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使用精确质量和洗脱时间肽标签结合毛细管液相色谱飞行时间质谱法进行蛋白质组分析。

Proteome analyses using accurate mass and elution time peptide tags with capillary LC time-of-flight mass spectrometry.

作者信息

Strittmatter Eric F, Ferguson P Lee, Tang Keqi, Smith Richard D

机构信息

Environmental and Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.

出版信息

J Am Soc Mass Spectrom. 2003 Sep;14(9):980-91. doi: 10.1016/S1044-0305(03)00146-6.

Abstract

We describe the application of capillary liquid chromatography (LC) time-of-flight (TOF) mass spectrometric instrumentation for the rapid characterization of microbial proteomes. Previously (Lipton et al., Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 11049) the peptides from a series of growth conditions of Deinococcus radiodurans have been characterized using capillary LC MS/MS and accurate mass measurements which are captured as an accurate mass and time (AMT) tag database. Using this AMT tag database, detected peptides can be assigned using measurements obtained on a TOF due to the additional use of elution time data as a constraint. When peptide matches are obtained using AMT tags (i.e., using both constraints) unique matches of a mass spectral peak occurs 88% of the time. Not only are AMT tag matches unique in most cases, the coverage of the proteome is high; approximately 3500 unique peptide AMT tags are found on average per capillary LC run. From the results of the AMT tag database search, approximately 900 ORFs detected using LC-TOFMS, with approximately 500 ORFs covered by at least two AMT tags. These results indicate that AMT database searches with modest mass and elution time criteria can provide proteomic information for approximately one thousand proteins in a single run of <3 h. The advantage of this method over using MS/MS based techniques is the large number of identifications that occur in a single experiment as well as the basis for improved quantitation. For MS/MS experiments, the number of peptide identifications is severely restricted because of the time required to dissociate the peptides individually. These results demonstrate the utility of the AMT tag approach using capillary LC-TOF MS instruments, and also show that AMT tags developed using other instrumentation can be effectively utilized.

摘要

我们描述了毛细管液相色谱(LC)飞行时间(TOF)质谱仪器在快速表征微生物蛋白质组中的应用。此前(Lipton等人,《美国国家科学院院刊》2002年,99卷,11049页),已使用毛细管LC MS/MS和精确质量测量对耐辐射球菌一系列生长条件下的肽段进行了表征,这些测量结果被捕获为精确质量和时间(AMT)标签数据库。利用这个AMT标签数据库,由于额外使用洗脱时间数据作为约束条件,因此可以根据在TOF上获得的测量结果来指定检测到的肽段。当使用AMT标签获得肽段匹配结果时(即使用两个约束条件),质谱峰的唯一匹配在88%的时间内出现。AMT标签匹配不仅在大多数情况下是唯一的,而且蛋白质组的覆盖率很高;每次毛细管LC运行平均可发现约3500个独特的肽段AMT标签。根据AMT标签数据库搜索结果,使用LC-TOFMS检测到约900个开放阅读框(ORF),其中约500个ORF至少被两个AMT标签覆盖。这些结果表明,使用适度的质量和洗脱时间标准进行AMT数据库搜索,在单次<3小时的运行中可为大约一千种蛋白质提供蛋白质组信息。与使用基于MS/MS的技术相比,该方法的优势在于单次实验中出现的大量鉴定结果以及改进定量的基础。对于MS/MS实验,由于需要分别解离肽段,肽段鉴定的数量受到严重限制。这些结果证明了使用毛细管LC-TOF MS仪器的AMT标签方法的实用性,也表明使用其他仪器开发的AMT标签可以得到有效利用。

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