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Total protein concentration quantification using nanobeads with a new highly luminescent terbium(iii) complex

机译:使用纳米孔的总蛋白质浓度定量,具有新的高亮铽(III)复合物

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Total protein concentration (TPC) is a key parameter in many biochemical experiments and its quantification is often necessary for isolation, separation, and analysis of proteins. A sensitive and rapid nanobead-based TPC quantification assay based on F?rster Resonance Energy Transfer (FRET) has been developed. A new, highly luminescent Tb( III ) complex has been synthesised and applied as donor in this FRET assay with an organic dye (Cy5) as acceptor. FRET-induced changes in luminescence have been investigated both at donor and acceptor emission wavelength using time-resolved luminescence spectroscopy with time-gated detection. In the assay, the Tb( III ) complex and fine-tuned polyglycidyl methacrylate (PGMA) nanobeads ensure that an improvement in sensitivity and background reduction is achieved. Using 40 nm large PGMA nanobeads loaded with the Tb( III ) complex, it is possible to determine TPC down to 50 ng mL ~(?1) in just 10 minutes. Through specific assay components the sensitivity has been improved when compared to existing nanobead-based assays and to currently known commercial methods. Additionally, the assay is relatively insensitive to the presence of contaminants, such as non-ionic detergents commonly found in biological samples. Due to no need for any centrifugal steps, this mix-and-measure bioassay can easily be implemented into routine TPC quantification protocols in biochemical laboratories.
机译:总蛋白质浓度(TPC)是许多生物化学实验中的关键参数,其定量通常是分离,分离和分析蛋白质的必要条件。已经开发了一种基于F?奔跑谐振能量转移(FRET)的敏感和快速的基于纳米的TPC定量测定。已经合成了一种新的高发致发光的TB(III)络合物,并用作有机染料(CY5)作为受体作为受体的供体。使用时间分辨的发光光谱,在施主和受体发射波长中研究了发光的诱导变化,使用时间升定的发光光谱,具有时间门控检测。在测定中,Tb(III)复合物和微调的聚缩氟基甲基丙烯酸酯(PGMA)纳米甲基甲酸酯确保实现了敏感性和背景降低的改善。使用加载与Tb(III)复合物的40nm大的PGMA纳米珠,只需10分钟即可将TPC降至50ng〜(β1)。通过特异性测定组分,与现有的基于纳米孔的测定和当前已知的商业方法相比,敏感性已经提高。另外,测定对污染物的存在相对不敏感,例如在生物样品中常见的非离子洗涤剂。由于不需要任何离心步骤,这种混合和测量的生物测定可以容易地在生化实验室中的常规TPC定量方案中实施。

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