Cysteine-Functionalized Metal–Organic Framework: Facile Synthesis and High Efficient Enrichment of N‑Linked Glycopeptides in Cell Lysate

• Published in: ACS applied materials & interfaces Vol. 9; no. 23; pp. 19562 - 19568
• Main Authors: Ma, Wen, Xu, Linnan, Li, Xianjiang, Shen, Sensen, Wu, Mei, Bai, Yu, Liu, Huwei
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 14.06.2017
• Subjects: Cysteine; Glycopeptides; HeLa Cells; Humans; Hydrophobic and Hydrophilic Interactions; Metal-Organic Frameworks - chemistry; cell lysate; glycopeptide enrichment; mass spectrometry; metal−organic framework; fast functionalization
• ISSN: 1944-8244; 1944-8252
• DOI: 10.1021/acsami.7b02853

Cysteine-functionalized metal–organic framework (MOF) was synthesized via a common and facile two-step method of in situ loading of Au nanoparticles on amino-derived MOF followed by l-cysteine (Cys) immobilization. Owing to the large specific surface area and ultrahigh hydrophilicity of this nanocomposite, excellent performance was observed in the enrichment of N-linked glycopeptides in both model glycoprotein and HeLa cell lysate. By using this nanocomposite, 16 and 31 glycopeptides were efficiently extracted from digest of horseradish peroxidase (HRP) and human serum immunoglobulin G (IgG), respectively. The short incubation time (5 min), large binding capacity (150 mg/g, IgG digest to material), good selectivity (1:50, molar ratio of IgG and bovine serum albumin (BSA) digest), high recovery (over 80%), and low detection limit (1 fmol) ensure the effectiveness and robustness of MIL-101­(NH2)@Au-Cys in complex HeLa cell lysate. As a result, 1123 N-glycosylation sites corresponding to 1069 N-glycopeptides and 614 N-glycoproteins were identified from the lysate. Compared with those of previously reported hydrophilic methods, to our knowledge, it was the best result. This work paves a new way for fast functionalization of MOF and also provides a novel idea for material design in sample preparation, especially in glycoproteome and related analysis.