Hsieh Shuchen, Ku Hsin-Yi, Ke Yao-Tang, Wu Hui-Fen
Department of Chemistry and Center for Nanoscience and Nanotechnology, National Sun Yat-Sen University, 70 Lien-Hai Road, Kaohsiung, Taiwan 80424, Republic of China.
J Mass Spectrom. 2007 Dec;42(12):1628-36. doi: 10.1002/jms.1261.
A self-assembled-monolayer-modified silicon substrate was successfully used to enhance the sensitivity of peptide detection for atmospheric pressure-matrix-assisted laser desorption/ionization mass spectrometry (AP-MALDI/MS). The effect of surface modification of silicon wafer samples with NH(2) and OH functional groups was investigated. In addition, solvent effects for the preparation of modified NH(2)-functionalized surfaces were examined. The sensitivities for the two peptides were significantly improved, increasing between 12 and 160 times, for bradykinin and gramicidin, respectively, on an NH(2)-modified silicon surface prepared in toluene, over that on a conventional gold substrate. The limits of detection (LODs) for bradykinin and gramicidin using the conventional gold substrate in AP-MALDI/MS experiments were > 0.011 microM and 110 microM, respectively. Using our SAM approach, the LODs for bradykinin and gramicidin in AP-MALDI/MS can be improved to 0.93 nM and 0.33 microM, respectively. This SAM approach for AP-MALDI/MS is simple and sensitive, and can be used for high-throughput analysis.
自组装单层修饰的硅基底成功用于提高大气压基质辅助激光解吸/电离质谱(AP-MALDI/MS)中肽检测的灵敏度。研究了用NH(2)和OH官能团对硅片样品进行表面修饰的效果。此外,还考察了制备修饰的NH(2)官能化表面时的溶剂效应。在甲苯中制备的NH(2)修饰硅表面上,两种肽的灵敏度显著提高,缓激肽和短杆菌肽的灵敏度分别比传统金基底提高了12至160倍。在AP-MALDI/MS实验中,使用传统金基底时缓激肽和短杆菌肽的检测限(LOD)分别>0.011 microM和110 microM。使用我们的自组装单层方法,AP-MALDI/MS中缓激肽和短杆菌肽的LOD可分别提高到0.93 nM和0.33 microM。这种用于AP-MALDI/MS的自组装单层方法简单且灵敏,可用于高通量分析。