Kadonaga Yuichiro, Wang Ning, Shimoyama Atsushi, Fujimoto Yukari, Fukase Koichi
Division of Science, Institute for Radiation Sciences, The University of Osaka, 1-1 Machikaneyama, Toyonaka 560-0043, Osaka, Japan.
State Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, University of Chinese Academy of Sciences, 1 North 2nd Street, Zhongguancun, Haidian District, Beijing 100190, China.
Molecules. 2025 Jun 28;30(13):2787. doi: 10.3390/molecules30132787.
Peptidoglycan (PGN) is a component of bacterial cell walls; its fragments are recognized by the cytoplasmic receptors Nod1 and Nod2, thereby promoting the production of inflammatory cytokines and antibodies. To further elucidate these biological defense mechanisms, a large and stable supply of the PGN fragments via chemical synthesis is essential. However, the synthesis and purification of long PGN fragments are quite challenging due to their low solubility. In this study, we efficiently synthesized PGN fragments via solid-phase oligosaccharide synthesis (SPOS). Using the JandaJel™ Wang resin (JJ-Wang), an octasaccharide glycan chain of PGN was constructed by repeating glycosylation reactions to elongate β-1,4-linked disaccharide units composed of MurNAc and GlcNAc. To enhance reactivity, glycosylation was performed in a mixed solvent comprising CFOEt/CHCl/THF with the intention of promoting substrate concentration onto the solid support through the fluorophobic effect, affording the PGN octasaccharide in a 19% overall yield (10 steps). Subsequently, after deprotection of the -Fmoc, -Troc, and ethyl ester groups, - and -acetylation proceeded smoothly, owing to the high swelling property of JJ-Wang. Peptide condensation with L-Ala-D-isoGln(OBn) and carboxylic acids was also achieved. Finally, cleavage of the PGN fragment from the resin with TFA afforded the desired octasaccharide with dipeptides in a 2.3% overall yield (15 steps).
肽聚糖(PGN)是细菌细胞壁的一个组成部分;其片段可被细胞质受体Nod1和Nod2识别,从而促进炎性细胞因子和抗体的产生。为了进一步阐明这些生物防御机制,通过化学合成大量稳定供应PGN片段至关重要。然而,由于长PGN片段的低溶解性,其合成和纯化颇具挑战性。在本研究中,我们通过固相寡糖合成(SPOS)高效合成了PGN片段。使用JandaJel™ Wang树脂(JJ-Wang),通过重复糖基化反应构建了PGN的八糖聚糖链,以延长由MurNAc和GlcNAc组成的β-1,4-连接的二糖单元。为了提高反应活性,糖基化在包含CFOEt/CHCl/THF的混合溶剂中进行,目的是通过疏氟效应促进底物在固相载体上的浓度,以19%的总收率(10步)得到PGN八糖。随后,在-Fmoc、-Troc和乙酯基团脱保护后,由于JJ-Wang的高溶胀性,-和-乙酰化反应顺利进行。还实现了与L-Ala-D-isoGln(OBn)和羧酸的肽缩合。最后,用TFA从树脂上裂解PGN片段,以2.3%的总收率(15步)得到所需的带有二肽的八糖。