posted on 2006-03-01, 00:00authored byChristopher J. Ackerson, Pablo D. Jadzinsky, Grant J. Jensen, Roger D. Kornberg
A general method of rigid, specific labeling of proteins with gold clusters has been devised. The
method relies on the conjugation of a glutathione monolayer-protected gold cluster (MPC) with a single
chain Fv antibody fragment (scFv), mutated to present an exposed cysteine residue. Efficient formation of
a gold−thiolate bond between the MPC and scFv depends on activation of the gold cluster by chemical
oxidation. Once formed, the MPC−scFv conjugate is treated with a reductant to quench cluster reactivity.
The procedure has been performed with an MPC with an average Au71 core and an scFv directed against
a tetrameric protein, the influenza neuraminidase. A complex of the MPC−scFv conjugate with the
neuraminidase was isolated, and the presence of four gold clusters was verified by cryoelectron microscopy.