Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark.
Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Campusvej 55, 5230 Odense M, Denmark.
J Am Chem Soc. 2023 Nov 8;145(44):23925-23938. doi: 10.1021/jacs.3c04068. Epub 2023 Oct 26.
Protein glycosylation is a common post-translational modification on extracellular proteins. The conformational dynamics of several glycoproteins have been characterized by hydrogen/deuterium exchange mass spectrometry (HDX-MS). However, it is, in most cases, not possible to extract information about glycan conformation and dynamics due to the general difficulty of separating the deuterium content of the glycan from that of the peptide (in particular, for O-linked glycans). Here, we investigate whether the fragmentation of protonated glycopeptides by collision-induced dissociation (CID) can be used to determine the solution-specific deuterium content of the glycan. Central to this concept is that glycopeptides can undergo a facile loss of glycans upon CID, thereby allowing for the determination of their masses. However, an essential prerequisite is that hydrogen and deuterium (H/D) scrambling can be kept in check. Therefore, we have measured the degree of scrambling upon glycosidic bond cleavage in glycopeptides that differ in the conformational flexibility of their backbone and glycosylation pattern. Our results show that complete scrambling precedes the glycosidic bond cleavage in normal glycopeptides derived from a glycoprotein; i.e., all labile hydrogens have undergone positional randomization prior to loss of the glycan. In contrast, the glycosidic bond cleavage occurs without any scrambling in the glycopeptide antibiotic vancomycin, reflecting that the glycan cannot interact with the peptide moiety due to a conformationally restricted backbone as revealed by molecular dynamics simulations. Scrambling is also inhibited, albeit to a lesser degree, in the conformationally restricted glycopeptides ristocetin and its pseudoaglycone, demonstrating that scrambling depends on an intricate interplay between the flexibility and proximity of the glycan and the peptide backbone.
蛋白质糖基化是细胞外蛋白常见的翻译后修饰。通过氢/氘交换质谱(HDX-MS)已经对几种糖蛋白的构象动力学进行了研究。然而,由于一般难以将聚糖的氘含量与肽的氘含量(特别是对于 O-连接的聚糖)分离,在大多数情况下,无法提取关于聚糖构象和动力学的信息。在这里,我们研究了通过碰撞诱导解离(CID)使质子化糖肽断裂是否可用于确定糖基的溶液特异性氘含量。这一概念的核心是糖肽可以在 CID 时轻易地失去聚糖,从而可以确定它们的质量。然而,一个基本的前提是氢和氘(H/D)交换可以得到控制。因此,我们已经测量了糖肽中糖苷键断裂时的交换程度,这些糖肽在其主链和糖基化模式的构象灵活性方面存在差异。我们的结果表明,在正常糖肽(源自糖蛋白)中,糖苷键断裂之前完全发生了交换,即所有不稳定的氢在失去聚糖之前已经经历了位置随机化。相比之下,在糖肽抗生素万古霉素中,糖苷键断裂没有任何交换,这反映出由于主链构象受限,聚糖无法与肽部分相互作用,如分子动力学模拟所揭示的。尽管程度较小,但在构象受限的糖肽 ristoctin 和其伪糖苷中,交换也受到抑制,这表明交换取决于聚糖和肽主链的灵活性和接近程度之间的复杂相互作用。