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首页> 外文期刊>Journal of proteomics >Mass spectrometry based approach for identification and characterisation of fluorescent proteins from marine organisms.
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Mass spectrometry based approach for identification and characterisation of fluorescent proteins from marine organisms.

机译:基于质谱的方法来鉴定和表征来自海洋生物的荧光蛋白。

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We present here a new analytical strategy for identification and characterisation of fluorescent proteins from marine organisms. By applying basic proteomics tools it is possible to screen large sample collections for fluorescent proteins of desired characteristics prior to gene cloning. Our methodology which includes isolation, spectral characterisation, stability testing, gel-based separation and mass spectrometric identification was optimised on samples collected during the Danish Galathea 3 expedition. Four corals of the Fungia, Sarcophyton and Acropora species emitting green fluorescence were tested. Each of the fluorescent extracts behaves differently under denaturing conditions but complete fluorescence loss was not observed. Optimised electrophoretic conditions yielded effective separation of active fluorescent proteins in both 1DE and 2DE. Mass spectrometric analysis of the proteins in the fluorescent spots excised directly from unstained 2DE gels provides sequence information that might be sufficient to design degenerate primers for gene cloning. Identified fluorescent proteins are in agreement with the coral species determined by visual examination of the samples. The presented methodology is a viable alternative to direct gene cloning for the discovery of novel fluorescent proteins and will be further validated on other samples collected during the Galathea 3 expedition.
机译:我们在这里提出了一种新的分析策略,用于鉴定和表征来自海洋生物的荧光蛋白。通过应用基本的蛋白质组学工具,可以在基因克隆之前针对所需特性的荧光蛋白筛选大量样品。我们对丹麦Galathea 3探险队收集的样品进行了优化,包括分离,光谱表征,稳定性测试,基于凝胶的分离和质谱鉴定等方法。测试了发出绿色荧光的Fungia,Sarcophyton和Acropora物种的4种珊瑚。每种荧光提取物在变性条件下的行为都不同,但未观察到完全的荧光损失。优化的电泳条件可有效分离1DE和2DE中的活性荧光蛋白。直接从未染色的2DE凝胶中切除的荧光斑点中的蛋白质的质谱分析提供了可能足以设计用于基因克隆的简并引物的序列信息。鉴定出的荧光蛋白与通过目测检查确定的珊瑚种类一致。提出的方法是直接基因克隆的一种可行替代方法,用于发现新型荧光蛋白,并将在Galathea 3探险期间收集的其他样品上得到进一步验证。

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