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Quantum dot targeting with lipoic acid ligase and HaloTag for single-molecule imaging on living cells.


ABSTRACT: We present a methodology for targeting quantum dots to specific proteins on living cells in two steps. In the first step, Escherichia coli lipoic acid ligase (LplA) site-specifically attaches 10-bromodecanoic acid onto a 13 amino acid recognition sequence that is genetically fused to a protein of interest. In the second step, quantum dots derivatized with HaloTag, a modified haloalkane dehalogenase, react with the ligated bromodecanoic acid to form a covalent adduct. We found this targeting method to be specific, fast, and fully orthogonal to a previously reported and analogous quantum dot targeting method using E. coli biotin ligase and streptavidin. We used these two methods in combination for two-color quantum dot visualization of different proteins expressed on the same cell or on neighboring cells. Both methods were also used to track single molecules of neurexin, a synaptic adhesion protein, to measure its lateral diffusion in the presence of neuroligin, its trans-synaptic adhesion partner.

SUBMITTER: Liu DS 

PROVIDER: S-EPMC3528850 | biostudies-literature | 2012 Dec

REPOSITORIES: biostudies-literature

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Quantum dot targeting with lipoic acid ligase and HaloTag for single-molecule imaging on living cells.

Liu Daniel S DS   Phipps William S WS   Loh Ken H KH   Howarth Mark M   Ting Alice Y AY  

ACS nano 20121205 12


We present a methodology for targeting quantum dots to specific proteins on living cells in two steps. In the first step, Escherichia coli lipoic acid ligase (LplA) site-specifically attaches 10-bromodecanoic acid onto a 13 amino acid recognition sequence that is genetically fused to a protein of interest. In the second step, quantum dots derivatized with HaloTag, a modified haloalkane dehalogenase, react with the ligated bromodecanoic acid to form a covalent adduct. We found this targeting meth  ...[more]

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