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自组装单层修饰硅基底以提高用于大气压基质辅助激光解吸电离质谱法的肽检测灵敏度。

Self-assembled-monolayer-modified silicon substrate to enhance the sensitivity of peptide detection for AP-MALDI mass spectrometry.

作者信息

Hsieh Shuchen, Ku Hsin-Yi, Ke Yao-Tang, Wu Hui-Fen

机构信息

Department of Chemistry and Center for Nanoscience and Nanotechnology, National Sun Yat-Sen University, 70 Lien-Hai Road, Kaohsiung, Taiwan 80424, Republic of China.

出版信息

J Mass Spectrom. 2007 Dec;42(12):1628-36. doi: 10.1002/jms.1261.

DOI:10.1002/jms.1261
PMID:17694592
Abstract

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.

摘要

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。

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