Key Laboratory of Synthetic and Natural Function Molecule Chemistry of Ministry of Education, College of Chemistry and Materials Science , Northwest University , Xi'an 710069 , China.
State Key Laboratory of Proteomics, National Center for Protein Science Beijing , Beijing Institute of Life-omics , Beijing 102206 , China.
Anal Chem. 2018 Jun 5;90(11):6651-6659. doi: 10.1021/acs.analchem.8b00461. Epub 2018 May 17.
Mass spectrometry (MS)-based glycoproteomics research requires highly efficient sample preparation to eliminate interference from non-glycopeptides and to improve the efficiency of glycopeptide detection. In this work, a novel MoS/Au-NP (gold nanoparticle)-L-cysteine nanocomposite was prepared for glycopeptide enrichment. The two-dimensional (2D) structured MoS nanosheets served as a matrix that could provide a large surface area for immobilizing hydrophilic groups (such as L-cysteine) with low steric hindrance between the materials and the glycopeptides. As a result, the novel nanomaterial possessed an excellent ability to capture glycopeptides. Compared to commercial zwitterionic hydrophilic interaction liquid chromatography (ZIC-HILIC) materials, the novel nanomaterials exhibited excellent enrichment performance with ultrahigh selectivity and sensitivity (approximately 10 fmol), high binding capacity (120 mg g), high enrichment recovery (more than 93%), satisfying batch-to-batch reproducibility, and good universality for glycopeptide enrichment. In addition, its outstanding specificity and efficiency for glycopeptide enrichment was confirmed by the detection of glycopeptides from an human serum immunoglobulin G (IgG) tryptic digest in quantities as low as a 1:1250 molar ratio of IgG tryptic digest to bovine serum albumin tryptic digest. The novel nanocomposites were further used for the analysis of complex samples, and 1920 glycopeptide backbones from 775 glycoproteins were identified in three replicate analyses of 50 μg of proteins extracted from HeLa cell exosomes. The resulting highly informative mass spectra indicated that this multifunctional nanomaterial-based enrichment method could be used as a promising tool for the in-depth and comprehensive characterization of glycoproteomes in MS-based glycoproteomics.
基于质谱(MS)的糖蛋白质组学研究需要高效的样品制备,以消除非糖肽的干扰并提高糖肽检测效率。在这项工作中,制备了一种新型的 MoS/Au-NP(金纳米颗粒)-L-半胱氨酸纳米复合材料用于糖肽富集。二维(2D)结构的 MoS 纳米片作为基质,可以为固定具有低空间位阻的亲水性基团(如 L-半胱氨酸)提供较大的表面积,并且与糖肽之间的相互作用。结果,新型纳米材料具有出色的捕获糖肽的能力。与商业两性离子亲水相互作用色谱(ZIC-HILIC)材料相比,新型纳米材料表现出优异的富集性能,具有超高的选择性和灵敏度(约 10 fmol)、高结合能力(120 mg g)、高富集回收率(超过 93%)、满足批间重现性和良好的通用性,可用于糖肽富集。此外,通过检测人血清免疫球蛋白 G(IgG)胰蛋白酶消化物中的糖肽,证实了其对糖肽富集的出色特异性和效率,IgG 胰蛋白酶消化物与牛血清白蛋白胰蛋白酶消化物的摩尔比低至 1:1250。新型纳米复合材料还进一步用于复杂样品的分析,从 HeLa 细胞外泌体中提取的 50 μg 蛋白质的三次重复分析中鉴定出 775 种糖蛋白中的 1920 个糖肽主干。所得的信息量丰富的质谱表明,这种基于多功能纳米材料的富集方法可作为 MS 基于糖蛋白质组学中糖蛋白质组深入全面表征的有前途的工具。