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Published June 2009 | Accepted Version + Published
Journal Article Open

Nanogold as a specific marker for electron cryotomography

Abstract

While electron cryotomography (ECT) provides "molecular" resolution, three-dimensional images of unique biological specimens, sample crowdedness, and/or resolution limitations can make it difficult to identify specific macromolecular components. Here we used a 1.4 nm Nanogold® cluster specifically attached to the Fc fragment of IgG to monitor its interaction with the neonatal Fc receptor (FcRn), a membrane-bound receptor that transports IgG across cells in acidic intracellular vesicles. ECT was used to image complexes formed by Nanogold-labeled Fc bound to FcRn attached to the outer surface of synthetic liposomes. In the resulting three-dimensional reconstructions, 1.4 nm Nanogold particles were distributed predominantly along the interfaces where 2:1 FcRn-Fc complexes bridged adjacent lipid bilayers. These results demonstrate that the 1.4 nm Nanogold cluster is visible in tomograms of typically thick samples (250 nm) recorded with defocuses appropriate for large macromolecules and is thus an effective marker.

Additional Information

© 2009 Microscopy Society of America. Received December 17, 2008; accepted April 3, 2009. We thank Noreen Tiangco for preparing Nanogold-Fc, William Tivol for the help with microscopy, and members of the Bjorkman and Jensen laboratories for helpful suggestions. This work was supported by a postdoctoral fellowship from the Cancer Research Institute (Y.H.), the National Institutes of Health (2 R37 AI041239-06A1 to P.J.B.), and gifts to Caltech to support electron microscopy from the Gordon and Betty Moore Foundation and the Agouron Institute.

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Published - He2009p4574Microscopy_and_Microanalysis.pdf

Accepted Version - nihms-157152.pdf

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