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宽带多维光谱法鉴定家蚕丝膜中的酰胺 II 振动。

Broadband Multidimensional Spectroscopy Identifies the Amide II Vibrations in Silkworm Films.

机构信息

Department of Chemistry, Aarhus University, 8000 Aarhus C, Denmark.

Department of Materials Science and Engineering, University of Sheffield, Sheffield S1 3JD, UK.

出版信息

Molecules. 2022 Sep 23;27(19):6275. doi: 10.3390/molecules27196275.

Abstract

We used two-dimensional infrared spectroscopy to disentangle the broad infrared band in the amide II vibrational regions of native silk films, identifying the single amide II modes and correlating them to specific secondary structure. Amide I and amide II modes have a strong vibrational coupling, which manifests as cross-peaks in 2D infrared spectra with frequencies determined by both the amide I and amide II frequencies of the same secondary structure. By cross referencing with well-known amide I assignments, we determined that the amide II (N-H) absorbs at around 1552 and at 1530 cm for helical and β-sheet structures, respectively. We also observed a peak at 1517 cm that could not be easily assigned to an amide II mode, and instead we tentatively assigned it to a Tyrosine sidechain. These results stand in contrast with previous findings from linear infrared spectroscopy, highlighting the ability of multidimensional spectroscopy for untangling convoluted spectra, and suggesting the need for caution when assigning silk amide II spectra.

摘要

我们使用二维红外光谱技术来解析天然丝膜酰胺 II 振动区域中的宽红外带,确定了单个酰胺 II 模式,并将其与特定的二级结构相关联。酰胺 I 和酰胺 II 模式具有很强的振动耦合,这表现在二维红外光谱中的交叉峰上,其频率由同一二级结构的酰胺 I 和酰胺 II 频率决定。通过与已知的酰胺 I 分配的交叉参考,我们确定酰胺 II(N-H)在螺旋和β-折叠结构中分别在 1552 和 1530 cm 处吸收。我们还观察到一个在 1517 cm 处的峰,很难将其分配到酰胺 II 模式,而是我们暂定为酪氨酸侧链。这些结果与来自线性红外光谱的先前发现形成对比,突出了多维光谱技术用于解开复杂光谱的能力,并表明在分配丝酰胺 II 光谱时需要谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a783/9571984/a9665a8ec979/molecules-27-06275-g001.jpg

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