Maia Raiza N A, Mitra Sunayana, Baiz Carlos R
Department of Chemistry, University of Texas at Austin, Austin, TX 78712-1224, USA.
MethodsX. 2023 Aug 1;11:102309. doi: 10.1016/j.mex.2023.102309. eCollection 2023 Dec.
Fourier-transform infrared (FTIR) spectroscopy using vibrational probes is an ideal tool to detect changes in structure and local environments within biological molecules. However, challenges arise when dealing with weak infrared probes, such as thiocyanates, due to their inherent low signal strengths and overlap with solvent bands. In this protocol we demonstrate:•A streamlined approach for the precise extraction of weak infrared absorption lineshapes from a strong solvent background.•A protocol combining a spectral filter, background modeling, and subtraction.•Our methodology successfully extracts the CN stretching mode peak from methyl thiocyanate at remarkably low concentrations (0.25 mM) in water, previously a challenge for FTIR spectroscopy.This approach offers valuable insights and tools for more accurate FTIR measurements using weak vibrational probes. This enhanced precision can potentially enable new approaches to enhance our understanding of protein structure and dynamics in solution.
使用振动探针的傅里叶变换红外(FTIR)光谱是检测生物分子结构和局部环境变化的理想工具。然而,在处理诸如硫氰酸盐等弱红外探针时会出现挑战,这是由于它们固有的低信号强度以及与溶剂谱带的重叠。在本方案中,我们展示了:
• 一种从强溶剂背景中精确提取弱红外吸收线形的简化方法。
• 一种结合光谱滤波、背景建模和减法的方案。
• 我们的方法成功地从水中浓度极低(0.25 mM)的硫氰酸甲酯中提取出CN伸缩模式峰,这在以前对于FTIR光谱来说是一项挑战。
这种方法为使用弱振动探针进行更精确的FTIR测量提供了有价值的见解和工具。这种提高的精度有可能带来新的方法,以增强我们对溶液中蛋白质结构和动力学的理解。