scholarly journals Visualization of Single Molecules Building a Viral Capsid Protein Lattice through Stochastic Pathways

ACS Nano ◽  
2020 ◽  
Vol 14 (7) ◽  
pp. 8724-8734
Author(s):  
Alejandro Valbuena ◽  
Sourav Maity ◽  
Mauricio G. Mateu ◽  
Wouter H. Roos
2011 ◽  
Vol 86 (6) ◽  
pp. 3318-3326 ◽  
Author(s):  
R. D. Cadena-Nava ◽  
M. Comas-Garcia ◽  
R. F. Garmann ◽  
A. L. N. Rao ◽  
C. M. Knobler ◽  
...  

2006 ◽  
Vol 94 (6) ◽  
pp. 1129-1137 ◽  
Author(s):  
Maggie Y.T. Lee ◽  
Yuanxiang Zhou ◽  
Raymond W.M. Lung ◽  
Mee-Len Chye ◽  
Wing-Kin Yip ◽  
...  

1973 ◽  
Vol 19 (2) ◽  
pp. 299-301 ◽  
Author(s):  
Lorne A. Babiuk ◽  
James B. Hudson

Mouse cells which normally permitted polyoma virus development, and hamster cells which were non-permissive (BHK-21 and polyoma virus-transformed hamster cells), were subjected to cell-fusion techniques, and the resultant cultures were examined for the capacity of heterokaryons to yield polyoma viral capsid protein. Little or no capsid protein was synthesized in the heterokaryons, although individual mouse cells and mouse homokaryons gave normal yields. Furthermore, the hamster cell inhibitory effect manifested itself even when the mouse cells had been infected with the virus before cell fusion.


2012 ◽  
Vol 9 (1) ◽  
pp. 26 ◽  
Author(s):  
Fan Gao ◽  
Yi-Ping Wang ◽  
Qun-Ying Mao ◽  
Xin Yao ◽  
Shuang Liu ◽  
...  

2012 ◽  
Vol 9 (1) ◽  
pp. 155 ◽  
Author(s):  
Wei-Choong Ch’ng ◽  
Eric J Stanbridge ◽  
Kum-Thong Wong ◽  
Kien-Chai Ong ◽  
Khatijah Yusoff ◽  
...  

2001 ◽  
Vol 82 (6) ◽  
pp. 1517-1527 ◽  
Author(s):  
Ewa Sadowy ◽  
Marek Juszczuk ◽  
Chantal David ◽  
Bruno Gronenborn ◽  
M. Danuta Hulanicka

cDNA expression vectors of Potato leafroll virus (PLRV) were used to analyse specific mutations in the proteinase and replicase domains of the proteins encoded by ORF1 and ORF2. Agrobacterium-mediated DNA transfer was used to introduce a PLRV RNA expression unit, controlled by the 35S promoter of Cauliflower mosaic virus, into potato leaf cells. Expression of unmodified PLRV cDNA led to the replication of viral genomic and subgenomic RNAs and accumulation of the viral capsid protein, whereas alteration of amino acids GDD513–515 of the replicase to VHD abolished PLRV replication. Mutations in the presumed H-D-S catalytic triad of the viral proteinase abolished the formation of viral genomic and subgenomic RNAs as well as synthesis of the viral capsid protein. Co-agroinoculation of the GDD mutant along with any of the proteinase mutants restored virus replication in leaf discs, showing that these mutants are able to complement each other. Moreover, mutation of the postulated serine residue of the catalytic triad of the proteinase altered the pattern of proteins synthesized in vitro in comparison to wild-type, further supporting the relevance of the H-D-S motif.


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