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. 2008 Jun;19(6):1124-6.
doi: 10.1021/bc700480j. Epub 2008 May 29.

Strategy for efficient site-specific FRET-dye labeling of ubiquitin

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Strategy for efficient site-specific FRET-dye labeling of ubiquitin

Michael Wen-Pin Kao et al. Bioconjug Chem. 2008 Jun.

Abstract

To study conformational changes within a single protein molecule, sp-FRET (single pair fluorescence resonance energy transfer) is an important technique to provide distance information. However, incorporating donor and acceptor dyes into the same protein molecule is not an easy task. Here, we report a strategy for the efficient double-labeling of a protein on a solid support. An ubiquitin mutant with two Cys mutations, one with high solvent accessibility and the other with low solvent accessibility, was constructed. The protein was bound to magnetic beads and reacted with the dyes. The first dye reacted with the side-chain of the Cys with the high solvent accessibility and the second with the other Cys under partially denaturing conditions. Using this method, we can easily label two dyes in a site-specific way on ubiquitin with a satisfied yield. The labeling sites for donor and acceptor dyes can be easily swapped.

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