Beccati Daniela, Lech Miroslaw, Ozug Jennifer, Gunay Nur Sibel, Wang Jing, Sun Elaine Y, Pradines Joël R, Farutin Victor, Shriver Zachary, Kaundinya Ganesh V, Capila Ishan
Momenta Pharmaceuticals Inc., 675 West Kendall Street, Cambridge, MA, 02142, USA.
Glycoconj J. 2017 Feb;34(1):107-117. doi: 10.1007/s10719-016-9734-7. Epub 2016 Oct 22.
Heparan sulfate (HS), a glycosaminoglycan present on the surface of cells, has been postulated to have important roles in driving both normal and pathological physiologies. The chemical structure and sulfation pattern (domain structure) of HS is believed to determine its biological function, to vary across tissue types, and to be modified in the context of disease. Characterization of HS requires isolation and purification of cell surface HS as a complex mixture. This process may introduce additional chemical modification of the native residues. In this study, we describe an approach towards thorough characterization of bovine kidney heparan sulfate (BKHS) that utilizes a variety of orthogonal analytical techniques (e.g. NMR, IP-RPHPLC, LC-MS). These techniques are applied to characterize this mixture at various levels including composition, fragment level, and overall chain properties. The combination of these techniques in many instances provides orthogonal views into the fine structure of HS, and in other instances provides overlapping / confirmatory information from different perspectives. Specifically, this approach enables quantitative determination of natural and modified saccharide residues in the HS chains, and identifies unusual structures. Analysis of partially digested HS chains allows for a better understanding of the domain structures within this mixture, and yields specific insights into the non-reducing end and reducing end structures of the chains. This approach outlines a useful framework that can be applied to elucidate HS structure and thereby provides means to advance understanding of its biological role and potential involvement in disease progression. In addition, the techniques described here can be applied to characterization of heparin from different sources.
硫酸乙酰肝素(HS)是一种存在于细胞表面的糖胺聚糖,据推测在驱动正常和病理生理过程中发挥着重要作用。HS的化学结构和硫酸化模式(结构域结构)被认为决定了其生物学功能,在不同组织类型中有所不同,并在疾病背景下发生改变。对HS的表征需要将细胞表面HS作为一种复杂混合物进行分离和纯化。这个过程可能会对天然残基引入额外的化学修饰。在本研究中,我们描述了一种对牛肾硫酸乙酰肝素(BKHS)进行全面表征的方法,该方法利用了多种正交分析技术(如核磁共振、离子对反相高效液相色谱、液相色谱 - 质谱)。这些技术被应用于在不同层面表征这种混合物,包括组成、片段层面和整体链性质。这些技术的组合在许多情况下能从正交视角深入了解HS的精细结构,在其他情况下能从不同角度提供重叠/确认信息。具体而言,这种方法能够定量测定HS链中天然和修饰的糖残基,并识别出异常结构。对部分消化的HS链进行分析有助于更好地理解该混合物中的结构域结构,并对链的非还原端和还原端结构产生具体见解。这种方法勾勒出了一个有用的框架,可用于阐明HS结构,从而为深入理解其生物学作用以及在疾病进展中的潜在参与提供手段。此外,这里描述的技术可应用于不同来源肝素的表征。