Hutschenreiter Silke, Neumann Lars, Rädler Ulf, Schmitt Lutz, Tampé Robert
Institute of Biochemistry, Biocenter, Johann-Wolfgang-Goethe University Frankfurt, Marie-Curie Strasse 9, 60439 Frankfurt am Main, Germany.
Chembiochem. 2003 Dec 5;4(12):1340-4. doi: 10.1002/cbic.200200455.
Protein structure and function rely on a still not fully understood interplay of energetic and entropic constraints defined by the permutation of the twenty genetically encoded amino acids. Many attempts have been undertaken to design peptide-peptide interaction pairs and synthetic receptors de novo by using this limited number of building blocks. We describe a rational approach to creating a building block based on a tailored metal-chelating amino acid. Nepsilon,Nepsilon-bis(carboxymethyl)-L-lysine can be flexibly introduced into peptides by 9-fluorenylmethoxycarbonyl solid-phase chemistry. The corresponding metal-chelating peptides act as metal sensors and synthetic receptors for histidine-tagged proteins. These biochemical tweezers will open new ways to control protein-protein interactions, to design peptide-based interaction pairs, or to generate switchable protein function.
蛋白质的结构和功能依赖于由二十种遗传编码氨基酸的排列所定义的能量和熵约束之间尚未完全理解的相互作用。人们已经进行了许多尝试,通过使用这一有限数量的构建模块从头设计肽 - 肽相互作用对和合成受体。我们描述了一种基于定制的金属螯合氨基酸创建构建模块的合理方法。Nε,Nε - 双(羧甲基)-L - 赖氨酸可以通过芴甲氧羰基固相化学灵活地引入到肽中。相应的金属螯合肽可作为组氨酸标签蛋白的金属传感器和合成受体。这些生化镊子将为控制蛋白质 - 蛋白质相互作用、设计基于肽的相互作用对或产生可切换的蛋白质功能开辟新途径。