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Minimizing Postsampling Degradation of Peptides by a Thermal Benchtop Tissue Stabilization Method

机译:通过热台式组织稳定化方法使肽的后采样降解最小化

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Enzymatic degradation is a major concern in peptide analysis. Postmortem metabolism in biological samples entails considerable risk for measurements misrepresentative of true in vivo concentrations. It is therefore vital to find reliable, reproducible, and easy-to-use procedures to inhibit enzymatic activity in fresh tissues before subjecting them to qualitative and quantitative analyses. The aim of this study was to test a benchtop thermal stabilization method to optimize measurement of endogenous opioids in brain tissue. Endogenous opioid peptides are generated from precursor proteins through multiple enzymatic steps that include conversion of one bioactive peptide to another, often with a different function. Ex vivo metabolism may, therefore, lead to erroneous functional interpretations. The efficacy of heat stabilization was systematically evaluated in a number of postmortem handling procedures. Dynorphin B (DYNB), Leu-enkephalin-Arg(6) (LARG), and Met-enkephalin-Arg(6)-Phe(7) (MEAP) were measured by radioimmunoassay in rat hypothalamus, striatum (STR), and cingulate cortex (CCX). Also, simplified extraction protocols for stabilized tissue were tested. Stabilization affected all peptide levels to varying degrees compared to those prepared by standard dissection and tissue handling procedures. Stabilization increased DYNB in hypothalamus, but not STR or CCX, whereas LARG generally decreased. MEAP increased in hypothalamus after all stabilization procedures, whereas for STR and CCX, the effect was dependent on the time point for stabilization. The efficacy of stabilization allowed samples to be left for 2 hours in room temperature (20 degrees C) without changes in peptide levels. This study shows that conductive heat transfer is an easy-to-use and efficient procedure for the preservation of the molecular composition in biological samples. Region- and peptide-specific critical steps were identified and stabilization enabled the optimization of tissue handling and opioid peptide analysis. The result is improved diagnostic and research value of the samples with great benefits for basic research and clinical work.
机译:酶促降解是肽分析中的主要问题。生物样品中的事后代谢会带来相当大的风险,导致测量结果不能正确代表真实的体内浓度。因此,在对新鲜组织进行定性和定量分析之前,找到可靠,可重现和易于使用的程序来抑制酶的活性至关重要。这项研究的目的是测试一种台式热稳定方法,以优化大脑组织中内源性阿片样物质的测量。内源性阿片肽是通过多种酶促步骤从前体蛋白中产生的,这些步骤包括将一种生物活性肽转换为另一种通常具有不同功能的肽。因此,离体代谢可能导致错误的功能解释。在许多事后处理程序中,系统地评估了热稳定的功效。用放射免疫法测定大鼠下丘脑,纹状体和扣带中的强啡肽B(DYNB),亮脑啡肽-Arg(6)(LARG)和蛋氨酸脑啡肽-Arg(6)-Phe(7)(MEAP)。皮质(CCX)。此外,测试了用于稳定组织的简化提取方案。与通过标准解剖和组织处理程序制备的肽相比,稳定作用在不同程度上影响了所有肽水平。稳定增加下丘脑的DYNB,但不增加STR或CCX,而LAR​​G通常减少。在所有稳定程序后,下丘脑的MEAP增加,而对于STR和CCX,效果取决于稳定的时间点。稳定的功效使样品在室温(20摄氏度)下放置2小时,而肽水平没有变化。这项研究表明,传导热传递是一种易于使用且有效的程序,可用于保存生物样品中的分子成分。确定了区域和肽特定的关键步骤,稳定化使得组织处理和阿片类肽分析的优化成为可能。结果提高了样品的诊断和研究价值,对基础研究和临床工作大有裨益。

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