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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Luminescent protein staining with Re(I) tetrazolato complexes
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Luminescent protein staining with Re(I) tetrazolato complexes

机译:用Re(i)四唑酸盐配合物染色的发光蛋白质染色

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Within the general framework of our past and current studies dealing with the investigation of the photophysical properties and the biological behavior of the family of tetrazolato and tetrazole Re(I) complexes, we have endeavored to investigate their potential in the luminescent staining of proteins purified by acrylamide gel electrophoresis. With the aim to provide the first examples of luminescent Re(I) complexes to be exploited for this specific purpose, we have designed and prepared four new Re(I)-based species with the general formula fac-[Re(CO)(3)(N^N)(Tph)](2-/0), where Tph is the 5-(phenyl)tetrazolato anion and N^N is in turn represented by bathophenanthroline disulfonate (BPS), bathocuproine disulfonate (BCS) or by the SO3- free bathocuproine (BC). In this latter case, the neutral complex fac-[Re(CO)(3)(BC)(Tph)] served as a model species for the characterization of the former disulfonate complexes. Its cationic analogue fac-[Re(CO)(3)(BC)(Tph-Me)](+) was also prepared by a straightforward methylation reaction. All complexes displayed bright phosphorescence in organic media and, relative to their water solubility, the dianionic species fac-[Re(CO)(3)(BPS)(Tph)](2-) and fac-[Re(CO)(3)(BCS)(Tph)](2-) were also highly emissive in aqueous solution. The sulfonate groups played a key role in promoting and significantly enhancing the luminescent staining performances of both the Re(I) complexes fac-[Re(CO)(3)(BPS)(Tph)](2-) and fac-[Re(CO)(3)(BCS)(Tph)](2-) for proteins. Highlighting a response superior to that of Coomassie Blue and comparable to the one obtained by the well-known silver staining method, these dianionic Re(I)-complexes could efficiently detect up to 50 ng of pure Bovine Serum Albumin (BSA), as well as all proteins found in a Standard Protein Marker mix and from a total protein extract. A lower but still good response for luminescent protein staining was surprisingly obtained by employing the -SO3- free neutral and cationic comple
机译:在我们过去和目前研究的一般框架内,处理了四唑和四唑和四唑和四唑的生物行为的调查,我们致力于研究其在纯化的蛋白质的发光染色中的潜力丙烯酰胺凝胶电泳。旨在提供用于这种特定目的的发光Re(i)复合物的第一个实施例,我们设计并制定了四种新的RE(I)的物种,其中包含通式FAC-[RE(CO)(3 )(n ^,n)(tph)](2- / 0),其中Tph是5-(苯基)四唑啉阴离子和n = n又由Bankophyhanthroline二磺酸盐(BPS),浴缸CORONE表示二磺酸(BCS)或通过SO 3-无浴缸(BC)。在这种后一种情况下,中性复合体FAC-[RE(CO)(3)(BC)(TPH)]用作用于前二磺酸盐复合物的表征的模型物种。其阳离子类似物FAC-[RE(CO)(3)(3)(BC)(TPH-ME)](+)也通过直接的甲基化反应制备。所有复合物在有机培养基中显示出明亮的磷光,相对于它们的水溶性,Dianionic物种Fac-[Re(Co)(3)(BPS)(TPH)](2-)和Fac-[Re(Co)(3 )(BCS)(TPH)](2-)在水溶液中也高发射。磺酸盐基团在促进和显着增强Re(I)复合物Fac-[Re(Co)(3)(BPS)(TPH)](2-)和Fac中的发光染色性能方面发挥了关键作用蛋白质(共用)(3)(3)(BCS)(TPH)](2-)。突出显示Coomassie蓝色的反应和与通过众所周知的银染色方法获得的响应,这些Dianionic Re(i) - 互补物也可以有效地检测高达50ng的纯牛血清白蛋白(BSA)作为标准蛋白质标记物混合物中发现的所有蛋白质和总蛋白质提取物。通过使用-SO3 - 无中性和阳离子压力来令人惊讶地获得发光蛋白染色的较低但仍然良好的反应

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