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SYNTHETIC MOLECULES FOR LABELING HISTIDINE-RICH PROTEINS

机译:标记富含组氨酸蛋白的合成分子

摘要

The invention provides Zn-chelating compounds that are molecularly engineered to bind to a specific target sequence in a protein of interest. The Zn2+ ion is far less toxic and promiscuous than nickel and therefore provides an attractive alternative to Ni-based labeling systems. Invention Zn-chelating compounds also do not require oxidizable thiols and therefore can be used in non-reducing environments such as the surface of living cells. In addition, the target sequence is genetically encodable and requires incorporation of only a few amino acids, unlike fusions to fluorescent proteins such as GFP.
机译:本发明提供了锌螯合化合物,其经分子工程化以结合至目的蛋白质中的特定靶序列。 Zn 2+离子的毒性和混杂性远低于镍,因此提供了一种有吸引力的镍基标记系统替代品。本发明的锌螯合化合物也不需要可氧化的硫醇,因此可以用于非还原性环境,例如活细胞的表面。另外,靶序列是遗传可编码的,并且仅需要掺入几个氨基酸,这不同于与荧光蛋白例如GFP的融合。

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