van der Kaaij Alex, van Noort Kim, Nibbering Pieter, Wilbers Ruud H P, Schots Arjen
Laboratory of Nematology, Plant Sciences Group, Wageningen University and Research, Wageningen, Netherlands.
Front Plant Sci. 2022 Apr 29;13:882835. doi: 10.3389/fpls.2022.882835. eCollection 2022.
Glycoproteins are the dominant category among approved biopharmaceuticals, indicating their importance as therapeutic proteins. Glycoproteins are decorated with carbohydrate structures (or glycans) in a process called glycosylation. Glycosylation is a post-translational modification that is present in all kingdoms of life, albeit with differences in core modifications, terminal glycan structures, and incorporation of different sugar residues. Glycans play pivotal roles in many biological processes and can impact the efficacy of therapeutic glycoproteins. The majority of biopharmaceuticals are based on human glycoproteins, but non-human glycoproteins, originating from for instance parasitic worms (helminths), form an untapped pool of potential therapeutics for immune-related diseases and vaccine candidates. The production of sufficient quantities of correctly glycosylated putative therapeutic helminth proteins is often challenging and requires extensive engineering of the glycosylation pathway. Therefore, a flexible glycoprotein production system is required that allows straightforward introduction of heterologous glycosylation machinery composed of glycosyltransferases and glycosidases to obtain desired glycan structures. The glycome of plants creates an ideal starting point for - and -glyco-engineering of helminth glycans. Plants are also tolerant toward the introduction of heterologous glycosylation enzymes as well as the obtained glycans. Thus, a potent production platform emerges that enables the production of recombinant helminth proteins with unusual glycans. In this review, we discuss recent advances in plant glyco-engineering of potentially therapeutic helminth glycoproteins, challenges and their future prospects.
糖蛋白是已获批生物制药中的主要类别,这表明它们作为治疗性蛋白质的重要性。糖蛋白在一个称为糖基化的过程中被碳水化合物结构(或聚糖)修饰。糖基化是一种翻译后修饰,存在于所有生命王国中,尽管在核心修饰、末端聚糖结构以及不同糖残基的掺入方面存在差异。聚糖在许多生物过程中发挥着关键作用,并会影响治疗性糖蛋白的功效。大多数生物制药都基于人类糖蛋白,但源自例如寄生虫(蠕虫)的非人类糖蛋白,构成了免疫相关疾病潜在治疗药物和候选疫苗的未开发资源库。生产足够数量的正确糖基化的假定治疗性蠕虫蛋白往往具有挑战性,需要对糖基化途径进行广泛的工程改造。因此,需要一个灵活的糖蛋白生产系统,该系统允许直接引入由糖基转移酶和糖苷酶组成的异源糖基化机制,以获得所需的聚糖结构。植物的糖组为蠕虫聚糖的糖基工程创造了一个理想的起点。植物也能耐受异源糖基化酶以及所获得的聚糖的引入。因此,一个强大的生产平台应运而生,能够生产具有异常聚糖的重组蠕虫蛋白。在这篇综述中,我们讨论了植物对潜在治疗性蠕虫糖蛋白进行糖基工程的最新进展、挑战及其未来前景。