Structure of epsilon15 bacteriophage reveals genome organization and DNA packaging/injection apparatus

被引:246
作者
Jiang, W
Chang, J
Jakana, J
Weigele, P
King, J
Chiu, W [1 ]
机构
[1] Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA
[2] Baylor Coll Med, Grad Program Struct & Computat Biol & Mol Biophys, Houston, TX 77030 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1038/nature04487
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The critical viral components for packaging DNA, recognizing and binding to host cells, and injecting the condensed DNA into the host are organized at a single vertex of many icosahedral viruses. These component structures do not share icosahedral symmetry and cannot be resolved using a conventional icosahedral averaging method. Here we report the structure of the entire infectious Salmonella bacteriophage epsilon15 ( ref. 1) determined from single-particle cryo-electron microscopy, without icosahedral averaging. This structure displays not only the icosahedral shell of 60 hexamers and 11 pentamers, but also the non-icosahedral components at one pentameric vertex. The densities at this vertex can be identified as the 12-subunit portal complex sandwiched between an internal cylindrical core and an external tail hub connecting to six projecting trimeric tailspikes. The viral genome is packed as coaxial coils in at least three outer layers with similar to 90 terminal nucleotides extending through the protein core and the portal complex and poised for injection. The shell protein from icosahedral reconstruction at higher resolution exhibits a similar fold to that of other double-stranded DNA viruses including herpesvirus(2-6), suggesting a common ancestor among these diverse viruses. The image reconstruction approach should be applicable to studying other biological nanomachines with components of mixed symmetries.
引用
收藏
页码:612 / 616
页数:5
相关论文
共 28 条
[1]   Structure of the connector of bacteriophage T7 at 8 Å resolution:: Structural homologies of a basic component of a DNA translocating machinery [J].
Agirrezabala, X ;
Martín-Benito, J ;
Valle, M ;
González, JM ;
Valencia, A ;
Valpuesta, JM ;
Carrascosa, JL .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 347 (05) :895-902
[2]   Investigation of viral DNA packaging using molecular mechanics models [J].
Arsuaga, J ;
Tan, RKZ ;
Vazquez, M ;
Sumners, DW ;
Harvey, SC .
BIOPHYSICAL CHEMISTRY, 2002, 101 :475-484
[3]   Common ancestry of herpesviruses and tailed DNA bacteriophages [J].
Baker, ML ;
Jiang, W ;
Rixon, FJ ;
Chiu, W .
JOURNAL OF VIROLOGY, 2005, 79 (23) :14967-14970
[4]  
BAZINET C, 1985, ANNU REV MICROBIOL, V39, P109
[5]   A 9 Å single particle reconstruction from CCD captured images on a 200 kV electron cryomicroscope [J].
Booth, CR ;
Jiang, W ;
Baker, ML ;
Zhou, ZH ;
Ludtke, SJ ;
Chiu, W .
JOURNAL OF STRUCTURAL BIOLOGY, 2004, 147 (02) :116-127
[6]  
BREITBART M, 2005, PHAGES THEIR ROLE BA, P66
[7]   BACTERIOPHAGE-T3 GENE-8 PRODUCT OLIGOMER STRUCTURE [J].
CARAZO, JM ;
FUJISAWA, H ;
NAKASU, S ;
CARRASCOSA, JL .
JOURNAL OF ULTRASTRUCTURE AND MOLECULAR STRUCTURE RESEARCH, 1986, 94 (02) :105-113
[8]   Encapsidated conformation of bacteriophage T7 DNA [J].
Cerritelli, ME ;
Cheng, NQ ;
Rosenberg, AH ;
McPherson, CE ;
Booy, FP ;
Steven, AC .
CELL, 1997, 91 (02) :271-280
[9]   A second symmetry mismatch at the portal vertex of bacteriophage T7: 8-fold symmetry in the procapsid core [J].
Cerritelli, ME ;
Trus, BL ;
Smith, CS ;
Cheng, NQ ;
Conway, JF ;
Steven, AC .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 327 (01) :1-6
[10]   CRYO-ELECTRON MICROSCOPY OF VITRIFIED SPECIMENS [J].
DUBOCHET, J ;
ADRIAN, M ;
CHANG, JJ ;
HOMO, JC ;
LEPAULT, J ;
MCDOWALL, AW ;
SCHULTZ, P .
QUARTERLY REVIEWS OF BIOPHYSICS, 1988, 21 (02) :129-228