Haskins William E, Watson Christopher J, Cellar Nicholas A, Powell David H, Kennedy Robert T
Department of Chemistry, University of Florida, Gainesville, Florida 32611, USA.
Anal Chem. 2004 Sep 15;76(18):5523-33. doi: 10.1021/ac049363y.
Endogenous peptides from brain extracellular fluid of live rats were analyzed using capillary liquid chromatography (LC)-tandem mass spectrometry (MS2). A 4-mm-long microdialysis probe perfused at 0.6 microL/min implanted into the striatum of anesthetized male rats was used to collect 3.6 microL dialysate fractions that were injected on-line into the capillary LC-MS2 system for analysis. A total of 3349 MS2 spectra were collected from 13 different animals under basal conditions and during localized depolarization evoked by infusion of a high-K+ solution through the microdialysis probe. Subtractive analysis revealed a total of 859 MS2 spectra that were observed only during depolarization. From these spectra, 29 peptide sequences (25 were peptides not previously observed) from 6 different protein precursors were identified using database searching software. Proteins identified include precursors to neuropeptides, synaptic proteins, blood proteins, and transporters. The identified peptides represent candidates for neurotransmitters, neuromodulators, and markers of synaptic activity or brain tissue damage. A screen for neuroactivity of novel proenkephalin fragments that were found was performed by infusing the peptides into the brain while monitoring amino acid neurotransmitters by microdialysis sampling combined with capillary electrophoresis. Three of the six tested peptides evoked significant increases in various neuroactive amino acids. These results demonstrate that this combination of methods can identify novel neurotransmitter candidates and screen for potential neuroactivity.
采用毛细管液相色谱(LC)-串联质谱(MS2)分析法对活大鼠脑细胞外液中的内源性肽进行分析。将一根4毫米长的微透析探针以0.6微升/分钟的速度灌注,植入麻醉的雄性大鼠纹状体中,用于收集3.6微升透析液馏分,这些馏分在线注入毛细管LC-MS2系统进行分析。在基础条件下以及通过微透析探针注入高钾溶液诱发局部去极化期间,从13只不同的动物身上总共收集了3349个MS2光谱。减法分析显示,总共859个MS2光谱仅在去极化期间观察到。利用数据库搜索软件从这些光谱中鉴定出了来自6种不同蛋白质前体的29个肽序列(25个是以前未观察到的肽)。鉴定出的蛋白质包括神经肽前体、突触蛋白、血液蛋白和转运蛋白。鉴定出的肽代表神经递质、神经调质以及突触活动或脑组织损伤标志物的候选物。通过将发现的新型脑啡肽原片段注入大脑,同时通过微透析采样结合毛细管电泳监测氨基酸神经递质,对其神经活性进行筛选。六个测试肽中的三个在各种神经活性氨基酸中引起了显著增加。这些结果表明,这种方法组合可以鉴定新型神经递质候选物并筛选潜在的神经活性。