Department of Gastrointestinal Surgery, China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Beijing 100029, PR China.
Medical and Healthy Analysis Center, Beijing Key Laboratory of Tumor Systems Biology, Peking University, Xueyuan Road 38, Haidian District, Beijing 100191, PR China.
J Chromatogr A. 2020 Jan 11;1610:460546. doi: 10.1016/j.chroma.2019.460546. Epub 2019 Sep 16.
Selective enrichment of glycopeptides from complex sample with hydrophilic interaction liquid chromatography (HILIC) method, followed by cleavage of N-glycans by PNGase F to expose an easily detectable mark on the former glycosylation sites is used extensively as a sample preparation for comprehensive glycoproteome analysis. However, the coenrichment of hydrophilic nonglycosylated peptides and the released N-glycans seriously affect the identification of deglycopeptides with nano-LC-MS/MS. Here, we developed a new method for highly efficient and specific enrichment of human plasma N-glycopeptides using HILIC-PNGaseF-HILIC workflow (HPH). The first HILIC enriches the N-glycopeptides from the complex peptide mixtures. After the enriched N-glycopeptides are deglycosylated with PNGase F, the second HILIC captures the coenrichment of hydrophilic nonglycosylated peptides and the N-glycans, and then further enriches the deglycosylated peptides. The glycopeptide enrichment efficiency can be notably improved by employing HPH, evaluated by the highly recovery (more than 93.6%) and specific capturing glycopeptides from tryptic digest of IgG and BSA up to the molar ratios of 1:200. Meanwhile, we found that the alkylated proteins with IAA can affect the enrichment efficiency for N-glycopeptides with HILIC method. Moreover, after optimism the protein digestion, this novel HPH strategy allowed for the identified 722 N-glycopeptides within 202 unique glycoproteins from 1 µL human plasma digest using PNGase F in HO. Meanwhile, this new HPH strategy identified an average 501 N-glycopeptides within averagely 134 unique glycoproteins from 1 µL human plasma digest using PNGase F in HO. The enhanced glycopeptide detection was promoted by a substantial depletion of nonglycosylated peptides in the second HILIC. It was found that 52.2% more N-glycosylation peptides were identified by the HPH strategy compared with the using one HILIC enrichment alone.
采用亲水作用色谱(HILIC)法从复杂样品中选择性富集糖肽,然后用 PNGase F 切割 N-糖链,暴露出以前糖基化位点上易于检测的标记,这种方法被广泛用于全面糖蛋白质组分析的样品制备。然而,亲水性非糖肽和释放的 N-糖链的共富集严重影响了用纳升液相色谱-串联质谱(nano-LC-MS/MS)鉴定去糖肽。在这里,我们开发了一种使用 HILIC-PNGaseF-HILIC 工作流程(HPH)高效且特异性富集人血浆 N-糖肽的新方法。第一 HILIC 从复杂的肽混合物中富集 N-糖肽。在用 PNGase F 对富集的 N-糖肽进行去糖基化后,第二 HILIC 捕获亲水性非糖肽和 N-糖链的共富集物,然后进一步富集去糖基化的肽。通过采用 HPH,可以显著提高糖肽的富集效率,从 IgG 和 BSA 的胰蛋白酶消化物中以高达 1:200 的摩尔比高度回收(超过 93.6%)和特异性捕获糖肽来评估。同时,我们发现用 IAA 烷基化的蛋白质会影响用 HILIC 方法富集 N-糖肽的效率。此外,在优化蛋白消化后,这种新的 HPH 策略允许在 HO 中使用 PNGase F 从 1 µL 人血浆消化物中鉴定出 722 个 N-糖肽,在 202 个独特糖蛋白中鉴定出 722 个 N-糖肽。同时,这种新的 HPH 策略允许在 HO 中使用 PNGase F 从 1 µL 人血浆消化物中鉴定出 722 个 N-糖肽,在 202 个独特糖蛋白中鉴定出 722 个 N-糖肽。在第二 HILIC 中大量耗尽非糖肽,促进了糖肽的检测增强。结果发现,与单独使用一次 HILIC 富集相比,HPH 策略鉴定到的 N-糖肽多了 52.2%。