Bioinspired dandelion-like silica nanoparticles modified with L-glutathione for highly efficient enrichment of N-glycopeptides in biological samples
Creators
- 1. CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023 (China)
- 2. College of Chemistry and Chemical Engineering, North Minzu University, Yinchuan, 750021 (China)
- 3. University of Chinese Academy of Sciences, Beijing, 100049 (China)
Description
Highlights: • A simple "one-pot" strategy was presented to prepare bioinspired dandelion-like silica nanoparticles. • After hydrophilic modification, these nanoparticles could be used as HILIC sorbents for enriching N-glycopeptides. • Up to 594 unique N-glycopeptides from 182 N-glycoproteins were identified from 2 μL of human serum digest. The pretreatment of complicated biological samples to eliminate the interference of nonglycopeptides and improve the efficiency of glycopeptides detection is crucial in glycoproteomics research. Hydrophilic interaction chromatography (HILIC) has been adopted for enrichment of glycosylated peptides following identification with mass spectrometry, but it is still urgent to develop novel hydrophilic materials to save cost and improve enrichment efficiency. Scientists are pursuing to fabricate freestanding intelligent artificial materials. One promising approach is to use biomimic material. In our case, "one-pot" strategy was developed to prepare bioinspired nano-core-shell silica microspheres (CSSMs), employing tetrapropylorthosilicate as the silicon source and phenolic resin as the soft template. The pore structure of the obtained microspheres diverged from the center to the outside with diameter ranged from 150 to 340 nm, and shell layer ranged from 25 to 83 nm by adjusting the preparation parameters. Some of them showed dandelion-like morphology. After hydrophilic modification, these CSSMs exhibited great hydrophilicity and could be used as sorbents for enriching N-glycopeptides from complicated biological samples in HILIC. Up to 594 unique N-glycopeptides and 367 N-glycosylation sites from 182 N-glycoproteins were unambiguously identified from 2 μL of human serum, which was superior to the enrichment performance of many HILIC materials in reported papers, demonstrating great potential advantages in proteomic application.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.aca.2021.338694Additional details
Identifiers
- DOI
- 10.1016/j.aca.2021.338694;
- PII
- S0003267021005201;
Publishing Information
- Journal Title
- Analytica Chimica Acta
- Journal Volume
- 1173
- Journal Page Range
- vp.
- ISSN
- 0003-2670
- CODEN
- ACACAM
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53096750
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- EFFICIENCY; GLUTATHIONE; GLYCOPROTEINS; LAYERS; MASS SPECTROSCOPY; NANOPARTICLES; PERFORMANCE; PHENOLS; PORE STRUCTURE; POTENTIALS; SILICA; SILICON
- Descriptors DEC
- AROMATICS; CARBOHYDRATES; DRUGS; ELEMENTS; HYDROCARBONS; HYDROXY COMPOUNDS; MICROSTRUCTURE; MINERALS; ORGANIC COMPOUNDS; OXIDE MINERALS; PARTICLES; PEPTIDES; POLYPEPTIDES; PROTEINS; RADIOPROTECTIVE SUBSTANCES; RESPONSE MODIFYING FACTORS; SACCHARIDES; SEMIMETALS; SPECTROSCOPY
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.