Strategies for large-scale targeted metabolomics quantification by liquid chromatography-mass spectrometry
文献情報
Juntuo Zhou, Yuxin Yin
Advances in liquid chromatography-mass spectrometry (LC-MS) instruments and analytical strategies have brought about great progress in targeted metabolomics analysis. This methodology is now capable of performing precise targeted measurement of dozens or hundreds of metabolites in complex biological samples. Classic targeted quantification assay using the multiple reaction monitoring (MRM) mode has been the foundation of high-quality metabolite quantitation. However, utilization of this strategy in biological studies has been limited by its relatively low metabolite coverage and throughput capacity. A number of methods for large-scale targeted metabolomics assay which have been developed overcome these limitations. These strategies have enabled extended metabolite coverage which is defined as targeting of large numbers of metabolites, while maintaining reliable quantification performance. These recently developed techniques thus bridge the gap between traditional targeted metabolite quantification and untargeted metabolomics profiling, and have proven to be powerful tools for metabolomics study. Although the LC-MRM-MS strategy has been used widely in large-scale metabolomics quantification analysis due to its fast scan speed and ideal analytic stability, there are still drawbacks which are due to the low resolution of the triple quadrupole instruments used for MRM assays. New approaches have been developed to expand the options for large-scale targeted metabolomics study, using high-resolution instruments such as parallel reaction monitoring (PRM). MRM and PRM-based techniques are now attractive strategies for quantitative metabolomics analysis and high-throughput biomarker discovery. Here we provide an overview of the major developments in LC-MS-based strategies for large-scale targeted metabolomics quantification in biological samples. The advantages of LC-MRM/PRM-MS based analytical strategies which may be used in multiplexed and high throughput quantitation for a wide range of metabolites are highlighted. In particular, PRM and MRM strategies are compared, and we summarize the work flow commonly used for large-scale targeted metabolomics analysis including sample preparation, LC separation and data analysis, as well as recent applications in biological studies.
関連文献
Tunable band gaps and high carrier mobilities in stanene by small organic molecule adsorption under external electric fields
Mei-Xia Xiao, Xiao Shao, Hai-Yang Song, Zhao Li, Min-Rong An, Cheng He
DOI: 10.1039/D1CP01582F
Ambiguities in solvation free energies from cluster-continuum quasichemical theory: lithium cation in protic and aprotic solvents
Luigi Cavallo
DOI: 10.1039/D1CP01454D
Electrically tunable band gap in strained h-BN/silicene van der Waals heterostructures
Douglas D. de Vargas, Rogério J. Baierle
DOI: 10.1039/D1CP02012A
New ethionamide boosters and EthR2: structural and energetic analysis
J. F. Vianna, K. S. Bezerra, A. H. Lima Costa, E. D. Barbosa, J. X. Lima Neto, J. I. N. Oliveira, V. N. Freire, U. L. Fulco
DOI: 10.1039/D1CP02853G
The CH(X2Π) + H2O reaction: two transition state kinetics
Thanh Lam Nguyen, Jozef Peeters
DOI: 10.1039/D1CP02234B
Large Rashba splitting, carrier mobility, and valley polarization in a 1T-SnS2/MoTe2 heterostructure
Sukai Teng, Jia Li, Xiujuan Mao, Fuli He, Ze Liu, Jiaxi Wang, Yafan Wang
DOI: 10.1039/D1CP02039K
Assessing nickel oxide electrocatalysts incorporating diamines and having improved oxygen evolution activity using operando UV/visible and X-ray absorption spectroscopy
Takafumi Miura, Shun Tsunekawa, Sho Onishi, Toshiaki Ina, Kehsuan Wang, Genta Watanabe, Chechia Hu, Hiroshi Kondoh, Takeshi Kawai
DOI: 10.1039/D1CP03323A
Molecular dynamics study on the inhibition mechanisms of ReACp53 peptide for p53–R175H mutant aggregation
Jiangtao Lei, Mengqiang Cai, Yun Shen, Dongdong Lin, Xiaohua Deng
DOI: 10.1039/D1CP03094A
Tuning Dzyaloshinskii–Moriya interaction via an electric field at the Co/h-BN interface
C. L. Ma, J. Hu
DOI: 10.1039/D1CP02554F
The disparate effect of strain on thermal conductivity of 2-D materials
K. V. S. Dheeraj, Sarith P. Sathian
DOI: 10.1039/D1CP02771A
こちらもおすすめ
4-アミノフェノール酸ナトリウム水和物とは何ですか?
4-アミノフェノール酸ナトリウム水和物は、CAS番号206557-08-6の化合物で、4-アミノフェノールとナトリウムが結合した塩と水和物です。この化合物は、白...
Methyl 3-methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-histidinateの代替品はありますか?
この化合物は特定の合成プロセスに使用される可能性がありますが、代替品として、他の类似的な化合物、例えばMethyl 3-methyl-N-{[(2-methyl...
4-Boc-2-哌嗪甲酸の市場動向や研究トレンドはどうですか?
4-Boc-2-哌嗪甲酸は、薬品開発や合成化学分野で広く使用されており、その需要は継続的に推移しています。特に、新薬開発における合成化学分野での需要が高まってい...
4,4'-二羟甲基联苯の物理化学的性質は何ですか?
4,4'-二羟甲基联苯のCAS番号は1667-12-5です。この化合物は白色の結晶粉末で、分子量は154.20です。水にわずかに溶けますが、アルコールや有機溶媒...
5-甲硫基戊腈はどの業界で使用されていますか?
5-甲硫基戊腈は医薬品産業で使用される可能性があります。また、ポリマー合成の触媒として、センサー製造の一部として、半導体製造のプロセス改善に使用される可能性があ...
CAS番号1311961-50-8の化合物はどのように合成されますか?
この化合物は、1-abieta-8,11,13-trien-19-イルと6'-メトキシシンコナナン-9-基を含有する窒素含有化合物から合成されます。一般的な合成...
6-ブロモベンジジミダゾール-2-カルビルデオキシドはどのように保存すればよいですか?
6-ブロモベンジジミダゾール-2-カルビルデオキシドは、避光・乾燥した容器(密閉容器)で-20℃~4℃の低温で保存してください。高温や直射日光、湿気は避けてくだ...
Boc-N-甲基氨甲环酸とは何ですか?
621-65-8のCAS番号を持つBoc-N-甲基氨甲环酸は、化学式C7H13NO5を有する化合物です。この化合物は白色の結晶性粉末で、吸湿性があります。
乙基三氟硼酸钾はどのように合成されますか?
乙基三氟硼酸钾は、トリフLUオール酸カリウムとエチルブロミドを反応させて合成されます。この反応は高い選択性と収率を持ち、触媒を用いることで効率的に進行します。
2-フロウロ-5-クロロ-4-アミノフェノールはどのように保存すればよいですか?
2-フロウロ-5-クロロ-4-アミノフェノールは、直射日光を避けて冷却された暗所で保存し、密閉容器に保管してください。温度は常温か低温が適しています。
掲載誌
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.














