TY - JOUR
T1 - Chlamydiaphage Chp2, a skeleton in the φX174 closet
T2 - Scaffolding protein and procapsid identification
AU - Clarke, Ian N.
AU - Cutcliffe, Leslie T.
AU - Everson, J. Sylvia
AU - Garner, Sarah A.
AU - Lambden, Paul R.
AU - Pead, Paddy J.
AU - Pickett, Mark A.
AU - Brentlinger, Karie L.
AU - Fane, Bentley A.
PY - 2004/11
Y1 - 2004/11
N2 - Chlamydiaphage Chp2 is a member of the family Microviridae, of which bacteriophage φX174 is the type species. Although grouped in the same family, the relationship between the Microviridae coliphages and the Chp2-like viruses, which infect obligate intracellular parasitic bacteria, is quite distant, with major differences in structural protein content and scaffolding protein dependence. To investigate the morphogenesis of Chp2, large particles were isolated from infected Chlamydophila abortus by equilibrium and rate zonal sedimentation. A monoclonal antibody that recognizes only assembled viral coat proteins was used in these detection assays. Thus, the detected particles represent virions and/or postcapsid formation assembly intermediates. Two distinct particle types were detected, differing in both protein and DNA content. Filled particles lacked VP3, the putative internal scaffolding protein, whereas empty particles contained this protein. These results indicate that VP3 is a scaffolding protein and that the isolated VP3-containing particles most likely represent Chp2 procapsids.
AB - Chlamydiaphage Chp2 is a member of the family Microviridae, of which bacteriophage φX174 is the type species. Although grouped in the same family, the relationship between the Microviridae coliphages and the Chp2-like viruses, which infect obligate intracellular parasitic bacteria, is quite distant, with major differences in structural protein content and scaffolding protein dependence. To investigate the morphogenesis of Chp2, large particles were isolated from infected Chlamydophila abortus by equilibrium and rate zonal sedimentation. A monoclonal antibody that recognizes only assembled viral coat proteins was used in these detection assays. Thus, the detected particles represent virions and/or postcapsid formation assembly intermediates. Two distinct particle types were detected, differing in both protein and DNA content. Filled particles lacked VP3, the putative internal scaffolding protein, whereas empty particles contained this protein. These results indicate that VP3 is a scaffolding protein and that the isolated VP3-containing particles most likely represent Chp2 procapsids.
UR - http://www.scopus.com/inward/record.url?scp=7744235345&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=7744235345&partnerID=8YFLogxK
U2 - 10.1128/JB.186.22.7571-7574.2004
DO - 10.1128/JB.186.22.7571-7574.2004
M3 - Article
C2 - 15516569
AN - SCOPUS:7744235345
SN - 0021-9193
VL - 186
SP - 7571
EP - 7574
JO - Journal of bacteriology
JF - Journal of bacteriology
IS - 22
ER -