Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10533074 | Analytical Biochemistry | 2005 | 9 Pages |
Abstract
A new strategy for dual site-selective labeling of proteins that uses metabolically incorporated selenomethionine as a target for covalent modification by iodoacetamide derivatives, forming selenonium salts, is described. In the absence of free cysteine, labeling is specific and efficient. Dual-targeted labeling of a protein can be achieved with combinations of unique cysteine and methionine residues, if the cysteine is labeled first with a maleimide or another reagent that does not react with the selenomethionine. The method should be useful in biophysical applications such as fluorescence energy transfer.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Shenhui Lang, Donald E. Spratt, J. Guy Guillemette, Michael Palmer,