School of Materials Science and Chemical Engineering, Institute of Mass Spectrometry, Ningbo University, Ningbo, 315211, China.
Department of Thoracic Surgery, The First Affiliated Hospital of Ningbo University, No. 247 Renmin Road, Jiangbei District, Ningbo, 315020, China.
Anal Bioanal Chem. 2024 Aug;416(20):4491-4501. doi: 10.1007/s00216-024-05388-5. Epub 2024 Jun 14.
In the present study, click chemistry and Schiff base reactions were simultaneously applied to prepare polymer brush (PEG)-functionalized MOF materials (UiO-66-NH) and immobilized with Ti (MOF-Brush-THBA-Ti) for phosphopeptide analysis. The material has a detection limit of 0.5 fmol, a selectivity of 2000:1, and a loading capacity of 133 mg/g for phosphopeptides. It also demonstrated great repeatability (10 cycles) and recovery rate (96.7 ± 1.4%). During the analysis of bio-samples, 4 specific phosphopeptides were identified in endogenous breast cancer serum, while 11 phosphopeptides were identified in skimmed milk. Moreover, 47 phosphopeptides correlated with 29 phosphorylated proteins were selectively identified from normal control serum, and 66 phosphopeptides correlated with 26 phosphorylated proteins were identified from breast cancer serum. Further analysis of gene ontology (GO) revealed that the detected phosphorylated proteins associated with breast cancer included positive regulation of receptor-mediated endocytosis, proteolysis, extracellular exosome, heparin binding, and chaperone binding. These findings suggest that these associated pathways might contribute to the etiology of breast cancer. Overall, this application exhibits enormous potential in the identification of phosphorylated peptides within bio-samples.
在本研究中,点击化学和席夫碱反应同时被应用于制备聚合物刷(PEG)功能化的 MOF 材料(UiO-66-NH),并通过 Ti(MOF-Brush-THBA-Ti)固定化用于磷酸肽分析。该材料对磷酸肽的检测限为 0.5 fmol,选择性为 2000:1,负载量为 133 mg/g。它还表现出良好的重复性(10 个循环)和回收率(96.7±1.4%)。在生物样本分析中,在内源性乳腺癌血清中鉴定出 4 种特定的磷酸肽,而在脱脂乳中鉴定出 11 种磷酸肽。此外,从正常对照血清中选择性地鉴定出与 29 种磷酸化蛋白相关的 47 种磷酸肽,从乳腺癌血清中鉴定出与 26 种磷酸化蛋白相关的 66 种磷酸肽。进一步的基因本体(GO)分析表明,检测到的与乳腺癌相关的磷酸化蛋白与受体介导的内吞作用、蛋白水解、细胞外外泌体、肝素结合和伴侣结合的正调控有关。这些发现表明,这些相关途径可能有助于乳腺癌的发病机制。总的来说,这项应用在生物样本中鉴定磷酸肽方面具有巨大的潜力。