Tetrairidium, a Four-Atom Cluster, Is Readily Visible as a Density Label in Three-Dimensional Cryo-EM Maps of Proteins at 10–25 Å Resolution
Heavy metal clusters derivatized to bind to designated chemical groups on proteins have great potential as density labels for cryo-electron microscopy. Smaller clusters offer higher resolution and penetrate more easily into sterically restricted sites, but are more difficult to detect. In this conte...
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Veröffentlicht in: | Journal of structural biology 1999-09, Vol.127 (2), p.169-176 |
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Zusammenfassung: | Heavy metal clusters derivatized to bind to designated chemical groups on proteins have great potential as density labels for cryo-electron microscopy. Smaller clusters offer higher resolution and penetrate more easily into sterically restricted sites, but are more difficult to detect. In this context, we have explored the potential of tetrairidium (Ir4) as a density label by attaching it via maleimide linkage to the C-terminus of the hepatitis B virus (HBV) capsid protein. Although the clusters are not visible in unprocessed cryo-electron micrographs, they are distinctly visible in three-dimensional density maps calculated from them, even at only partial occupancy. The Ir4 label was clearly visualized in our maps at 11–14 Å resolution of both size variants of the HBV capsid, thus confirming our previous localization of this site with undecagold (Zlotnick, A., Cheng, N., Stahl, S. J., Conway, J. F., Steven, A. C., and Wingfield, P. T., Proc. Natl. Acad. Sci. USA 94, 9556–9561, 1997). Ir4 penetrated to the interior of intact capsids to label this site on their inner surface, unlike undecagold for which labelling was achieved only with dissociated dimers that were then reassembled into capsids. The Ir4 cluster remained visible as the resolution of the maps was lowered progressively to ∼25 Å. |
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ISSN: | 1047-8477 1095-8657 |
DOI: | 10.1006/jsbi.1999.4120 |