更便宜,更快,更简单的胰蛋白酶消化,用于高通量靶向蛋白质定量

IF 3.1 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Christopher M. Shuford, Russell P. Grant
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引用次数: 0

摘要

基于lc - ms的蛋白质定量方法具有相对昂贵和低通量的缺点。这部分是由于胰蛋白酶消化的成本和速度,主要集中在基于研究的生物标志物发现应用的进展,这些应用依赖于蛋白质/肽鉴定而不是临床生物标志物量化。然而,在临床生物标志物定量中,需要一种简单、快速、可重复高效的替代肽恢复方法。方法采用多种方法对甲状腺球蛋白(一种典型的血清蛋白生物标志物)进行胰消化分析。评估的主要标准是替代肽的产量和形成速度。除了消化时间外,各种因素,如不同的添加剂、胰蛋白酶类型、微波和压力辅助系统、酶浓度等都被认为是关键变量。结果消化添加剂/变性剂对各代肽的消化速度和产率有显著影响。发现单独增加胰蛋白酶的浓度可以明显地加速大多数替代肽的消化,而不影响产量。然而,一旦消化时间和添加剂得到优化,使用测序级胰蛋白酶和微波/压力辅助系统并不比使用“标准级”tpck处理胰蛋白酶与传统培养箱相结合具有显著优势。结论我们已经消除了胰蛋白酶消化固有的缓慢和昂贵的血清蛋白靶向定量的概念。此外,我们已经为实验奠定了基础,可以为创建高效胰蛋白酶消化方案铺平道路,旨在优化产量,速度和成本。我们希望这些进步将促进临床实验室更广泛地采用这种检测方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cheaper, faster, simpler trypsin digestion for high-throughput targeted protein quantification

Introduction

LC-MS-based methods for protein quantification have a stigma of being relatively expensive and low-throughput. This is partly due to the cost and speed of trypsin digestion, which has primarily focused on advancements in research-based biomarker discovery applications that rely on protein/peptide identifications rather than clinical biomarker quantification. However, there is a need for simple, fast, and reproducibly efficient surrogate peptide recovery in clinical biomarker quantification.

Methods

Multiple methodologies were evaluated to enhance tryptic digestion for the analysis of thyroglobulin, a prototypical serum protein biomarker. The main criteria for assessment were the yield and speed of formation of surrogate peptides. Various factors such as different additives, types of trypsin, microwave- and pressure-assisted systems, and enzyme concentration were considered as key variables, in addition to digestion time.

Results

It was observed that digestion additives/denaturants had a significant impact on the speed and yield of digestion for each surrogate peptide. Increasing the concentration of trypsin alone was found to accelerate digestions appreciably for most surrogate peptides, without affecting the yield. However, the use of sequencing-grade trypsins and microwave/pressure-assisted systems did not offer significant advantages over the use of 'standard-grade' TPCK-treated trypsin in combination with a conventional incubator, once digestion time and additive had been optimized.

Conclusion

We have dispelled the notion that trypsin digestion is inherently slow and expensive for targeted quantification of serum proteins. Additionally, we have established a groundwork for experimentation that can pave the way for the creation of efficient trypsin digestion protocols, aiming to optimize yield, speed, and cost. It is our hope that these advancements will promote the wider incorporation of such assays in clinical laboratories.

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来源期刊
Journal of Mass Spectrometry and Advances in the Clinical Lab
Journal of Mass Spectrometry and Advances in the Clinical Lab Health Professions-Medical Laboratory Technology
CiteScore
4.30
自引率
18.20%
发文量
41
审稿时长
81 days
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