کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3425096 | 1227269 | 2010 | 11 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Gp15 and gp16 cooperate in translocating bacteriophage T7 DNA into the infected cell Gp15 and gp16 cooperate in translocating bacteriophage T7 DNA into the infected cell](/preview/png/3425096.png)
Loss of up to four amino acids from the C terminus of the 1318 residue bacteriophage T7 gp16 allows plaque formation at normal efficiencies. Loss of five residues results in non-infective virions, and loss of twelve prevents assembly of stable particles. However, replacing the C-terminal seven with nineteen non-native residues allows assembly of non-infective virions. The latter adsorb and eject internal core proteins into the cell envelope but no phage DNA enters the cytoplasm. Extragenic suppressors of the defective gene 16 lie in gene 15; the mutant gp15 proteins not only re-establish infectivity, they fully restore the kinetics of genome internalization to those exhibited by wild-type phage. After ejection from the infecting particle, gp15 and gp16 thus function together in ratcheting the leading end of the T7 genome into the cytoplasm of the infected cell.
Journal: Virology - Volume 398, Issue 2, 15 March 2010, Pages 176–186