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pKa Determination of a Histidine Residue in a Short Peptide Using Raman Spectroscopy

机译:用拉曼光谱法测定短肽中的组氨酸残基的pKa

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摘要

Determining the pKa of key functional groups is critical to understanding the pH-dependent behavior of biological proteins and peptide-based biomaterials. Traditionally, 1H NMR spectroscopy has been used to determine the pKa of amino acids; however, for larger molecules and aggregating systems, this method can be practically impossible. Previous studies concluded that the C-D stretches in Raman are a useful alternative for determining the pKa of histidine residues. In this study, we report on the Raman application of the C2-D probe on histidine’s imidazole side chain to determining the pKa of histidine in a short peptide sequence. The pKa of the tripeptide was found via difference Raman spectroscopy to be 6.82, and this value was independently confirmed via 1H NMR spectroscopy on the same peptide. The C2-D probe was also compared to other Raman reporters of the protonation state of histidine and was determined to be more sensitive and reliable than other protonation-dependent signals. The C2-D Raman probe expands the tool box available to chemists interested in directly interrogating the pKa’s of histidine-containing peptide and protein systems.
机译:确定关键官能团的pKa对了解生物蛋白和基于肽的生物材料的pH依赖性行为至关重要。传统上, 1 H NMR光谱法用于测定氨基酸的pKa。但是,对于较大的分子和聚集系统,该方法实际上是不可能的。先前的研究得出结论,拉曼中的C-D延伸是确定组氨酸残基pKa的有用替代方法。在这项研究中,我们报道了C2-D探针在组氨酸的咪唑侧链上的拉曼应用,以确定短肽序列中组氨酸的pKa。通过差拉曼光谱法发现三肽的pKa为6.82,并且该值通过同一肽上的 1 1 H NMR光谱法独立确认。还将C2-D探针与组氨酸的质子化状态的其他拉曼报道分子进行了比较,并确定它比其他依赖质子化的信号更为灵敏和可靠。 C2-D拉曼探针可扩展工具箱,供有兴趣直接询问含组氨酸肽和蛋白质系统pKa的化学家使用。

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