Institute of Plant Genetics, Italian National Council of Research (CNR), Perugia, Italy.
Plant Biotechnol J. 2011 Dec;9(9):1061-73. doi: 10.1111/j.1467-7652.2011.00630.x. Epub 2011 Jun 7.
Deficiency in human lysosomal α-mannosidase (MAN2B1) results in α-mannosidosis, a lysosomal storage disorder; patients present a wide range of neurological, immunological, and skeletal symptoms caused by a multisystemic accumulation of mannose-containing oligosaccharides. Here, we describe the expression of recombinant MAN2B1 both transiently in Nicotiana benthamiana leaves and in the leaves and seeds of stably transformed N. tabacum plants. After purification from tobacco leaves, the recombinant enzyme was found to be N-glycosylated and localized in vacuolar compartments. In the fresh leaves of tobacco transformants, MAN2B1 was measured at 10,200 units/kg, and the purified enzyme from these leaves had a specific activity of 32-45 U/mg. Furthermore, tobacco-produced MAN2B1 was biochemically similar to the enzyme purified from human tissues, and it was internalized and processed by α-mannosidosis fibroblast cells. These results strongly indicate that plants can be considered a promising expression system for the production of recombinant MAN2B1 for use in enzyme replacement therapy.
人类溶酶体α-甘露糖苷酶(MAN2B1)缺乏会导致α-甘露糖苷症,这是一种溶酶体贮积病;患者表现出广泛的神经系统、免疫学和骨骼症状,这是由于甘露糖结合寡糖在多系统中的积累引起的。在这里,我们描述了重组 MAN2B1 在烟草瞬时表达和稳定转化的烟草叶片和种子中的表达。从烟草叶片中纯化后,发现重组酶发生了 N 糖基化,并定位于液泡区室中。在烟草转化体的新鲜叶片中,MAN2B1 的含量为 10200 单位/千克,从这些叶片中纯化的酶的比活度为 32-45 U/mg。此外,烟草产生的 MAN2B1 在生化上与从人组织中纯化的酶相似,并且被α-甘露糖苷症成纤维细胞内化和加工。这些结果强烈表明,植物可以被视为生产用于酶替代治疗的重组 MAN2B1 的有前途的表达系统。