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Determination of the Solution Structure of AntifreezeGlycoproteins Using Two-Dimensional Infrared Spectroscopy

机译:防冻液溶液结构的确定二维红外光谱法测定糖蛋白

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摘要

We study the solution structure of antifreeze glycoproteins (AFGPs) with linear and two-dimensional infrared spectroscopy (2D-IR). With 2D-IR, we study the coupling between the amide I and amide II vibrations of AFGPs. The measured nonlinear spectral response constitutes a much more clearly resolved amide I spectrum than the linear absorption spectrum of the amide I vibrations and allows us to identify the different structural elements of AFGPs in solution. We find clear evidence for the presence of polyproline II (PPII) helical structures already at room temperature, and we find that the fraction of PPII structures increases when the temperature is decreased to the biological working temperature of AFGP. We observe that inhibition of the antifreeze activity of AFGP using borate buffer or enhancing the antifreeze activity using sulfate buffer does not lead to significant changes in the protein conformation. This finding indicates that AFGPs bind to ice with their sugar side chains.
机译:我们用线性和二维红外光谱(2D-IR)研究了抗冻糖蛋白(AFGPs)的溶液结构。利用2D-IR,我们研究了AFGP的酰胺I和酰胺II振动之间的耦合。与酰胺I振动的线性吸收光谱相比,所测得的非线性光谱响应所构成的酰胺I光谱要清晰得多,这使我们能够识别溶液中AFGP的不同结构元素。我们发现在室温下已经存在聚脯氨酸II(PPII)螺旋结构的明确证据,并且我们发现,当温度降低到AFGP的生物学工作温度时,PPII结构的比例增加。我们观察到使用硼酸盐缓冲液抑制AFGP的抗冻活性或使用硫酸盐缓冲液增强抗冻活性不会导致蛋白质构象发生重大变化。该发现表明AFGPs通过其糖侧链与冰结合。

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