promising candidate drug for in vivo studies. Here we used NMR, dynamic light scattering, circular dichroism and fluorescence analyses to investigate the interactions of NDI-5 with G-quadruplexes featuring either parallel or hybrid topology. Interplay of different binding modes of NDI-5 to G-quadruplexes was observed for both parallel and hybrid topologies, with end-stacking always operative as the predominant binding event. While NDI-5 primarily targets the 5'-end quartet of the hybrid G-quadruplex model (m-tel24), the binding to a parallel G-quadruplex model (M2) occurs seemingly simultaneously at the 5'- and 3'-end quartets. With parallel G-quadruplex M2, NDI-5 formed stable complexes with 1:3 DNA:ligand binding stoichiometry. Conversely, when interacting with hybrid G-quadruplex m-tel24, NDI-5 showed multiple binding poses on a single G-quadruplex unit and/or formed different complexes comprising two or more G-quadruplex units. NDI-5 produced stabilizing effects on both G-quadruplexes, forming complexes with dissociation constants in the nM range.
Asunto(s)
Antineoplásicos/metabolismo , ADN de Neoplasias/metabolismo , G-Cuádruplex , Guanina/metabolismo , Imidas/metabolismo , Naftalenos/metabolismo , Antineoplásicos/síntesis química , Secuencia de Bases , Sitios de Unión , ADN de Neoplasias/química , Guanina/química , Humanos , Imidas/síntesis química , Ligandos , Naftalenos/síntesis química , Soluciones , TermodinámicaRESUMEN
Nanocarrier-mediated protein delivery is a promising strategy for fundamental research and therapeutic applications. However, the efficacy of the current platforms for delivery into cells is limited by endosomal entrapment of delivered protein cargo with concomitantly inefficient access to the cytosol and other organelles, including the nucleus. We report here a robust, versatile polymeric-protein nanocomposite (PPNC) platform capable of efficient (≥90%) delivery of proteins to the cytosol. We synthesized a library of guanidinium-functionalized poly(oxanorborneneimide) (PONI) homopolymers with varying molecular weights to stabilize and deliver engineered proteins featuring terminal oligoglutamate "E-tags". The polymers were screened for cytosolic delivery efficiency using imaging flow cytometry with cytosolic delivery validated using confocal microscopy and activity of the delivered proteins demonstrated through functional assays. These studies indicate that the PPNC platform provides highly effective and tunable cytosolic delivery over a wide range of formulations, making them robust agents for therapeutic protein delivery.
Asunto(s)
Portadores de Fármacos/metabolismo , Integrasas/metabolismo , Proteínas Luminiscentes/metabolismo , Ácido Poliglutámico/metabolismo , Polímeros/metabolismo , Portadores de Fármacos/síntesis química , Guanidinas/síntesis química , Guanidinas/metabolismo , Células HEK293 , Células HeLa , Humanos , Imidas/síntesis química , Imidas/metabolismo , Nanocompuestos/química , Polímeros/síntesis química , Ingeniería de Proteínas , Proteína Fluorescente RojaRESUMEN
An organic semiconductor-bacteria biohybrid photosynthetic system is used to efficiently realize CO2 reduction to produce acetic acid with the non-photosynthetic bacteria Moorella thermoacetica. Perylene diimide derivative (PDI) and poly(fluorene-co-phenylene) (PFP) were coated on the bacteria surface as photosensitizers to form a p-n heterojunction (PFP/PDI) layer, affording higher hole/electron separation efficiency. The π-conjugated semiconductors possess excellent light-harvesting ability and biocompatibility, and the cationic side chains of organic semiconductors could intercalate into cell membranes, ensuring efficient electron transfer to bacteria. Moorella thermoacetica can thus harvest photoexcited electrons from the PFP/PDI heterojunction, driving the Wood-Ljungdahl pathway to synthesize acetic acid from CO2 under illumination. The efficiency of this organic biohybrid is about 1.6 %, which is comparable to those of reported inorganic biohybrid systems.
Asunto(s)
Ácido Acético/metabolismo , Dióxido de Carbono/metabolismo , Moorella/metabolismo , Fármacos Fotosensibilizantes/metabolismo , Energía Solar , Ácido Acético/química , Dióxido de Carbono/química , Transporte de Electrón , Fluorenos/química , Fluorenos/metabolismo , Imidas/química , Imidas/metabolismo , Estructura Molecular , Moorella/citología , Oxidación-Reducción , Perileno/análogos & derivados , Perileno/química , Perileno/metabolismo , Fármacos Fotosensibilizantes/química , Polímeros/química , Polímeros/metabolismo , Semiconductores , Propiedades de SuperficieRESUMEN
Implantation of synthetic small-diameter vascular bypass grafts is often associated with an increased risk of failure, due to thrombotic events or late intimal hyperplasia. As one of the causes an insufficient hemocompatibility of the artificial surface is discussed. Endothelialization of synthetic grafts is reported to be a promising strategy for creating a self-renewing and regulative anti-thrombotic graft surface. However, the establishment of a shear resistant cell monolayer is still challenging. In our study, cyto- and immuno-compatible poly(ether imide) (PEI) films were explored as potential biomaterial for cardiovascular applications. Recently, we reported that the initial adherence of primary human umbilical vein endothelial cells (HUVEC) was delayed on PEI-films and about 9 days were needed to establish a confluent and almost shear resistant HUVEC monolayer. To accelerate the initial adherence of HUVEC, the PEI-film surface was functionalized with an aptamer-cRGD peptide based endothelialization supporting system. With this functionalization the initial adherence as well as the shear resistance of HUVEC on PEI-films was considerable improved compared to the unmodified polymer surface. The in vitro results confirm the general applicability of aptamers for an efficient functionalization of substrate surfaces.
Asunto(s)
Aptámeros de Péptidos/metabolismo , Éter/metabolismo , Imidas/metabolismo , Polímeros/metabolismo , Técnicas de Cultivo de Célula , HumanosRESUMEN
Two novel solid reagents-1-sulfonimidoyl- and 1-sulfamimidoyl-3-methylimidazolium derivatives-for the synthesis of sulfonimidamides and imidosulfuric diamides, respectively, were developed. It is shown that these reagents are very effective in substitution reactions with various N- and O-nucleophiles; therefore, they significantly extend the accessibility to the chemical space covered by organosulfur(VI) compounds with S=N bonds. In addition, previously unknown imidosulfuric diamides with free imino nitrogen groups were prepared, and their physical and chemical properties were characterized (including molecular geometry, pKa , Log P, microsomal stability, and reactivity towards typical electrophiles). Similar to other organosulfur(VI) derivatives with S=N bonds, these compounds can be considered as promising bioisosteres of amides, ureas, or sulfonamides.
Asunto(s)
Diamida/síntesis química , Imidas/síntesis química , Sulfonamidas/síntesis química , Compuestos de Azufre/síntesis química , Animales , Técnicas de Química Sintética/métodos , Diamida/química , Diamida/metabolismo , Imidas/química , Imidas/metabolismo , Indicadores y Reactivos , Ratones , Microsomas/metabolismo , Modelos Moleculares , Sulfonamidas/química , Sulfonamidas/metabolismo , Compuestos de Azufre/química , Compuestos de Azufre/metabolismo , Difracción de Rayos XRESUMEN
A self-assembled multivalent glycosidase inhibitor based on perylene bisimide-deoxynojirimycin conjugates was constructed, inhibited α-mannosidase and exhibited a Ki value of 38 nM, increased approximately 2763-fold compared with the control drug (miglitol). Furthermore, the postprandial blood glucose (PBG) level in mice of PBI-DNJ was firstly studied. PBI-DNJ exhibited a hypoglycaemic effect in vivo. Importantly, this work developed a new means to explore the hypoglycaemic effect in mice based on self-assembled glycosidase inhibitors.
Asunto(s)
Glucosamina/análogos & derivados , Glicósido Hidrolasas/antagonistas & inhibidores , Imidas/metabolismo , Perileno/análogos & derivados , 1-Desoxinojirimicina/metabolismo , Animales , Glucosamina/metabolismo , Humanos , Ratones , Perileno/metabolismoRESUMEN
Amide-imide tautomerization presents a pervasive class of chemical transformations in organic chemistry of natural compounds. In this Perspective, we describe two distinctively different protein systems, in which the amide-imide tautomerization in the glutamine side chain takes place in enzymatic or photochemical reactions. First, hydrolysis of guanosine triphosphate (GTP) catalyzed by the Ras-GAP protein complex suggests the occurrence of the imide tautomer of glutamine in reaction intermediates. Second, photoexcitation of flavin-binding protein domains (BLUFs) initiates a chain of reactions in the chromophore-binding pocket, including amide-imide tautomerization of glutamine. Mechanisms of these reactions at the atomic level have been revealed in quantum mechanics/molecular mechanics (QM/MM) simulations. To reinforce conclusions on the critical role of amide-imide tautomerization of glutamine in these reactions we describe results of new quantum chemistry and QM/MM calculations for relevant molecular model systems. We reexamine results of the recent IR spectroscopy studies of BLUF domains, which provide experimental evidences of Gln tautomerization in proteins. We also propose to validate the glutamine-assisted mechanism of enzymatic GTP hydrolysis by using IR spectroscopy in a proper range of wavenumbers.
Asunto(s)
Amidas/química , Glutamina/química , Imidas/química , Proteínas Activadoras de ras GTPasa/química , Amidas/metabolismo , Glutamina/metabolismo , Hidrólisis , Imidas/metabolismo , Estructura Molecular , Procesos Fotoquímicos , Teoría Cuántica , Proteínas Activadoras de ras GTPasa/metabolismoRESUMEN
BACKGROUND: Risperidone is an antipsychotic drug. In blood, this drug binds mainly to human serum albumin (HSA) and is also transported by HSA. METHOD: To study certain details of the interaction between risperidone and HSA, a fluorescent dye CAPIDAN was used as a reporter. This dye specifically fluoresces from HSA in serum and is highly sensitive to structural changes in HSA including pathology-induced changes. Interaction of CAPIDAN with HSA has been studied using time-resolved fluorescence techniques. RESULT: The addition of phenylbutazone, a marker for the HSA drug-binding site I, leads to displacement of CAPIDAN from this site due to direct competition between phenylbutazone and the dye. The addition of risperidone induces a response of CAPIDAN fluorescence that is highly similar to its response to phenylbutazone. This response depends strongly on ionic strength and is very similar in both cases, phenylbutazone and risperidone. This similarity suggests that risperidone binds to HSA in the region of site I. In this site, the risperidone molecule probably covers the positive charge of Arginine 218 or Arginine 222 preventing their interaction with the CAPIDAN negatively charged carboxyl group. This effect was observed both in isolated HSA and in serum, suggesting similarity of the interaction. CONCLUSION: Thus, risperidone is able to prevent binding of organic anions (i.e. CAPIDAN as a drug-like molecule) to HSA.
Asunto(s)
Antipsicóticos/farmacología , Risperidona/farmacología , Albúmina Sérica Humana/metabolismo , Colorantes Fluorescentes/metabolismo , Humanos , Imidas/metabolismo , Naftalenos/metabolismo , Fenilbutazona/metabolismo , Unión ProteicaRESUMEN
Aggregation, red-NIR emission and light-up upon nucleic acid G-quadruplex binding have been investigated for a prototype core-extended naphthalene diimide, which is capable of fast cellular entry and nucleolar localization. Both high-level colocalization with an anti-G-quadruplex antibody and nucleolin displacement reveal that the compound targets and thus makes visible nuclear DNA G-quadruplexes.
Asunto(s)
Colorantes Fluorescentes/química , G-Cuádruplex , Anticuerpos/química , Anticuerpos/inmunología , Núcleo Celular/genética , Núcleo Celular/metabolismo , Proteínas Cromosómicas no Histona/inmunología , Colorantes Fluorescentes/metabolismo , Células HEK293 , Humanos , Imidas/química , Imidas/metabolismo , Microscopía Confocal , Naftalenos/química , Naftalenos/metabolismo , Espectrometría de FluorescenciaRESUMEN
Here we show that the active portion of a graphitic nanoparticle can be mimicked by a perylene diimide (PDI) to explain the otherwise elusive biological and electrocatalytic activity of the nanoparticle construct. Development of molecular analogues that mimic the antioxidant properties of oxidized graphenes, in this case the poly(ethylene glycolated) hydrophilic carbon clusters (PEG-HCCs), will afford important insights into the highly efficient activity of PEG-HCCs and their graphitic analogues. PEGylated perylene diimides (PEGn-PDI) serve as well-defined molecular analogues of PEG-HCCs and oxidized graphenes in general, and their antioxidant and superoxide dismutase-like (SOD-like) properties were studied. PEGn-PDIs have two reversible reduction peaks, which are more positive than the oxidation peak of superoxide (O2â¢-). This is similar to the reduction peak of the HCCs. Thus, as with PEG-HCCs, PEGn-PDIs are also strong single-electron oxidants of O2â¢-. Furthermore, reduced PEGn-PDI, PEGn-PDIâ¢-, in the presence of protons, was shown to reduce O2â¢- to H2O2 to complete the catalytic cycle in this SOD analogue. The kinetics of the conversion of O2â¢- to O2 and H2O2 by PEG8-PDI was measured using freeze-trap EPR experiments to provide a turnover number of 133 s-1; the similarity in kinetics further supports that PEG8-PDI is a true SOD mimetic. Finally, PDIs can be used as catalysts in the electrochemical oxygen reduction reaction in water, which proceeds by a two-electron process with the production of H2O2, mimicking graphene oxide nanoparticles that are otherwise difficult to study spectroscopically.
Asunto(s)
Grafito/química , Imidas/química , Nanopartículas/química , Perileno/análogos & derivados , Superóxido Dismutasa/química , Grafito/metabolismo , Peróxido de Hidrógeno/química , Peróxido de Hidrógeno/metabolismo , Interacciones Hidrofóbicas e Hidrofílicas , Imidas/metabolismo , Estructura Molecular , Óxidos/química , Óxidos/metabolismo , Perileno/química , Perileno/metabolismo , Polietilenglicoles/química , Polietilenglicoles/metabolismo , Superóxido Dismutasa/metabolismoRESUMEN
In this paper, novel polyimide/cellulose/TiO2 bionanocomposites (PI/BNCs) were prepared via a simple and inexpensive ultrasonic irradiation process. PI was synthesized by direct polycondensation reaction of novel monomer dianhydride with 4-(2-(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl)benzenamine. Due to the high surface energy and tendency for agglomeration the surface of nanoparticles was modified with cellulose. PI/BNCs containing 5, 10, and 15% of cellulose/TiO2 (BNCs) were successfully fabricated through ultrasonic irradiation technique. The obtained PI/BNCs were characterized by Fourier transform-infrared (FT-IR) spectroscopy, thermogravimetry analysis, X-ray powder diffraction, field emission-scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM). Thermogravimetric analysis data indicated an increase thermal stability of the PI/BNC polymers in compared to the pure polymer. From TEM image of PI/BNCs it can be found that the surface modified TiO2 with diametric size of less than 50nm, uniformly dispersed in the obtained PI matrix. The results obtained from gas permeation experiments with a constant pressure setup indicated that adding cellulose/TiO2 to the polymeric membrane structure increased the permeability of the membranes.
Asunto(s)
Celulosa/metabolismo , Imidas/química , Nanopartículas/química , Polímeros/química , Titanio/química , Celulosa/química , Imidas/metabolismo , Estructura Molecular , Nanopartículas/metabolismo , Tamaño de la Partícula , Polímeros/metabolismo , Propiedades de Superficie , Titanio/metabolismoRESUMEN
BACKGROUND: During the last decade, guanine G-rich sequences folding into G-quadruplex (G4) structures have received a lot of attention and their biological role is now a matter of large debate. Rising amounts of experimental evidence have validated several G-rich motifs as molecular targets in cancer treatment. Despite that an increasing number of small molecules has been reported to possess excellent G4 stabilizing properties, none of them has progressed through the drug-development pipeline due to their poor drug-like properties. In this context, the identification of G4 ligands with more favorable pharmacological properties and with a well-defined target activity could be fruitful for anticancer therapy application. SCOPE OF REVIEW: This manuscript outlines the current state of knowledge regarding EMICORON, a G4-interactive molecule structurally and biologically similar, on the one side, to coronene and, on the other side, to a bay-monosubstituted perylene. MAJOR CONCLUSIONS: Overall this work evidences that EMICORON, a new promising G4 ligand, possesses a marked antitumoral activity both standing alone and in combination with chemotherapeutics. Moreover, EMICORON represents a good example of multimodal class of antitumoral drug, able to simultaneously affect multiple targets participating in several distinct signaling pathways, thus simplifying the treatment modalities and improving the selectivity against cancer cells. GENERAL SIGNIFICANCE: Due to the importance of G4 forming sequences in crucial biological processes participating in tumor progression, their successful targeting with small molecules could represent a very important innovation in the development of effective therapeutic strategies against cancer. This article is part of a Special Issue entitled "G-quadruplex" Guest Editor: Dr. Concetta Giancola and Dr. Daniela Montesarchio.
Asunto(s)
Antineoplásicos/farmacología , Protocolos de Quimioterapia Combinada Antineoplásica/farmacología , ADN de Neoplasias/efectos de los fármacos , Diseño de Fármacos , G-Cuádruplex/efectos de los fármacos , Guanosina/metabolismo , Imidas/farmacología , Neoplasias/tratamiento farmacológico , Piperidinas/farmacología , Animales , Antineoplásicos/síntesis química , Antineoplásicos/metabolismo , Sitios de Unión , Proliferación Celular/efectos de los fármacos , ADN de Neoplasias/química , ADN de Neoplasias/genética , ADN de Neoplasias/metabolismo , Guanosina/química , Humanos , Imidas/síntesis química , Imidas/metabolismo , Ligandos , Modelos Moleculares , Neoplasias/genética , Neoplasias/metabolismo , Neoplasias/patología , Piperidinas/síntesis química , Piperidinas/metabolismo , Transducción de Señal/efectos de los fármacos , Relación Estructura-Actividad , Telómero/química , Telómero/efectos de los fármacos , Telómero/metabolismo , Carga Tumoral/efectos de los fármacosRESUMEN
BACKGROUND: Fluorescent sensing of G-quadruplex nucleic acids (G4s) is an effective strategy to elucidate their role in vitro and in vivo. Small molecule ligands have often been exploited, producing an emission light up upon binding. Naphthalene diimides (NDIs), although potent G4 binders exhibiting red-NIR fluorophores, have only been marginally exploited, as they are usually quenched upon binding. Contrary, aggregating core-extended naphthalene diimides (cex-NDIs) proved to be effective probes. METHODS: We prepared a library of eighteen cex-NDIs by organic synthesis, characterising their aggregation-dependent absorption and emission properties. Absorption and emission titrations, fluorescent intercalator displacement assay (FID) and circular dichroism (CD) analysis were performed to elucidate their behavior as G4 fluorescent sensors, selectivity and binding mode. RESULTS: cex-NDIs aggregate under aqueous solvents and as a result, their fluorescence is mostly quenched under physiological conditions. Upon G4 binding, they disaggregate into binding monomers, producing a fluorescent light-up with anti-parallel and hybrid G4s. Contrary, with parallel G4s a light-off was recorded. For the formers a groove-like interaction was inferred by ICD signals, while for the latter an end-stacking interaction mode was hypothesized by G4-FID data. CONCLUSIONS: cex-NDIs G4 sensing mechanism works via a induced disaggregation. The emission response depends on the G4 topology, which dictates the prevailing -groove or end-stacking- binding mode. GENERAL SIGNIFICANCE: This study highlights the potential of cex-NDIs as G4 fluorescent probes. Besides being readily synthesized and conveniently emitting above 600nm, they light-up upon binding to anti-parallel and hybrid G4, complementing a number of other probes' selectivity for the parallel topology. This article is part of a Special Issue entitled "G-quadruplex" Guest Editor: Dr. Concetta Giancola and Dr. Daniela Montesarchio.
Asunto(s)
ADN/metabolismo , Colorantes Fluorescentes/metabolismo , G-Cuádruplex , Guanosina/metabolismo , Imidas/metabolismo , Naftalenos/metabolismo , Sitios de Unión , Dicroismo Circular , ADN/química , Colorantes Fluorescentes/síntesis química , Guanosina/química , Concentración de Iones de Hidrógeno , Imidas/síntesis química , Ligandos , Naftalenos/síntesis química , Concentración Osmolar , Solventes/química , Espectrometría de Fluorescencia , Relación Estructura-ActividadRESUMEN
Accumulated uremic toxins like indoxyl sulphate, hippuric acid and p-cresyl sulphates in renal failure patients stimulate proinflammatory effects, and consequently kidney and cardiovascular diseases. Low clearance rate of these uremic toxins from the blood of uremic patients by conventional techniques like hemodialysis is due to their strong covalent albumin binding (greater than 95%) and hydrophobic nature, which led to alternatives like usage of hydrophobic adsorber's in removing these toxins from the plasma of kidney patients. Polymers like polyethylene, polyurethane, polymethylmethacrylate, cellophane and polytetrafluoroethylene were already in use as substitutes for metal devices as dialysis membranes. Among new synthetic polymers, one such ideal adsorber material are highly porous microparticles of poly(ether imide) (PEI) with diameters in the range from 50-180µm and a porosity around 88±2% prepared by a spraying and coagulation process.It is essential to make sure that these synthetic polymers should not evoke any inflammatory or apoptotic response during dialysis. Therefore in our study we evaluated in vitro effect of PEI microparticle extracts in human aortic endothelial cells (HEACs) concerning toxicity, inflammation and apoptosis. No cell toxicity was observed when HAECs were treated with PEI extracts and inflammatory/apoptotic markers were not upregulated in presence of PEI extracts. Our results ensure biocompatibility of PEI particles and further hemocompatibility of particles will be tested.
Asunto(s)
Células Endoteliales/metabolismo , Éter/metabolismo , Imidas/metabolismo , Polímeros/metabolismo , Insuficiencia Renal Crónica/genética , Insuficiencia Renal Crónica/metabolismo , Factor de Necrosis Tumoral alfa/metabolismo , HumanosRESUMEN
We report on the potential of a water-soluble tetracationic quaternary ammonium naphthalene diimide (NDI) as multifunctional agent of interest for theranostic applications. The DNA binding ability of this NDI has been investigated. NDI exhibits high binding constants for G-quadruplex DNA but it is not selective for this type of DNA. Taking advantage of its intrinsic fluorescence and singlet oxygen sensitizing ability, cellular uptake, cytotoxicity and photocytotoxicity have been investigated. The intense emission in the red/NIR allows monitoring of the cell permeability of this charged tetracationic NDI, accumulating into the cell nuclei. No dark cytotoxicity has been observed on selected tumor cell lines. Irradiation of the NDI loaded cells with red light reduces cell viability up to 40% and causes a significant increase of the percentage of cells expressing γH2AX foci indicating DNA damage. The presence of distinct DNA damage foci inside the nucleus suggests that the NDI molecule might induce DNA damage in specific sites. To the best of our knowledge this is the first NDI exhibiting PDT activity at µM concentration combined with low dark cytotoxicity.
Asunto(s)
Colorantes Fluorescentes/química , Colorantes Fluorescentes/toxicidad , Imidas/química , Imidas/toxicidad , Naftalenos/química , Naftalenos/toxicidad , Nanomedicina Teranóstica/métodos , Transporte Biológico , Línea Celular Tumoral , Supervivencia Celular , Análisis Diferencial Térmico/métodos , Colorantes Fluorescentes/metabolismo , G-Cuádruplex , Humanos , Imidas/metabolismo , Estructura Molecular , Naftalenos/metabolismo , Imagen Óptica , Procesos Fotoquímicos , Oxígeno Singlete/química , Relación Estructura-Actividad , TermodinámicaRESUMEN
Current haemodialysis techniques are not capable to remove efficiently low molecular weight hydrophobic uremic toxins from the blood of patients suffering from chronic renal failure. With respect to the hydrophobic characteristics and the high level of protein binding of these uremic toxins, hydrophobic adsorber materials might be an alternative to remove these substances from the plasma of the chronic kidney disease (CKD) patients. Here nanoporous microparticles prepared from poly(ether imide) (PEI) with an average diameter of 90 ± 30 µm and a porosity around 88 ± 2% prepared by a spraying/coagulation process are considered as candidate adsorber materials. A prerequisite for the clinical application of such particles is their biocompatibility, which can be examined i.e. indirectly in cell culture experiments with the particles' extracts. In this work we studied the effects of aqueous extracts of PEI microparticles on the viability of THP-1 cells, a human leukemia monocytic cell line, as well as their macrophage differentiation, reactive oxygen species (ROS) generation and inflammation.A high cell viability of around 99 ± 18% and 99 ± 5% was observed when THP-1 cells were cultured in the presence of aqueous extracts of the PEI microparticles in medium A and medium B respectively. The obtained microscopic data suggested that PEI particle extracts have no significant effect on cell death, oxidative stress or differentiation to macrophages. It was further found that the investigated proinflammatory markers in THP-1 cells were not up-regulated. These results are promising with regard to the biocompatibility of PEI microparticles and in a next step the hemocompatibility of the microparticles will be examined.
Asunto(s)
Éter/metabolismo , Imidas/metabolismo , Monocitos/metabolismo , Insuficiencia Renal Crónica/metabolismo , Micropartículas Derivadas de Células/metabolismo , Citotoxicidad Inmunológica , Humanos , Masculino , Estrés Oxidativo , Especies Reactivas de OxígenoRESUMEN
The permanent loss of cardiomyocytes may lead to the irreversible damage of myocardium in cardiovascular diseases. The induced pluripotent stem cells (iPSCs) with the capacity of differentiation into a variety of cell types including cardiomyocytes showed high potential for efficient heart regeneration. The iPSCs and iPSC-derived embryoid bodies (EBs) as well as the differentiated cardiomyocytes are highly sensitive to the biophysical cues of their microenvironment, and accordingly their behavior and function can be largely modulated by microstructure of the cell culture surface. In this study, we investigated the regulatory effect of microscale roughness on both cardiomyogenesis and secretion of EBs using poly(ether imide) (PEI) cell culture inserts with different levels of bottom roughness (R0: flat surface; R1: rough surface, Rq â¼ 4 µm; R2: rough surface, Rq â¼ 23 µm). The proliferation rate and cardiomyogenesis of EBs increased with the increase of surface roughness. The EB secretome derived from R2 surface remarkably enhanced the in vitro new vessel formation of endothelial cells, as compared to those from R0 and R1. These findings highlight the potential to improve the iPSC/EB-based restoration of cardiovascular function via microstructured biomaterials.