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寡孢节丛孢菌凝集素 AofleA 的异源表达及其分子结合特性研究。

Heterologous expression and molecular binding properties of AofleA, a fucose-specific lectin from nematophagous fungus Arthrobotrys oligospora.

机构信息

School of Life Sciences, Anhui University, Hefei 230601, Anhui, China; Key Laboratory of Human Microenvironment and Precision Medicine of Anhui Higher Education Institutes, Anhui University, Hefei 230601, Anhui, China; Anhui Key Laboratory of Modern Biomanufacturing, Hefei 230601, Anhui, China.

School of Life Sciences, Anhui University, Hefei 230601, Anhui, China; Key Laboratory of Human Microenvironment and Precision Medicine of Anhui Higher Education Institutes, Anhui University, Hefei 230601, Anhui, China.

出版信息

Int J Biol Macromol. 2020 Apr 15;149:1213-1221. doi: 10.1016/j.ijbiomac.2020.02.039. Epub 2020 Feb 6.

Abstract

Lectins are the primary recognition macromolecules for various types of fucosylation, a common eukaryotic post-translational modification. In this study, we report the heterologous expression and molecular binding properties of a fucose-specific lectin, AofleA, isolated from Arthrobotrys oligospora. This is the first reported fucose-specific lectin found in nematophagous fungi. The recombinant AofleA (r-AofleA) was expressed in Escherichia coli with high efficiency, yielding at least 500 mg of soluble and functional r-AofleA per liter of broth. Using hemagglutination inhibition assay and glycan microarray analysis, r-AofleA was found to be broadly specific for fucosylated glycans or oligosaccharides including Fucα(1-2), Fucα(1-3), Fucα(1-4) and Fucα(1-6) linkages, similar to Aleuria aurantia lectin (AAL). Frontal affinity chromatography showed that r-AofleA has high affinity towards PA-L-fucose with an average K value of 15 nM. These findings provide a basis for improved understanding of the structure and functions of AofleA during recognition and capture of prey nematodes by nematophagous fungus A. oligospora.

摘要

凝集素是各种类型岩藻糖基化的主要识别大分子,岩藻糖基化是一种常见的真核翻译后修饰。在本研究中,我们报告了一种从寡孢节丛孢菌中分离出的特异性识别岩藻糖的凝集素 AofleA 的异源表达及其分子结合特性。这是首次报道在食线虫真菌中发现的特异性识别岩藻糖的凝集素。重组 AofleA(r-AofleA)在大肠杆菌中高效表达,每升发酵液至少可产生 500 毫克可溶性和功能性的 r-AofleA。通过血凝抑制试验和糖芯片分析,发现 r-AofleA 广泛特异性识别岩藻糖基化聚糖或寡糖,包括 Fucα(1-2)、Fucα(1-3)、Fucα(1-4)和 Fucα(1-6)键,类似于金顶侧耳凝集素(AAL)。前沿亲和层析表明,r-AofleA 对 PA-L-岩藻糖具有高亲和力,平均 K 值为 15 nM。这些发现为深入了解食线虫真菌寡孢节丛孢菌在识别和捕获猎物线虫过程中 AofleA 的结构和功能提供了基础。

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