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1.
ACS Nano ; 14(5): 5956-5967, 2020 05 26.
Artigo em Inglês | MEDLINE | ID: mdl-32216328

RESUMO

Although antibodies remain a primary recognition element in all forms of biosensing, functional limitations arising from their size, stability, and structure have motivated the development and production of many different artificial scaffold proteins for biological recognition. However, implementing such artificial binders into functional high-performance biosensors remains a challenging task. Here, we present the design and application of Förster resonance energy transfer (FRET) nanoprobes comprising small artificial proteins (αRep bidomains) labeled with a Tb complex (Tb) donor on the C-terminus and a semiconductor quantum dot (QD) acceptor on the N-terminus. Specific binding of one or two protein targets to the αReps induced a conformational change that could be detected by time-resolved Tb-to-QD FRET. These single-probe FRET switches were used in a separation-free solution-phase assay to quantify different protein targets at sub-nanomolar concentrations and to measure the conformational changes with sub-nanometer resolution. Probing ligand-receptor binding under physiological conditions at very low concentrations in solution is a special feature of FRET that can be efficiently combined with other structural characterization methods to develop, understand, and optimize artificial biosensors. Our results suggest that the αRep FRET nanoprobes have a strong potential for their application in advanced diagnostics and intracellular live-cell imaging of ligand-receptor interactions.


Assuntos
Técnicas Biossensoriais , Pontos Quânticos , Transferência Ressonante de Energia de Fluorescência , Semicondutores , Térbio
2.
Environ Sci Technol ; 53(3): 1087-1097, 2019 02 05.
Artigo em Inglês | MEDLINE | ID: mdl-30605599

RESUMO

Lack of dynamic accounting in consequential life cycle assessment (CLCA) can keep policy-makers from having an accurate analysis of emission flows over time. In this study, we propose a dynamic CLCA framework to assess the environmental consequences of pavements. Dynamic changes in the demand vector and technosphere matrices were computed using relevant time horizons of affected supply technologies and incorporating time-dependent parameters. A Monte Carlo simulation was then conducted to propagate the variability, model uncertainty, and parameter uncertainty sources of LCI to the damage results. The results show that simplifying pavement CLCA framework through neglecting real-time changes results in notable diversions in the damage results. The environmental benefits of substituting asphalt with concrete are underestimated by 7, 17, and 77% for climate change, human health and resources categories, respectively. A divergence of 114% was also observed in ecosystem quality when using the static framework. Moreover, the lack of accounting for a temporal profile for GHG emissions using static characterization factors leads to a divergence of the GWP benefits of substituting asphalt with concrete of 473 t CO2eq (105%). The uncertainty results show 41-71% contribution of the variance in the damage categories is caused by the variability sources and is primarily attributed to monthly temperature accounting and service life.


Assuntos
Ecossistema , Formulação de Políticas , Método de Monte Carlo , Incerteza
3.
Chem Sci ; 9(42): 8046-8055, 2018 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-30542553

RESUMO

MicroRNAs (miRNAs) play an important role in cellular functions and in the development and progression of cancer. Precise quantification of endogenous miRNAs from different clinical patient and control samples combined with a one-to-one comparison to standard technologies is a challenging but necessary endeavor that is largely neglected by many emerging fluorescence technologies. Here, we present a simple, precise, sensitive, and specific ratiometric assay for absolute quantification of miRNAs. Isothermally amplified time-gated Förster resonance energy transfer (TG-FRET) between Tb donors and dye acceptors resulted in miRNA assays with single-nucleotide variant specificity and detection limits down to 4.2 ± 0.5 attomoles. Quantification of miR-21 from human tissues and plasma samples revealed the relevance for breast and ovarian cancer diagnostics. Analysis of miR-132 and miR-146a from acute monocytic leukemia cells (THP-1) demonstrated the broad applicability to different miRNAs and other types of clinical samples. Direct comparison to the gold standard RT-qPCR showed advantages of amplified TG-FRET concerning precision and specificity when quantifying low concentrations of miRNAs as required for diagnostic applications. Our results demonstrate that a careful implementation of rolling circle amplification and TG-FRET into one straightforward nucleic acid detection method can significantly advance the possibilities of miRNA-based cancer diagnostics and research.

4.
ACS Nano ; 10(2): 2591-9, 2016 Feb 23.
Artigo em Inglês | MEDLINE | ID: mdl-26845515

RESUMO

Nanoparticles combining enhanced cellular drug delivery with efficient fluorescence detection are important tools for the development of theranostic agents. Here, we demonstrate this concept by a simple, fast, and robust protocol of cationic polymer-mediated gold nanocluster (Au NCs) self-assembly into nanoparticles (NPs) of ca. 120 nm diameter. An extensive characterization of the monodisperse and positively charged NPs revealed pH-dependent swelling properties, strong fluorescence enhancement, and excellent colloidal and photostability in water, buffer, and culture medium. The versatility of the preparation is demonstrated by using different Au NC surface ligands and cationic polymers. Steady-state and time-resolved fluorescence measurements give insight into the aggregation-induced emission phenomenon (AIE) by tuning the Au NC interactions in the self-assembled nanoparticles using the pH-dependent swelling. In vitro studies in human monocytic cells indicate strongly enhanced uptake of the NPs compared to free Au NCs in endocytic compartments. The NPs keep their assembly structure with quite low cytotoxicity up to 500 µg Au/mL. Enhanced drug delivery is demonstrated by loading peptides or antibodies in the NPs using a one-pot synthesis. Fluorescence microscopy and flow cytometry confirmed intracellular colocalization of the biomolecules and the NP carriers with a respective 1.7-fold and 6.5-fold enhanced cellular uptake of peptides and antibodies compared to the free biomolecules.


Assuntos
Anticorpos/administração & dosagem , Portadores de Fármacos/química , Nanopartículas Metálicas/química , Oligopeptídeos/administração & dosagem , Linhagem Celular , Portadores de Fármacos/efeitos adversos , Ouro/química , Humanos , Nanopartículas Metálicas/efeitos adversos , Microscopia de Fluorescência/métodos , Poliaminas/efeitos adversos , Poliaminas/química , Polieletrólitos , Raios Ultravioleta
5.
Dalton Trans ; 43(41): 15583-92, 2014 Nov 07.
Artigo em Inglês | MEDLINE | ID: mdl-25204518

RESUMO

The synthesis of highly luminescent water soluble CdTe(x)S(y) quantum dots (QDs) is described and their elemental composition and optical properties are fully characterized. Glutathione (GSH)-capped nanocrystals were obtained from an aqueous solution of CdCl2, Na2TeO3 and GSH in the presence of NaBH4 upon heating at 100 °C. Spherical CdTe(x)S(y) alloyed nanoparticles with diameters ranging from 2 to 4 nm were formed, and characterized by X-ray powder diffraction and Transmission Electron Microscopy. Their elemental composition was determined from Inductively Coupled Plasma Atomic Emission Spectroscopy and CHN elemental analysis experiments. A model for the determination of their molecular formulas, molecular weights and extinction coefficients is proposed. Surface GSH molecules were involved in amide bond formation with fluorescent Nile-Red molecules, to be used as energy acceptor in Förster resonance energy transfer (FRET) experiments. FRET was observed from the CdTe(x)S(y) core (λ(ex) = 430 nm) to the Nile-Red dye (λ(em) = 648 nm) with an almost quantitative FRET efficiency (η(FRET) = 98%). A detailed analysis of the FRET is presented, revealing a core-dye distance of 24 Å, in very good agreement with the estimated radius of the core (13 Å) as measured by TEM. The QDs present excellent photophysical properties (QY up to 29%), easy synthesis and can be isolated as solids and redispersed in water without loss of their photoluminescence efficiency.

6.
Materials (Basel) ; 6(9): 4226-4248, 2013 Sep 23.
Artigo em Inglês | MEDLINE | ID: mdl-28788328

RESUMO

A constitutive model to describe the triaxial load-response spectrum of plain concrete in both tension and shear was developed. The inelastic phenomena are described using the plastic flow with direction determined by the gradient of the plastic potential. A new plastic potential is introduced and experimentally fitted to ensure better estimate of the load direction. This approach allows to control the inelastic dilatancy in terms of the inelastic deformation of the material. By overlaying the plastic potential on modified Etse and Willam's yield surface (both defined on the Haigh-Westergaard coordinates), the results showed that the two curves do not undergo similar stress states for a given strength level. It is, therefore, necessary that each surface goes through the current stress state to ensure adequate evaluation of normal vectors. A closed-form solution to accurately predict the triaxial stress state in concrete has been proposed. The predictive capabilities of the proposed model are evaluated by comparing predicted and measured stresses. The proposed model is shown to be accurate in predicting stress state of concrete.

7.
Dalton Trans ; 41(38): 11565-8, 2012 Oct 14.
Artigo em Inglês | MEDLINE | ID: mdl-22930162

RESUMO

A mixed valent copper complex [Cu(II)Cu(I)(L)(µ-SCN)(µ(3)-SCN)](n) (LH = N'-((pyridin-2-yl)methylene)acetohydrazide) has been synthesized and characterized. It is a unique example of a 2D mixed valent Cu(II)-Cu(I) interlinked molecular assembly with a very unusual bridging property of the hydrazone ligand. An extraordinary in situ partial Cu(II)→ Cu(I) reduction is observed in this system at room temperature.


Assuntos
Cobre/química , Hidrazonas/química , Complexos de Coordenação/química , Cristalografia por Raios X , Íons/química , Ligantes , Conformação Molecular , Piridinas/química , Temperatura
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