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利用基质辅助激光解吸/电离飞行时间/飞行时间质谱直接对来自猪蛔虫组织的新型神经肽进行从头测序。

De novo sequencing of novel neuropeptides directly from Ascaris suum tissue using matrix-assisted laser desorption/ionization time-of-flight/time-of-flight.

作者信息

Yew Joanne Y, Dikler Sergei, Stretton Antony O

机构信息

Neuroscience Training Program and Department of Zoology, 1117 West Johnson St., Madison, WI 53706, USA.

出版信息

Rapid Commun Mass Spectrom. 2003;17(24):2693-8. doi: 10.1002/rcm.1240.

Abstract

Direct analysis of tissue by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) allows for the rapid profiling of biological molecules with minimal loss of sample or degradation and reduced likelihood of chemical modification. However, there are still considerable challenges to overcome due to the complexity of tissue and the low quantity of endogenous peptide in a single cell. These problems are exacerbated in the nematode Ascaris suum because of the small size of individual neurons and the paucity of peptide per cell. In an effort to address these difficulties, the recently developed matrix-assisted laser desorption/ionization time-of-flight/time-of-flight (MALDI-TOF/TOF) technology was used in combination with an on-target derivatization in order to sequence novel neuropeptides directly from Ascaris nervous tissue. Direct MALDI-TOF/TOF analysis of Ascaris tissue provided the complete amino acid sequences for a previously characterized neuropeptide as well as for three novel peptides with homologues found in other nematodes. These results demonstrate a method for the rapid characterization of sub-femtomolar amounts of peptide directly from tissue using MALDI-TOF/TOF.

摘要

通过基质辅助激光解吸/电离质谱(MALDI-MS)对组织进行直接分析,能够在样品损失或降解最小且化学修饰可能性降低的情况下,快速分析生物分子。然而,由于组织的复杂性以及单个细胞中内源性肽的含量较低,仍有相当多的挑战需要克服。在猪蛔虫中,由于单个神经元体积小且每个细胞中的肽含量稀少,这些问题更加突出。为了解决这些困难,最近开发的基质辅助激光解吸/电离飞行时间/飞行时间(MALDI-TOF/TOF)技术与靶上衍生化相结合,以便直接从蛔虫神经组织中对新型神经肽进行测序。对蛔虫组织进行直接MALDI-TOF/TOF分析,得到了一种先前已鉴定的神经肽以及三种在其他线虫中发现有同源物的新型肽的完整氨基酸序列。这些结果证明了一种使用MALDI-TOF/TOF直接从组织中快速鉴定亚飞摩尔量肽的方法。

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