Highly Selective and Large Scale Mass Spectrometric Analysis of 4-Hydroxynonenal Modification via Fluorous Derivatization and Fluorous Solid-Phase Extraction-Reference-Cited by-全球学者库

Highly Selective and Large Scale Mass Spectrometric Analysis of 4-Hydroxynonenal Modification via Fluorous Derivatization and Fluorous Solid-Phase Extraction

Published:2017-02-13 Issue:5 Volume:89 Page:3093-3100
ISSN:0003-2700
Container-title:Analytical Chemistry
language:en
Short-container-title:Anal. Chem.

Author:

Yuan Wenjuan¹²,Zhang Ying¹,Xiong Yun¹,Tao Tao¹²,Wang Yi¹,Yao Jun¹,Zhang Lei¹,Yan Guoquan²,Bao Huimin²,Lu Haojie¹²³^ORCID

Affiliation:

1. Shanghai Cancer Center and Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, P. R. China

2. Department of Chemistry, Fudan University, Shanghai 200433, P. R. China

3. Key Laboratory of Glycoconjugates Research Ministry of Public Health, Fudan University, Shanghai 200032, P. R. China

Funder

Ministry of Education of the People's Republic of China

Ministry of Science and Technology of the People's Republic of China

National Science Foundation

Shanghai Key Laboratory of Clinical Geriatric Medicine and Shanghai Projects

Publisher

American Chemical Society (ACS)

Subject

Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.analchem.6b04850

Reference37 articles.

1. Cytotoxicity and genotoxicity of lipid-oxidation products

2. Temporally Controlled Targeting of 4-Hydroxynonenal to Specific Proteins in Living Cells

3. Enhanced glutathione depletion, protein adduct formation, and cytotoxicity following exposure to 4-hydroxy-2-nonenal (HNE) in cells expressing human multidrug resistance protein-1 (MRP1) together with human glutathione S-transferase-M1 (GSTM1)

4. Structural proteomics of macromolecular assemblies using oxidative footprinting and mass spectrometry

5. Characterization of 4-Hydroxy-2-nonenal-Modified Peptides by Liquid Chromatography−Tandem Mass Spectrometry Using Data-Dependent Acquisition: Neutral Loss-Driven MS3 versus Neutral Loss-Driven Electron Capture Dissociation

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