Taniguchi T, Guarente L, Roberts T M, Kimelman D, Douhan J, Ptashne M
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5230-3. doi: 10.1073/pnas.77.9.5230.
We applied the method of Guarente et al. [Guarente, L., Lauer, G., Roberts, T.M. & Ptashne, M. (1980) Cell 20, 543-553] to construct plasmids that direct expression in Escherichia coli of the human fibroblast interferon (F-IF) gene. Two plasmids were recovered. One directs efficient synthesis of a protein whose primary sequence is that of pre-F-IF and the other, that of mature F-IF. Extracts of bacteria synthesizing mature F-IF display antiviral activity characteristic of human F-IF. This activity is lower than that expected from the differential rate of synthesis of the protein. We have detected no such activity in extracts of bacteria synthesizing pre-F-IF.
我们采用了瓜伦特等人[瓜伦特,L.,劳尔,G.,罗伯茨,T.M.和普塔什内,M.(1980年)《细胞》20卷,543 - 553页]的方法来构建可在大肠杆菌中指导人成纤维细胞干扰素(F - IF)基因表达的质粒。回收了两种质粒。一种可高效合成一种蛋白质,其一级序列为前F - IF的序列,另一种为成熟F - IF的序列。合成成熟F - IF的细菌提取物表现出人类F - IF特有的抗病毒活性。该活性低于根据该蛋白质的差异合成速率所预期的活性。我们在合成前F - IF的细菌提取物中未检测到此类活性。