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Benzimidazole, coumrindione and flavone derivatives as alternate UV laser desorption ionization (LDI) matrices for peptides analysis

机译:苯并咪唑,香豆二酮和黄酮衍生物可作为替代UV激光解吸电离(LDI)基质用于肽分析

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Background Matrix-assisted laser desorption/ionization (MALDI) is a soft ionization mass spectrometric technique, allowing the analysis of bio-molecules and other macromolecules. The matrix molecules require certain characteristic features to serve in the laser desorption/ionization mechanism. Therefore, only a limited number of compounds have been identified as ultraviolet- laser desorption/ionization (UV-LDI) matrices. However, many of these routine matrices generate background signals that useful information is often lost in them. We have reported flavones, coumarindione and benzimidazole derivatives as alternate UV-LDI matrices. Results Thirty one compounds have been successfully employed by us as matrices for the analysis of low molecular weight (LMW) peptides (up to 2000 Da). Two peptides, bradykinin and renin substrate tetra-decapeptide were analyzed by using the newly developed matrices. The MS measurements were made after mixing the matrix solution with analyte by using dried droplet sample preparation procedures. The synthesized matrix materials showed better S/N ratios and minimal background signals for low mass range. Furthermore, pico molar concentrations of [Glu1]-fibrinopeptide B human could be easily analyzed with these matrices. Finally, BSA-digest was analyzed and identified through database search against Swiss-Prot by using Mascot. Conclusions These results validate the good performance of the synthesized UV-laser desorption/ionization (LDI) matrices for the analysis of low molecular weight peptides.
机译:背景技术基质辅助激光解吸/电离(MALDI)是一种软电离质谱技术,可以分析生物分子和其他大分子。基质分子需要某些特征才能在激光解吸/电离机理中发挥作用。因此,仅将有限数量的化合物鉴定为紫外激光解吸/电离(UV-LDI)基质。但是,许多此类常规矩阵会生成背景信号,表明有用的信息经常会在其中丢失。我们报道了黄酮,香豆素二酮和苯并咪唑衍生物作为替代的UV-LDI基质。结果我们成功地使用了31种化合物作为分析低分子量(LMW)肽(最高2000 Da)的基质。使用新开发的基质分析了缓激肽和肾素底物四十肽这两种肽。在使用干滴样品制备程序将基质溶液与分析物混合后,进行MS测量。对于低质量范围,合成的基质材料显示出更好的信噪比和最小的背景信号。此外,使用这些基质可以轻松分析[Glu1]-纤维蛋白肽B人的皮摩尔浓度。最后,通过使用Mascot对Swiss-Prot进行数据库搜索来分​​析和识别BSA-digest。结论这些结果验证了合成的紫外激光解吸/电离(LDI)基质在分析低分子量肽方面的良好性能。

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