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利用瞬时表达系统在本氏烟草中克隆和表达人釉原蛋白的分析

Cloning and Expression Analysis of Human Amelogenin in Nicotiana benthamiana Plants by Means of a Transient Expression System.

作者信息

Pegoraro Mattia, Matić Slavica, Pergolizzi Barbara, Iannarelli Luca, Rossi Andrea M, Morra Marco, Noris Emanuela

机构信息

Institute for Sustainable Plant Protection, National Research Council of Italy (IPSP-CNR), Strada delle Cacce 73, 10135, Turin, Italy.

Dipartimento di Scienze Agrarie, Forestali e Alimentari, Entomologia, University of Torino, Grugliasco (TO), Italy.

出版信息

Mol Biotechnol. 2017 Oct;59(9-10):425-434. doi: 10.1007/s12033-017-0030-y.

Abstract

Enamel is the covering tissue of teeth, made of regularly arranged hydroxyapatite crystals deposited on an organic matrix composed of 90% amelogenin that is completely degraded at the end of the enamel formation process. Amelogenin has a biomineralizing activity, forming nanoparticles or nanoribbons that guide hydroxyapatite deposit, and regenerative functions in bone and vascular tissue and in wound healing. Biotechnological products containing amelogenin seem to facilitate these processes. Here, we describe the production of human amelogenin in plants by transient transformation of Nicotiana benthamiana with constructs carrying synthetic genes with optimized human or plant codons. Both genes yielded approximately 500 µg of total amelogenin per gram of fresh leaf tissue. Two purification procedures based on affinity chromatography or on intrinsic solubility properties of the protein were followed, yielding from 12 to 150 µg of amelogenin per gram of fresh leaf tissue, respectively, at different purity. The identity of the plant-made human amelogenin was confirmed by MALDI-TOF-MS analysis of peptides generated following chymotrypsin digestion. Using dynamic light scattering, we showed that plant extracts made in acetic acid containing human amelogenin have a bimodal distribution of agglomerates, with hydrodynamic diameters of 22.8 ± 3.8 and 389.5 ± 86.6 nm. To the best of our knowledge, this is the first report of expression of human amelogenin in plants, offering the possibility to use this plant-made protein for nanotechnological applications.

摘要

牙釉质是牙齿的覆盖组织,由规则排列的羟基磷灰石晶体沉积在有机基质上构成,该有机基质由90%的釉原蛋白组成,在牙釉质形成过程结束时会完全降解。釉原蛋白具有生物矿化活性,可形成引导羟基磷灰石沉积的纳米颗粒或纳米带,并且在骨组织、血管组织及伤口愈合中具有再生功能。含有釉原蛋白的生物技术产品似乎能促进这些过程。在此,我们描述了通过用携带经优化的人类或植物密码子的合成基因的构建体瞬时转化本氏烟草,在植物中生产人类釉原蛋白的方法。这两种基因每克新鲜叶片组织均产生约500微克的总釉原蛋白。随后采用了基于亲和色谱或基于蛋白质固有溶解性的两种纯化方法,分别从每克新鲜叶片组织中获得了12至150微克不同纯度的釉原蛋白。通过对胰凝乳蛋白酶消化后产生的肽段进行基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)分析,证实了植物制造的人类釉原蛋白的身份。使用动态光散射技术,我们表明在含有人釉原蛋白的醋酸中制备的植物提取物具有双峰聚集体分布,流体动力学直径分别为22.8±3.8纳米和389.5±86.6纳米。据我们所知,这是关于人类釉原蛋白在植物中表达的首次报道,为将这种植物制造的蛋白质用于纳米技术应用提供了可能性。

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