Center for Proteomics and Department of Pharmacology, Case Western Reserve University, Cleveland, Ohio 44106-4988, USA.
J Chem Phys. 2013 Jan 14;138(2):024112. doi: 10.1063/1.4774148.
A generalized method, termed Fast-SAXS-pro, for computing small angle x-ray scattering (SAXS) profiles of proteins, nucleic acids, and their complexes is presented. First, effective coarse-grained structure factors of DNA nucleotides are derived using a simplified two-particle-per-nucleotide representation. Second, SAXS data of a 18-bp double-stranded DNA are measured and used for the calibration of the scattering contribution from excess electron density in the DNA solvation layer. Additional test on a 25-bp DNA duplex validates this SAXS computational method and suggests that DNA has a different contribution from its hydration surface to the total scattering compared to RNA and protein. To account for such a difference, a sigmoidal function is implemented for the treatment of non-uniform electron density across the surface of a protein/nucleic-acid complex. This treatment allows differential scattering from the solvation layer surrounding protein/nucleic-acid complexes. Finally, the applications of this Fast-SAXS-pro method are demonstrated for protein/DNA and protein/RNA complexes.
本文提出了一种通用的方法,称为 Fast-SAXS-pro,用于计算蛋白质、核酸及其复合物的小角度 X 射线散射(SAXS)谱。首先,使用简化的两核苷酸/粒子表示法推导出 DNA 核苷酸的有效粗粒结构因子。其次,测量了 18 个碱基对的双链 DNA 的 SAXS 数据,并将其用于校准 DNA 溶剂化层中过剩电子密度的散射贡献。对 25 个碱基对 DNA 双链的额外测试验证了这种 SAXS 计算方法,并表明与 RNA 和蛋白质相比,DNA 对其水合表面的总散射有不同的贡献。为了考虑到这种差异,针对蛋白质/核酸复合物表面的非均匀电子密度,实现了一个 S 形函数。这种处理允许对蛋白质/核酸复合物周围的溶剂化层进行差分散射。最后,展示了这种 Fast-SAXS-pro 方法在蛋白质/DNA 和蛋白质/RNA 复合物中的应用。