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槲寄生核糖体失活蛋白MLIII催化亚基的克隆与表达

Cloning and expression of catalytic subunit of MLIII, the ribosome-inactivating protein from Viscum album.

作者信息

Tonevitsky A G, Agapov I I, Pevzner I B, Malyuchenko N V, Moisenovich M M, Pfueller U, Kirpichnikov M P

机构信息

Faculty of Biology, Lomonosov Moscow State University, Moscow 119899, Russia.

出版信息

Biochemistry (Mosc). 2004 Jun;69(6):642-50. doi: 10.1023/b:biry.0000033737.79960.a7.

Abstract

We have cloned the gene encoding a precursor of mistletoe (Viscum album) toxin MLIII. Analyses of nucleotide and deduced amino acid sequences of this gene revealed significant differences between MLI and MLIII preprotoxin genes. Immunochemical properties of recombinant A-subunit expressed in Escherichia coli and renatured were investigated using a panel of monoclonal antibodies raised against three mistletoe toxins (MLI, MLII, and MLIII). Ribosome-inactivating activity of recombinant MLIII A-subunit was detected in cell-free lysate of rabbit reticulocytes.

摘要

我们已经克隆了编码槲寄生(白果槲寄生)毒素MLIII前体的基因。对该基因的核苷酸和推导的氨基酸序列分析显示,MLI和MLIII前原毒素基因之间存在显著差异。使用针对三种槲寄生毒素(MLI、MLII和MLIII)产生的一组单克隆抗体,研究了在大肠杆菌中表达并复性的重组A亚基的免疫化学特性。在兔网织红细胞的无细胞裂解物中检测到了重组MLIII A亚基的核糖体失活活性。

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