Visualizing flock house virus infection in Drosophila cells with correlated fluorescence and electron microscopy. Export

@article{citeulike:3424552, abstract = {Virus assembly occurs in a complex environment and is dependent upon viral and cellular components being properly correlated in time and space. The simplicity of the flock house virus (FHV) capsid and the extensive structural, biochemical and genetic characterization of the virus make it an excellent system for studying in vivo virus assembly. The tetracysteine motif (CCPGCC), that induces fluorescence in bound biarsenical compounds (FlAsH and ReAsH), was genetically inserted in the coat protein, to visualize this gene product during virus infection. The small size of this modification when compared to those made by traditional fluorescent proteins minimizes disruption of the coat proteins numerous functions. ReAsH not only fluoresces when bound to the tetracysteine motif but also allows correlated electron microscopy (EM) of the same cell following photoconversion and osmium staining. These studies demonstrated that the coat protein was concentrated in discrete patches in the cell. High pressure freezing (HPF) followed by freeze substitution (FS) of infected cells showed that these patches were formed by virus particles in crystalline arrays. EM tomography (EMT) of the HPF/FS prepared samples showed that these arrays were proximal to highly modified mitochondria previously established to be the site of RNA replication. Two features of the mitochondrial modification are approximately 60 nm spherules that line the outer membrane and the large chamber created by the convolution induced in the entire organelle.}, author = {Lanman, J. and Crum, J. and Deerinck, T. J. and Gaietta, G. M. and Schneemann, A. and Sosinsky, G. E. and Ellisman, M. H. and Johnson, J. E.}, citeulike-article-id = {3424552}, citeulike-linkout-0 = {http://dx.doi.org/10.1016/j.jsb.2007.09.009}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/17998167}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=17998167}, doi = {10.1016/j.jsb.2007.09.009}, issn = {1095-8657}, journal = {Journal of structural biology}, keywords = {clem, dab, em, fluorescence, hiv, hpf, microscopy, photoconvert, reash, tetracysteine}, month = {March}, number = {3}, pages = {439--446}, posted-at = {2008-10-17 14:59:31}, priority = {2}, title = {Visualizing flock house virus infection in Drosophila cells with correlated fluorescence and electron microscopy.}, url = {http://dx.doi.org/10.1016/j.jsb.2007.09.009}, volume = {161}, year = {2008} }

TY - JOUR ID - citeulike:3424552 L3 - citeulike-article-id:3424552 N2 - Virus assembly occurs in a complex environment and is dependent upon viral and cellular components being properly correlated in time and space. The simplicity of the flock house virus (FHV) capsid and the extensive structural, biochemical and genetic characterization of the virus make it an excellent system for studying in vivo virus assembly. The tetracysteine motif (CCPGCC), that induces fluorescence in bound biarsenical compounds (FlAsH and ReAsH), was genetically inserted in the coat protein, to visualize this gene product during virus infection. The small size of this modification when compared to those made by traditional fluorescent proteins minimizes disruption of the coat proteins numerous functions. ReAsH not only fluoresces when bound to the tetracysteine motif but also allows correlated electron microscopy (EM) of the same cell following photoconversion and osmium staining. These studies demonstrated that the coat protein was concentrated in discrete patches in the cell. High pressure freezing (HPF) followed by freeze substitution (FS) of infected cells showed that these patches were formed by virus particles in crystalline arrays. EM tomography (EMT) of the HPF/FS prepared samples showed that these arrays were proximal to highly modified mitochondria previously established to be the site of RNA replication. Two features of the mitochondrial modification are approximately 60 nm spherules that line the outer membrane and the large chamber created by the convolution induced in the entire organelle. IS - 3 JF - Journal of structural biology SN - 1095-8657 EP - 446 TI - Visualizing flock house virus infection in Drosophila cells with correlated fluorescence and electron microscopy. VL - 161 SP - 439 KW - clem KW - dab KW - em KW - fluorescence KW - hiv KW - hpf KW - microscopy KW - photoconvert KW - reash KW - tetracysteine AU - Lanman, J AU - Crum, J AU - Deerinck, TJ AU - Gaietta, GM AU - Schneemann, A AU - Sosinsky, GE AU - Ellisman, MH AU - Johnson, JE PY - 2008/03// UR - http://dx.doi.org/10.1016/j.jsb.2007.09.009 ER -