Direct analysis of biotransformations with mass spectrometry-DiBT-MS.

IF 13.1 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Ruth Knox, Rachel Smith, Emily E Kempa, Reynard Spiess, Christian Schnepel, Nicholas J Turner, Sabine L Flitsch, Perdita E Barran
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引用次数: 0

Abstract

The development and analysis of engineered enzymes is greatly assisted by the use of high-throughput screening to quickly determine the efficacy of biotransformations under various conditions. Ambient ionization, particularly desorption electrospray ionization (DESI), coupled to high-resolution mass spectrometry has the advantages of minimal requirements for sample preparation before analysis, which renders it suitable for high-throughput screening, in which the accurate mass and potentially the tandem mass spectrometry (MS) fingerprint for any given product can be used for identification. We present a protocol that permits the application of this method in routine biotechnology and chemical biology laboratories that are using engineered enzymes (such as imine reductases and carboxylic acid reductases, mentioned herein) to produce target compounds from substrates (quinoline moieties and phenyl(piperazinyl) moieties, respectively). Through the use of DESI's MS imaging capabilities, reaction monitoring can be easily visualized via imaging of selected substrate or product ions in a convenient, user-friendly workflow. We describe here how DESI-MS can be used to directly analyze the activity of biotransformations from crude cell lysate, which we term 'DiBT-MS'. The DiBT-MS method presented here is 10-1,000 times as fast as liquid chromatography-MS, with the full procedure for 96 samples taking ~2 h and consuming far less solvent and sample. Also demonstrated in this protocol is the impact of solvent spray composition on ionization efficiency of the target analyte, the benefits of a nylon membrane slide and the reusability of sample slides in multiple experiments.

质谱- dibt - ms直接分析生物转化。
利用高通量筛选快速确定各种条件下生物转化的功效,极大地辅助了工程酶的开发和分析。环境电离,特别是解吸电喷雾电离(DESI),与高分辨率质谱相结合,具有分析前对样品制备要求最低的优点,这使得它适用于高通量筛选,其中精确的质量和潜在的串联质谱(MS)指纹可用于任何给定产品的识别。我们提出了一种方案,允许在常规生物技术和化学生物学实验室中应用这种方法,这些实验室使用工程酶(如本文提到的亚胺还原酶和羧酸还原酶)从底物(分别为喹啉部分和苯基(哌嗪基)部分)产生目标化合物。通过使用DESI的MS成像功能,通过对选定的底物或产物离子进行成像,可以在方便、用户友好的工作流程中轻松可视化反应监测。我们在这里描述了如何使用DESI-MS直接分析粗细胞裂解物的生物转化活性,我们称之为“DiBT-MS”。本文提出的DiBT-MS方法比液相色谱- ms快10- 1000倍,96个样品的全部过程仅需2小时,并且消耗的溶剂和样品少得多。该方案还演示了溶剂喷雾成分对目标分析物电离效率的影响,尼龙膜载玻片的好处以及多次实验中样品载玻片的可重复使用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nature Protocols
Nature Protocols 生物-生化研究方法
CiteScore
29.10
自引率
0.70%
发文量
128
审稿时长
4 months
期刊介绍: Nature Protocols focuses on publishing protocols used to address significant biological and biomedical science research questions, including methods grounded in physics and chemistry with practical applications to biological problems. The journal caters to a primary audience of research scientists and, as such, exclusively publishes protocols with research applications. Protocols primarily aimed at influencing patient management and treatment decisions are not featured. The specific techniques covered encompass a wide range, including but not limited to: Biochemistry, Cell biology, Cell culture, Chemical modification, Computational biology, Developmental biology, Epigenomics, Genetic analysis, Genetic modification, Genomics, Imaging, Immunology, Isolation, purification, and separation, Lipidomics, Metabolomics, Microbiology, Model organisms, Nanotechnology, Neuroscience, Nucleic-acid-based molecular biology, Pharmacology, Plant biology, Protein analysis, Proteomics, Spectroscopy, Structural biology, Synthetic chemistry, Tissue culture, Toxicology, and Virology.
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