4.6 Article

Design of two-dimensional molybdenum trioxide-immobilized magnetic graphite nitride nanocomposites with multiple affinity sites for phosphopeptide enrichment

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1678, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2022.463374

Keywords

Graphite nitride; Molybdenum trioxide; Magnetic; Nanocomposite; Phosphopeptide enrichment

Funding

  1. National Natural Science Foundation of China [22004073, 21961024, 21961025]
  2. Natural Science Foundation of Inner Mongolia [2020BS02010]
  3. Talent Research Support Funds from Government-Sponsored Institution of Inner Mongolia [RCQD19002]
  4. Inner Mongolia Minzu University Doctoral Research Startup Fund Project [BS516]
  5. Nano Innovation Institute (NII) of Inner Mongolia Minzu University

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In this study, two-dimensional magnetic graphite nitride nanosheets were synthesized and distributed with molybdenum trioxide. The magnetic nanocomposite exhibited high selectivity, sensitivity, quantitative recovery, and recyclability for phosphopeptide enrichment. It also showed excellent performance in enriching phosphopeptides from various samples, highlighting its significance in phosphorylated proteomics.
Here, two-dimensional magnetic graphite nitride nanosheets were synthesized, over which molybdenum trioxide was distributed evenly. The magnetic nanocomposite served as an enrichment platform for phosphopeptides based on metal oxide affinity chromatography and anion-exchange chromatography. Owing to the abundant affinity sites, positive electricity, and large surface area, the nanocomposite had high selectivity (alpha-casein/beta-casein/bovine serum albumin, 1:1:5000), sensitivity (0.1 fmol), quantitative recovery (91.3%), and good recyclability (10 cycles). The nanocomposite also showed good enrichment performance for phosphopeptides from non-fat milk, human serum, saliva, and A549 cell lysate. The results demonstrated the value of this material in phosphorylated proteomics. (C) 2022 Elsevier B.V. All rights reserved.

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