Jiang Hui, Desaire Heather, Butnev Vladimir Y, Bousfield George R
Department of Chemistry, University of Kansas, Lawrence, Kansas 66045, USA.
J Am Soc Mass Spectrom. 2004 May;15(5):750-8. doi: 10.1016/j.jasms.2004.01.009.
This work compares several different methods of site-specific analysis of glycoproteins using electrospray mass spectrometry. The glycoprotein, oLHalpha (ovine luteinizing hormone, alpha-subunit) was chosen as an appropriate example protein for these studies because of its biological relevance and extreme microheterogeneity. More than 20 unique glycoforms were detected for this glycoprotein at the Asn(56) site of oLHalpha. The carbohydrates present at this site affect receptor binding affinity, so understanding the great variety in the composition of these carbohydrates is important in studying ligand binding interactions. MS data was acquired on a quadrupole ion trap, a triple quadrupole, and a quadrupole time of flight mass spectrometer, and carbohydrate composition at the Asn(56) site of oLHalpha was determined using these instruments. Additionally, neutral loss and precursor ion scanning modes were also used to identify the glycoforms present, and these techniques were compared to the standard MS data. Of the three instruments compared in the study, the qTOF mass spectrometer achieved the lowest sample consumption, but all three instruments were useful in profiling the glycopeptide composition.
这项工作使用电喷雾质谱法比较了几种不同的糖蛋白位点特异性分析方法。糖蛋白oLHα(绵羊促黄体激素α亚基)因其生物学相关性和极端微观异质性,被选为这些研究的合适示例蛋白。在oLHα的Asn(56)位点检测到该糖蛋白有20多种独特的糖型。该位点存在的碳水化合物会影响受体结合亲和力,因此了解这些碳水化合物组成的多样性对于研究配体结合相互作用很重要。在四极杆离子阱、三重四极杆和四极杆飞行时间质谱仪上采集了质谱数据,并使用这些仪器确定了oLHα的Asn(56)位点的碳水化合物组成。此外,还使用中性丢失和前体离子扫描模式来识别存在的糖型,并将这些技术与标准质谱数据进行了比较。在该研究中比较的三种仪器中,四极杆飞行时间质谱仪的样品消耗量最低,但所有三种仪器都有助于分析糖肽组成。