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Assessing the Impact of Synchrotron X-ray Irradiation on Proteinaceous Specimens at Macro and Molecular Levels

机译:在宏观和分子水平上评估同步加速器X射线辐照对蛋白质样本的影响

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Synchrotron radiation (SR) has become a preferred technique for the analysis of a wide range of archeological samples, artwork, and museum specimens. While SR is called a nondestructive technique, its effect on proteinaceous specimens has not been fully investigated at the molecular level. To investigate the molecular level effects of synchrotron X-ray on proteinaceous specimens, we propose a methodology where four variables are considered: (1) type of specimen: samples ranging from amino acids to proteinaceous objects such as silk, wool, parchment, and rabbit skin glue were irradiated; (2) synchrotron X-ray energy; (3) beam intensity; (4) irradiation time. Irradiated specimens were examined for both macroscopic and molecular effects. At macroscopic levels, color change, brittleness, and solubility enhancement were observed for several samples within 100 s of irradiation. At molecular levels, the method allowed one to quantify significant amino acid modifications. Aspartic acid (Asp), wool, parchment, and rabbit skin glue showed a significant increase in Asp racemization upon increasing irradiation time with rabbit skin glue showing the greatest increase in D-Asp formation. In contrast, Asp in silk, pure cystine (dimer of cysteine), and asparagine (Asn) did not show signs of racemization at the irradiation times studied; however, the latter two compounds showed significant signs of decomposition. Parchment and rabbit skin glue exhibited racemization of Asp, as well as racemization of isoleucine (Ile) and phenylalanine (Phe) after 100 s of irradiation with a focused beam. Under the experimental conditions and sample type and dimensions used here, more change was observed for focused and low energy (8 keV) beams than unfocused or higher energy (22 keV) beams. These results allow quantification of the change induced at the molecular level on proteinaceous specimens by synchrotron X-ray radiation and help to define accurate thresholds to minimize the probability of damage occurring to cultural heritage specimens. For most samples, damage was usually observed in the 1-10 s time scale, which is about an order of magnitude longer than SR studies of cultural heritage under X-ray fluorescence (XRF) mode; however, it is consistent with the duration of X-ray absorption spectroscopy (XAS) and microcomputed tomography (μCT) measurements.
机译:同步辐射(SR)已成为分析各种考古样品,艺术品和博物馆标本的首选技术。虽然SR被称为非破坏性技术,但其在蛋白质标本上的作用尚未在分子水平上得到充分研究。为了研究同步加速器X射线对蛋白质标本的分子水平影响,我们提出了一种方法,其中考虑了四个变量:(1)标本类型:从氨基酸到蛋白质物体(如丝绸,羊毛,羊皮纸和兔子)的样本辐照了皮肤胶; (2)同步加速器的X射线能量; (3)光束强度; (4)照射时间。检查辐照样品的宏观和分子效应。在宏观水平上,在辐射100 s内观察到一些样品的颜色变化,脆性和溶解度增强。在分子水平上,该方法允许人们量化显着的氨基酸修饰。随着辐照时间的增加,天冬氨酸(Asp),羊毛,羊皮纸和兔子皮胶显示出Asp外消旋的显着增加,其中兔子皮胶显示出D-Asp形成的最大增加。相反,在所研究的照射时间下,丝中的Asp,纯胱氨酸(半胱氨酸的二聚体)和天冬酰胺(Asn)没有显示消旋的迹象。然而,后两种化合物显示出明显的分解迹象。在聚焦光束照射100 s后,羊皮纸和兔皮胶表现出Asp的消旋化,以及异亮氨酸(Ile)和苯丙氨酸(Phe)的消旋化。在此处使用的实验条件以及样品类型和尺寸下,与未聚焦或更高能量(22 keV)的光束相比,聚焦和低能量(8 keV)的光束观察到更多变化。这些结果可以量化同步加速器X射线辐射在蛋白质标本上在分子水平上引起的变化,并有助于定义准确的阈值,以最大程度地减少文化遗产标本受到破坏的可能性。对于大多数样品,通常在1-10 s的时间范围内观察到损坏,这比在X射线荧光(XRF)模式下对文化遗产进行的SR研究要长大约一个数量级。但是,它与X射线吸收光谱(XAS)和微计算机断层扫描(μCT)测量的持续时间一致。

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