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Supramolecular latching system based on ultrastable synthetic binding pairs as versatile tools for protein imaging.


ABSTRACT: Here we report ultrastable synthetic binding pairs between cucurbit[7]uril (CB[7]) and adamantyl- (AdA) or ferrocenyl-ammonium (FcA) as a supramolecular latching system for protein imaging, overcoming the limitations of protein-based binding pairs. Cyanine 3-conjugated CB[7] (Cy3-CB[7]) can visualize AdA- or FcA-labeled proteins to provide clear fluorescence images for accurate and precise analysis of proteins. Furthermore, controllability of the system is demonstrated by treating with a stronger competitor guest. At low temperature, this allows us to selectively detach Cy3-CB[7] from guest-labeled proteins on the cell surface, while leaving Cy3-CB[7] latched to the cytosolic proteins for spatially conditional visualization of target proteins. This work represents a non-protein-based bioimaging tool which has inherent advantages over the widely used protein-based techniques, thereby demonstrating the great potential of this synthetic system.

SUBMITTER: Kim KL 

PROVIDER: S-EPMC5923385 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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Supramolecular latching system based on ultrastable synthetic binding pairs as versatile tools for protein imaging.

Kim Kyung Lock KL   Sung Gihyun G   Sim Jaehwan J   Murray James J   Li Meng M   Lee Ara A   Shrinidhi Annadka A   Park Kyeng Min KM   Kim Kimoon K  

Nature communications 20180427 1


Here we report ultrastable synthetic binding pairs between cucurbit[7]uril (CB[7]) and adamantyl- (AdA) or ferrocenyl-ammonium (FcA) as a supramolecular latching system for protein imaging, overcoming the limitations of protein-based binding pairs. Cyanine 3-conjugated CB[7] (Cy3-CB[7]) can visualize AdA- or FcA-labeled proteins to provide clear fluorescence images for accurate and precise analysis of proteins. Furthermore, controllability of the system is demonstrated by treating with a stronge  ...[more]

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