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P物质相关肽的样品制备、高效液相色谱分离及测定

Sample preparation, high-performance liquid chromatographic separation and determination of substance P-related peptides.

作者信息

Rissler K

机构信息

Neurochemical Laboratory, University of Freiburg, Germany.

出版信息

J Chromatogr B Biomed Appl. 1995 Mar 24;665(2):233-70. doi: 10.1016/0378-4347(94)00533-b.

Abstract

This review deals with the determination of low levels of substance P and peptide fragments derived from the undecapeptide, i.e. covers the whole amount of so-called substance P-like immunoreactivity (SPLI) in biological samples. First an overview of the most currently used sample pretreatment procedures is given, followed by a description of the most effective high-performance liquid chromatographic (HPLC) separation methods. Special attention is paid to the choice of the appropriate column and the possible pitfalls encountered in separation of fmol amounts of peptide material. Subsequently the most important techniques of detection are discussed. This section primarily focuses on the coupling of HPLC with radioimmunoassay (RIA), which is indispensable for detection of components in the fmol range at present. Finally, some aspects of preparation and chromatographic separation of radiolabelled antigens for use in RIA are discussed.

摘要

本综述涉及低水平P物质及源自十一肽的肽片段的测定,即涵盖生物样品中所谓的P物质样免疫反应性(SPLI)的总量。首先概述了目前最常用的样品预处理程序,随后描述了最有效的高效液相色谱(HPLC)分离方法。特别关注了合适色谱柱的选择以及在分离飞摩尔量肽物质时可能遇到的陷阱。随后讨论了最重要的检测技术。本节主要关注HPLC与放射免疫分析(RIA)的联用,这对于目前飞摩尔范围内成分的检测不可或缺。最后,讨论了用于RIA的放射性标记抗原的制备和色谱分离的一些方面。

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