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1.
Mol Cell Proteomics ; 1(10): 805-15, 2002 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-12438563

RESUMO

Our experiments were designed to test the hypothesis that the cell surface interferon gamma receptor chains are preassembled rather than associated by ligand and to assess the molecular changes on ligand binding. To accomplish this, we used fluorescence resonance energy transfer, a powerful spectroscopic technique that has been used to determine molecular interactions and distances between the donor and acceptor. However, current commercial instruments do not provide sufficient sensitivity or the full spectra to provide decisive results of interactions between proteins labeled with blue and green fluorescent proteins in living cells. In our experiments, we used the blue fluorescent protein and green fluorescent protein pair, attached a monochrometer and charge-coupled device camera to a modified confocal microscope, reduced background fluorescence with the use of two-photon excitation, and focused on regions of single cells to provide clear spectra of fluorescence resonance energy transfer. In contrast to the prevailing view, the results demonstrate that the receptor chains are preassociated and that the intracellular domains move apart on binding the ligand interferon gamma. Application of this technology should lead to new rapid methods for high throughput screening and delineation of the interactome of cells.


Assuntos
Interferon gama/metabolismo , Receptores de Interferon/química , Animais , Células CHO , Células COS , Chlorocebus aethiops , Cricetinae , Transferência Ressonante de Energia de Fluorescência , Proteínas de Fluorescência Verde , Humanos , Ligantes , Proteínas Luminescentes/química , Microscopia Confocal , Microscopia de Fluorescência , Modelos Biológicos , Estrutura Terciária de Proteína , Receptores de Interferon/metabolismo , Espectrometria de Fluorescência
2.
Proteomics ; 2(4): 383-93, 2002 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12164697

RESUMO

Protein microarrays are considered an enabling technology, which will significantly expand the scope of current protein expression and protein interaction analysis. Current technologies, such as two-dimensional gel electrophoresis (2-DE) in combination with mass spectrometry, allowing the identification of biologically relevant proteins, have a high resolving power, but also considerable limitations. As was demonstrated by Gygi et al. (Proc. Nat. Acad. Sci. USA 2000,97, 9390-9395), most spots in 2-DE, observed from whole cell extracts, are from high abundance proteins, whereas low abundance proteins, such as signaling molecules or kinases, are only poorly represented. Protein microarrays are expected to significantly expedite the discovery of new markers and targets of pharmaceutical interest, and to have the potential for high-throughput applications. Key factors to reach this goal are: high read-out sensitivity for quantification also of low abundance proteins, functional analysis of proteins, short assay analysis times, ease of handling and the ability to integrate a variety of different targets and new assays. Zeptosens has developed a revolutionary new bioanalytical system based on the proprietary planar waveguide technology which allows us to perform multiplexed, quantitative biomolecular interaction analysis with highest sensitivity in a microarray format upon utilizing the specific advantages of the evanescent field fluorescence detection. The analytical system, comprising an ultrasensitive fluorescence reader and microarray chips with integrated microfluidics, enables the user to generate a multitude of high fidelity data in applications such as protein expression profiling or investigating protein-protein interactions. In this paper, the important factors for developing high performance protein microarray systems, especially for targeting low abundant messengers of relevant biological information, will be discussed and the performance of the system will be demonstrated in experimental examples.


Assuntos
Análise Serial de Proteínas , Proteínas/análise , Análise Serial de Proteínas/instrumentação , Análise Serial de Proteínas/métodos , Proteínas/química , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
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