Pseudomonas Aeruginosa bacteriophage SN: 3D-reconstruction of the capsid and identification of surface proteins by electron microscopy

被引:0
|
作者
Filchikov, M. V. [1 ]
Osmakov, D. I. [1 ]
Logovskaya, L. V. [1 ]
Sykilinda, N. N. [1 ]
Kadykov, V. A. [1 ]
Kurochkina, L. P. [1 ]
Mesyanzhinov, V. V. [1 ]
Bernal, R. A. [2 ]
Miroshnikov, K. A. [1 ]
机构
[1] Russian Acad Sci, MM Shemyakin YuA Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
[2] Univ Texas El Paso, Dept Chem, El Paso, TX 79968 USA
基金
俄罗斯基础研究基金会;
关键词
Pseudomonas aeruginosa; bacteriophage SN; proteomics; structural proteins; cryo-electron microscopy; 3D-reconstruction; immuno-electron microscopy; ANGSTROM RESOLUTION; CRYO-EM; PHI-KZ; TAIL; SHEATH; MECHANISM; EVOLUTION; VIRUSES; COMPLEX; SYSTEM;
D O I
10.1134/S1068162009060089
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The virulent Pseudomonas aeruginosa bacteriophage SN belongs to the PB1-like species of the Myoviridae family. The comparatively small (66,391 bp) DNA genome of this phage encodes 89 predicted open reading frames and the proteome involves more than 20 structural proteins. A 3D model of the phage capsid to approximately 18 resolution reveals certain peculiarities of capsomer structure typical of only this bacteriophage species. In the present work recombinant structural proteins SN gp22 and gp29 were expressed and purified; and specific polyclonal antibodies were obtained. Immuno-electron microscopy of purified phage SN using secondary gold-conjugated antibodies has revealed that gp29 forms a phage sheath, and gp22 decorates the capsid. Precise identification of multicopy major capsid proteins is essential for subsequent construction of gene-engineered phages bearing non-native peptides on their surfaces (phage display).
引用
收藏
页码:728 / 733
页数:6
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