MUSC Proteomics Center, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Anal Chem. 2010 Sep 15;82(18):7772-8. doi: 10.1021/ac1017277.
A novel matrix-free LDI MS platform using a thin film of patterned nanostructured gold, capped with methyl- and carboxy-terminated self-assembled monolayers (SAMs) is presented. Calibration on the matrix-free LDI surface was performed using a peptide standard mixture available for MALDI analysis. MS analysis for limit of detection was performed using angiotensin I peptide. Peptide fragments from standard protein digests of bovine serum albumin, bovine catalase, and bovine lactoperoxidase were used to carry out peptide mass fingerprinting analysis. Sequence coverage of each protein digest and the number of detected peptide fragments were compared with conventional MALDI MS on a standard MALDI plate. Versatility of the nanostructured gold LDI substrate is illustrated by performing MS analysis on a protein digest using different enzymes and by small molecule MS analysis.
一种新型无基质 LDI MS 平台,使用带有图案纳米结构金薄膜,并覆盖甲基和羧基封端的自组装单层(SAMs)。在无基质 LDI 表面进行了使用 MALDI 分析可用的肽标准混合物的校准。使用血管紧张素 I 肽进行了用于检测限的 MS 分析。使用牛血清白蛋白、牛过氧化氢酶和牛乳过氧化物酶的标准蛋白消化物中的肽片段进行肽质量指纹图谱分析。与标准 MALDI 板上的常规 MALDI MS 相比,比较了每个蛋白消化物的序列覆盖率和检测到的肽片段数量。通过使用不同的酶进行蛋白消化物的 MS 分析以及小分子 MS 分析,说明了纳米结构金 LDI 底物的多功能性。