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首页> 外文期刊>Analytical chemistry >Ion Mobility-Mass Spectrometry of Complex Carbohydrates: Collision Cross Sections of Sodiated N-linked Glycans
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Ion Mobility-Mass Spectrometry of Complex Carbohydrates: Collision Cross Sections of Sodiated N-linked Glycans

机译:复杂碳水化合物的离子淌度-质谱:固结的N-连接聚糖的碰撞截面

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摘要

Currently, the vast majority of complex carbohydrates are characterized using mass spectrometry (MS)-based techniques. Measuring the molecular mass of a sugar, however, immediately poses a fundamental problem: entire classes of the constituting monosaccharide building blocks exhibit an identical atomic composition and, consequently, also an identical mass. Therefore, carbohydrate MS data can be highly ambiguous and often it is simply not possible to clearly assign a particular molecular structure. A promising approach to overcome the above-mentioned limitation is to implement an additional gas-phase separation dimension using ion mobility spectrometry (IMS), which is a method in which molecules of identical mass and structure but different structure can be separated according to their shape and collision cross section (CCS). With the emergence of commercially available hybrid ion mobility-mass spectrometry (IM-MS) instruments in 2006, IMS technology became readily available. Because of the nonhomogeneous, traveling wave (TW) field utilized in these instruments, however, CCS values currently cannot be determined directly from the drift times measured. Instead, an external calibration using compounds of known CCS and similar molecular identity is required. Here, we report a calibration protocol for TW IMS instruments using a series of sodiated N-glycans that were released from commercially available glycoproteins using an easy-to-follow protocol. The underlying CCS values were determined using a modified Synapt HDMS instrument with a linear drift tube, which was described in detail previously. Our data indicate that, under in-source fragmentation conditions, only a few glycans are required to obtain a TW IMS calibration of sufficient quality. In this context, however, the type of glycan was shown to be of tremendous importance. Furthermore, our data clearly demonstrate that carbohydrate isomers with identical mass but different conformation can be distinguished based on their CCS when all the associated errors are taken into account.
机译:当前,绝大多数复杂碳水化合物都使用基于质谱(MS)的技术进行表征。然而,测量糖的分子质量会立即引起一个基本问题:所有构成单糖的结构单元类别都具有相同的原子组成,因此也具有相同的质量。因此,碳水化合物MS数据可能非常含糊,通常根本不可能明确指定特定的分子结构。克服上述局限性的一种有前途的方法是使用离子迁移谱(IMS)来实现附加的气相分离尺寸,该方法是可以根据其形状将质量和结构相同但结构不同的分子分离的方法和碰撞截面(CCS)。随着2006年商用混合离子迁移率质谱(IM-MS)仪器的出现,IMS技术变得很容易获得。但是,由于这些仪器使用了非均匀的行波(TW)场,因此,当前无法直接从测量的漂移时间确定CCS值。相反,需要使用已知CCS和相似分子同一性的化合物进行外部校准。在这里,我们报告了一系列易于使用的N-聚糖从商用糖蛋白中释放出来的一系列标准化的TW IMS仪器的校准方案。基本CCS值是使用改良的带有线性漂移管的Synapt HDMS仪器确定的,之前已对此进行了详细介绍。我们的数据表明,在源内裂解条件下,仅需少数聚糖即可获得足够质量的TW IMS校准。然而,在这种情况下,显示出聚糖的类型非常重要。此外,我们的数据清楚地表明,当考虑所有相关错误时,可以基于其CCS区分质量相同但构象不同的碳水化合物异构体。

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