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首页> 外文期刊>Journal of proteome research >Identification of Glycoproteins Carrying a Target Glycan-Motif by Liquid Chromatography/Multiple-Stage Mass Spectrometry: Identification of Lewis x-Conjugated Glycoproteins in Mouse Kidney
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Identification of Glycoproteins Carrying a Target Glycan-Motif by Liquid Chromatography/Multiple-Stage Mass Spectrometry: Identification of Lewis x-Conjugated Glycoproteins in Mouse Kidney

机译:液相色谱/多级质谱法鉴定携带目标糖基的糖蛋白:小鼠肾脏中Lewis x缀合糖蛋白的鉴定

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Certain glycan motifs in glycoproteins are involved in several biological events and diseases. To understand the roles of these motifs, a method is needed to identify the glycoproteins that carry them. We previously demonstrated that liquid chromatography-multiple-stage mass spectrometry (LC-MSn) allowed for differentiation of oligosaccharides attached to Lewis-motifs, such as Lewis x (Le(x), Gal beta 1-4(Fuc alpha 1-3)GlcNAc) from other glycans. We successfully discriminated Le(x)-conjugated oligosaccharides from other N-linked oligosaccharides derived from mouse kidney proteins by using Lewis-motif-distinctive ions, a deoxyhexose (dHex) + hexose (Hex) + N-acetylhexsosamine (HexNAc) fragment (m/z 512), and a Hex + HexNAc fragment (m/z 366). In the present study, we demonstrated that this method could be used to identify the Le(x)-conjugated glycoproteins. All proteins in the mouse kidney were digested into peptides, and the fucosylated glycopeptides were enriched by lectin-affinity chromatography. The resulting fucosylated glycopeptides were subjected to two different runs of LC-MSn using a Fourier-transform ion cyclotron resonance mass spectrometer (FTICR-MS) and an ion trap-type mass spectrometer. After the first run, we picked out product ion spectra of the expected Le(x)-conjugated glycopeptides based on the presence of Lewis-motif-distinctive ions and assigned a peptide + HexNAc or peptide + (dHex)HexNAc fragment in each spectrum. Then the fucosylated glycopeptides were subjected to a second run in which the peptide-related fragments were set as precursor ions. We successfully identified gamma-glutamyl transpeptidase 1 (gamma-GTP1), low-density lipoprotein receptor-related protein 2 (LRP2), and a cubilin precursor as Le(x)-conjugated glycoproteins by sequencing of 2-5 glycopeptides. In addition, it was deduced that cadherin 16, dipeptidase I, H-2 class I histocompatibility antigen, K-K alpha precursor (H2-K(k)), and alanyl (membrane) aminopeptidase could be Le(x)-conjugated glycoproteins from the good agreement between the experimental and theoretical masses and fragment patterns. The results indicated that our method could be applicable for the identification and screening of glycoproteins carrying target glycan-motifs, such as Lewis epitopes.
机译:糖蛋白中的某些聚糖基序与几种生物学事件和疾病有关。为了理解这些基序的作用,需要一种方法来鉴定携带它们的糖蛋白。我们以前证明了液相色谱多级质谱(LC-MSn)允许区分连接到Lewis-基序的寡糖,如Lewis x(Le(x),Gal beta 1-4(Fuc alpha 1-3) GlcNAc)来自其他聚糖。我们通过使用路易斯基序区分离子,脱氧己糖(dHex)+己糖(Hex)+ N-乙酰基己糖胺(HexNAc)片段(m / z 512)和一个Hex + HexNAc片段(m / z 366)。在本研究中,我们证明了该方法可用于鉴定Le(x)缀合的糖蛋白。将小鼠肾脏中的所有蛋白质消化成肽,并通过凝集素亲和层析富集岩藻糖基化的糖肽。使用傅立叶变换离子回旋共振质谱仪(FTICR-MS)和离子阱型质谱仪对所得的岩藻糖基化糖肽进行两次不同的LC-MSn分析。第一次运行后,我们根据路易斯-基序区分性离子的存在选择了预期的Le(x)-缀合的糖肽的产物离子光谱,并在每个光谱中分配了一个肽+ HexNAc或肽+(dHex)HexNAc片段。然后,将岩藻糖基化的糖肽进行第二轮,其中将肽相关的片段设置为前体离子。我们通过测序2-5个糖肽成功地确定了γ-谷氨酰转肽酶1(gamma-GTP1),低密度脂蛋白受体相关蛋白2(LRP2)和cubilin前体为Le(x)缀合的糖蛋白。此外,据推测,钙粘蛋白16,二肽酶I,H-2 I类组织相容性抗原,KKα前体(H2-K(k))和丙氨酰(膜)氨基肽酶可能是Le(x)结合的糖蛋白实验和理论质量与碎片模式之间的良好一致性。结果表明,我们的方法可用于鉴定和筛选带有目标聚糖基序的糖蛋白,如路易斯表位。

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