Dipartimento di Chimica, Università degli Studi di Bari Aldo Moro, Via Orabona, 4, 70126 Bari, Italy.
Anal Chim Acta. 2013 Oct 10;798:56-63. doi: 10.1016/j.aca.2013.08.050. Epub 2013 Sep 6.
The effectiveness of a novel binary matrix composed of 1,8-bis(dimethylamino)naphthalene (DMAN; proton sponge) and 9-aminoacridine (9AA) for the direct lipid analysis of whole bacterial cells by matrix assisted laser desorption ionization mass spectrometry (MALDI MS) is demonstrated. Deprotonated analyte signals nearly free of matrix-related ions were observed in negative ion mode. The effect of the most important factors (laser energy, pulse voltage, DMAN/9AA ratio, analyte/matrix ratio) was investigated using a Box-Behnken response surface design followed by multi-response optimization in order to simultaneously maximize signal-to-noise (S/N) ratio and resolution. The chemical surface composition of single or mixed matrices was explored by X-ray photoelectron spectroscopy (XPS). Moreover, XPS imaging was used to map the spatial distribution of a model phospholipid in single or binary matrices. The DMAN/9AA binary matrix was then successfully applied to the analysis of intact Gram positive (Lactobacillus sanfranciscensis) or Gram negative (Escherichia coli) microorganisms. About fifty major membrane components (free fatty acids, mono-, di- and tri-glycerides, phospholipids, glycolipids and cardiolipins) were quickly and easily detected over a mass range spanning from ca. 200 to ca. 1600 m/z. Moreover, mass spectra with improved S/N ratio (compared to single matrices), reduced chemical noise and no formation of matrix-clusters were invariably obtained demonstrating the potential of this binary matrix to improve sensitivity.
证明了由 1,8-双(二甲氨基)萘(DMAN;质子海绵)和 9-氨基吖啶(9AA)组成的新型二元基质对于通过基质辅助激光解吸电离质谱(MALDI MS)直接分析全细菌细胞的脂质的有效性。在负离子模式下观察到几乎没有基质相关离子的去质子分析物信号。使用 Box-Behnken 响应面设计并进行多响应优化,研究了最重要因素(激光能量、脉冲电压、DMAN/9AA 比、分析物/基质比)的影响,以同时最大化信噪比(S/N)和分辨率。通过 X 射线光电子能谱(XPS)探索了单或混合基质的化学表面组成。此外,XPS 成像用于绘制单或二元基质中模型磷脂的空间分布。然后成功地将 DMAN/9AA 二元基质应用于完整革兰氏阳性(旧金山乳杆菌)或革兰氏阴性(大肠杆菌)微生物的分析。在约 200 至约 1600 m/z 的质量范围内,快速且轻松地检测到约 50 种主要膜成分(游离脂肪酸、单、二和三甘油酯、磷脂、糖脂和心磷脂)。此外,与单基质相比,始终获得具有改善的 S/N 比(与单基质相比)、降低的化学噪声且没有形成基质簇的质谱,证明了这种二元基质提高灵敏度的潜力。