In situ digestion-assisted multi-template imprinted nanoparticles for efficient analysis of protein phosphorylation

• Published in: Mikrochimica acta (1966) Vol. 190; no. 12; p. 490
• Main Authors: Wang, Jie, Zhao, Xiuling, Zhang, Hui, Chen, Yang, Bie, Zijun
• Format: Journal Article
• Language: English
• Published: Vienna Springer Vienna 01.12.2023; Springer Nature B.V
• Subjects: Analytical Chemistry; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Controllability; Digestion; Microengineering; Nanochemistry; Nanoparticles; Nanotechnology; Original Paper; Peptides; Phosphorylation; Proteomics; Nanoparticles; Phosphopeptides; Affinity separation; Molecule imprinting; Protein phosphorylation
• ISSN: 0026-3672; 1436-5073
• DOI: 10.1007/s00604-023-06081-7

A new general approach called in situ digestion-assisted multi-template imprinting is proposed for preparation of phospho-specific molecularly imprinted nanoparticles. Through the novel templating strategy and controllable imprinting process, imprinted nanoparticles specific to the intact phosphoprotein and its phosphopeptides were synthesized. The prepared imprinted nanoparticles exhibited excellent specificity (cross reactivity < 10%), high affinity (10 −6  M), high efficiency (47.5%), and good generality (both intact phosphoprotein and phosphopeptides). We also realized the fine tuning of the recognition at peptide level of the imprinted nanoparticles by adjusting the imprinting time. Based on the selective enrichment of the imprinted nanoparticles, the MS identification of both the intact phosphoprotein (Tau) and phosphopeptides (angiotensin II and peptides of Tau) in real complex samples could be achieved. Therefore, we believe that the in situ digestion-assisted multi-template imprinting strategy holds promising future in both phosphorylation analysis and proteomics applications. Graphical abstract