Peng Jianhe, Stanley Anthea J, Cairns David, Selby Peter J, Banks Rosamonde E
Cancer Research UK Clinical Centre, St James's University Hospital, Leeds, UK.
Proteomics. 2009 Jan;9(2):492-8. doi: 10.1002/pmic.200800424.
Mass spectrometric profiling, particularly in the form of SELDI, has been used in many studies, particularly in attempts to generate diagnostic serum profiles. Several studies have generated promising results but one of the limitations is the inability to identify easily potential discriminatory peaks. This may enable specific assays to be developed and increased biological insight. We describe the first systematic technical evaluation of the ProteinChip interface coupled to a tandem mass spectrometer which allows direct sequencing of peptides <6000 Da, and describe the direct sequence identification of 21 peaks commonly observed in serum samples. Additionally we describe for the first time the use of on-chip acetylation to assist in the validation of sequence identification.
质谱分析,尤其是表面增强激光解吸电离(SELDI)形式的质谱分析,已在许多研究中得到应用,特别是在尝试生成诊断血清图谱方面。一些研究已取得了有前景的结果,但其中一个局限性是难以轻松识别潜在的鉴别峰。这可能有助于开发特定检测方法并增进生物学理解。我们描述了与串联质谱仪联用的蛋白质芯片接口的首次系统技术评估,该接口可对分子量小于6000道尔顿的肽段进行直接测序,并描述了血清样本中常见的21个峰的直接序列鉴定。此外,我们首次描述了使用芯片上乙酰化来辅助序列鉴定的验证。