McPhie P
Laboratory of Biochemistry and Genetics, NIDDK, NIH, Building 8, Room 215, Bethesda, MD 20892-0830, USA.
Anal Biochem. 2001 Jun 1;293(1):109-19. doi: 10.1006/abio.2001.5113.
Estimates of the secondary structure of a protein in solution are made by mathematical analyses of its circular dichroism (CD) spectrum below 240 nm. All current procedures require accurate determination of the concentration of the protein sample. Insoluble proteins, such as prions or amyloid, are examined as thin films or gels, but concentrations cannot be precisely defined. The ratio of a sample's CD and absorbance signals is the g-factor, an intensive property. The g-factor spectra of 19 soluble, unconjugated proteins of known structures were measured and used to derive basis spectra, characteristic of the four major structural elements, helix, sheet, turn, and remainder. Using these, the g-factor spectra of other unconjugated proteins, measured in solution or as films, can be analyzed by linear regression to give good estimates of their secondary structures when protein concentration cannot be determined.
通过对蛋白质在240nm以下的圆二色性(CD)光谱进行数学分析,可估算其在溶液中的二级结构。目前所有的方法都需要准确测定蛋白质样品的浓度。不溶性蛋白质,如朊病毒或淀粉样蛋白,作为薄膜或凝胶进行检测,但浓度无法精确界定。样品的CD信号与吸光度信号之比为g因子,这是一种强度性质。测量了19种已知结构的可溶性、未结合蛋白质的g因子光谱,并用于推导基础光谱,这些光谱是螺旋、片层、转角和其余四种主要结构元件的特征。利用这些光谱,当无法确定蛋白质浓度时,通过线性回归分析,可以对在溶液中或作为薄膜测量的其他未结合蛋白质的g因子光谱进行分析,从而对其二级结构做出较好的估计。