Lin Q, Chen Z C, Antoniw J F, White R F
Department of Plant Pathology, AFRC Institute of Arable Crops Research, Rothamsted Experimental Station, Harpenden, Herts, UK.
Plant Mol Biol. 1991 Oct;17(4):609-14. doi: 10.1007/BF00037047.
Phytolacca anti-viral protein (PAP) was purified from Phytolacca leaves and the N-terminal was sequenced. A cDNA library was made from mRNAs isolated from Phytolacca leaves and cDNA clones for PAP were identified using oligonucleotide probes derived from the N-terminal amino acid sequence. The PAP-cDNA clone was sequenced from both directions. The predicted amino acid sequence of PAP was compared with the amino acid sequences of other ribosome-inactivating proteins. The identities of these proteins to PAP ranged from 29 to 38%, and a region was found in each with a sequence similar to the PAP sequence (AIQMVSEAARFKYI). Southern blot analysis indicates that PAP is encoded by a multi-gene family.
从商陆叶中纯化出商陆抗病毒蛋白(PAP)并对其N端进行测序。用从商陆叶中分离的mRNA构建了一个cDNA文库,并使用从N端氨基酸序列推导而来的寡核苷酸探针鉴定出PAP的cDNA克隆。从两个方向对PAP-cDNA克隆进行测序。将预测的PAP氨基酸序列与其他核糖体失活蛋白的氨基酸序列进行比较。这些蛋白质与PAP的同源性在29%至38%之间,并且在每个蛋白质中都发现了一个与PAP序列(AIQMVSEAARFKYI)相似的区域。Southern印迹分析表明PAP由一个多基因家族编码。