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A Covalently Linked 10 Nm Gold Immunoprobe

Published online by Cambridge University Press:  02 July 2020

Edmund Gutierrez ,
Richard D. Powell ,
James F. Hainfeld  and
Peter M. Takvorian
Edmund Gutierrez
Affiliation:
Nanoprobes, Incorporated, Stony Brook, NY11790.
Richard D. Powell
Affiliation:
Nanoprobes, Incorporated, Stony Brook, NY11790.
James F. Hainfeld
Affiliation:
Biology Department, Brookhaven National Laboratory, Upton, NY11973
Peter M. Takvorian
Affiliation:
Biological Sciences Department, Rutgers University, Newark, NJ07102.
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Extract

Chemically functionalized metal cluster compounds have demonstrated important advantages over colloidal gold as biological microscopy labels. They are covalently cross-linked to the targeting biomolecule, and therefore may be conjugated to a wide range of molecules which cannot be labeled with colloidal gold. The 1.4 nm Nanogold® cluster has been conjugated to peptides, lipids and oligonucleotides, some of which have been proposed as elements of novel molecular wires and novel materials. Dissociation of colloidal gold particles from the conjugate probe, a source of error in quantitative immunogold studies, is greatly reduced by covalent cross-linking. Nanogold® is an uncharged molecule, and because its surface is completely coordinated by organic ligands, nonspecific binding is greatly reduced. Nanogold® conjugates also show greatly enhanced penetration into cells and tissue sections. However, gold probes larger than Nanogold® are desirable for improved visualization in specimens with electron-dense regions or staining, or for applications such as double labeling studies with different sized gold labels, or visualizing wider antigen distributions.

Type
Cytochemistry
Information
Microscopy and Microanalysis , Volume 5 , Issue S2: Proceedings: Microscopy & Microanalysis '99, Microscopy Society of America 57th Annual Meeting, Microbeam Analysis Society 33rd Annual Meeting, Portland, Oregon August 1-5, 1999 , August 1999 , pp. 1324 - 1325
Copyright
Copyright © Microscopy Society of America

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References

1.Gregori, L., et al., J. Biol. Chem., 272 (1997) 58.CrossRefGoogle Scholar
2.Adler-Moore, J., Bone Marrow Transplantation, 14 (1994) S3.Google Scholar
3.Alivisatos, A. P., et al., Nature, 382 (1996) 609.CrossRefGoogle Scholar
4.Behnke, O., et al., Eur. J. Cell Biol., 41 (1986) 326.Google Scholar
5.Hainfeld, J. F., Proc. XIIInt. Cong. Elec. Microsc.(1990) p. 954–955.Google Scholar
6.Takizawa, T., and Robinson, J. O., J. Histochem. Cytochem., 43 (1994) 1615.CrossRefGoogle Scholar
7.Slot, J. W., and Geuze, H. J., Eur. J. Cell Biol, 38 (1985) 8.Google Scholar
8.Ths work was partly supported by SBIR grant number R44 GM50048.Google Scholar