Department of Medical Biochemistry, University of Gothenburg, SE 405 30 Gothenburg, Sweden; email:
Annu Rev Biochem. 2020 Jun 20;89:769-793. doi: 10.1146/annurev-biochem-011520-105053. Epub 2020 Apr 3.
Generating the barriers that protect our inner surfaces from bacteria and other challenges requires large glycoproteins called mucins. These come in two types, gel-forming and transmembrane, all characterized by large, highly -glycosylated mucin domains that are diversely decorated by Golgi glycosyltransferases to become extended rodlike structures. The general functions of mucins on internal epithelial surfaces are to wash away microorganisms and, even more importantly, to build protective barriers. The latter function is most evident in the large intestine, where the inner mucus layer separates the numerous commensal bacteria from the epithelial cells. The host's conversion of MUC2 to the outer mucus layer allows bacteria to degrade the mucin glycans and recover the energy content that is then shared with the host. The molecular nature of the mucins is complex, and how they construct the extracellular complex glycocalyx and mucus is poorly understood and a future biochemical challenge.
生成保护我们的内表面免受细菌和其他挑战的屏障需要称为粘蛋白的大型糖蛋白。这些分为两种类型,即形成凝胶的和跨膜的,它们都具有大的、高度糖基化的粘蛋白结构域,这些结构域通过高尔基体糖基转移酶的多样化修饰,成为延伸的棒状结构。粘蛋白在内皮表面的一般功能是冲走微生物,更重要的是,构建保护屏障。后者的功能在大肠中最为明显,其中内层黏液层将大量共生细菌与上皮细胞分开。宿主将 MUC2 转化为外层黏液层,使细菌能够降解粘蛋白聚糖并回收能量,然后与宿主共享。粘蛋白的分子性质很复杂,它们如何构建细胞外复杂的糖萼和黏液还知之甚少,这是未来生化方面的挑战。