Ramadan Sherif, Su Guowei, Baryal Kedar, Hsieh-Wilson Linda C, Liu Jian, Huang Xuefei
Department of Chemistry, Michigan State University, 578 S. Shaw Lane, East Lansing, Michigan 48824, USA.
Chemistry Department, Faculty of Science, Benha University, Benha, Qaliobiya 13518, Egypt.
Org Chem Front. 2022 Jun 7;9(11):2910-2920. doi: 10.1039/d2qo00439a. Epub 2022 Apr 19.
Heparan sulfate (HS) regulates a wide range of biological events, including blood coagulation, cancer development, cell differentiation, and viral infections. It is generally recognized that structures of HS can critically impact its biological functions. However, with complex structures of naturally existing HS, systematic investigations into the structure-activity relationship (SAR) of HS and efforts to unlock their "sulfation code" have been largely limited due to the challenges in preparing diverse HS oligosaccharide sequences. Herein, we report an automated machine-aided solid-phase strategy that significantly expedited the assembly of HS disaccharides. The key strategically protected advanced disaccharide intermediates were immobilized onto Synphase lanterns. Divergent deprotections and sulfations of the disaccharides were achieved on the lanterns in high yields. In addition, the full synthetic process was automated, enabling the reproducible production of HS disaccharides. A library of 16 HS disaccharides with diverse sulfation patterns was prepared via this method. Compared to the traditional HS synthesis, this new strategy led to a reduction of 50% of the number of synthetic steps and over 80% of the number of column purification steps needed from the disaccharide intermediates, significantly improving the overall synthetic efficiency. The potential utility of the method was highlighted in a microarray study using the synthetic HS disaccharide library with fibroblast growth factor-2 (FGF-2), which yielded insights into the SAR of HS/FGF-2 interactions.
硫酸乙酰肝素(HS)调节广泛的生物事件,包括血液凝固、癌症发展、细胞分化和病毒感染。人们普遍认识到,HS的结构会对其生物学功能产生关键影响。然而,由于天然存在的HS结构复杂,制备多样的HS寡糖序列面临挑战,因此对HS结构-活性关系(SAR)的系统研究以及破解其“硫酸化密码”的努力在很大程度上受到限制。在此,我们报告了一种自动化的机器辅助固相策略,该策略显著加快了HS二糖的组装。关键的经过策略性保护的高级二糖中间体被固定在Synphase灯笼上。二糖的不同去保护和硫酸化反应在灯笼上以高产率实现。此外,整个合成过程实现了自动化,能够可重复地生产HS二糖。通过该方法制备了一个包含16种具有不同硫酸化模式的HS二糖文库。与传统的HS合成方法相比,这种新策略使合成步骤数量减少了50%,从二糖中间体所需的柱纯化步骤数量减少了80%以上,显著提高了整体合成效率。在使用合成HS二糖文库与成纤维细胞生长因子-2(FGF-2)进行的微阵列研究中突出了该方法的潜在实用性,该研究深入了解了HS/FGF-2相互作用的SAR。