Background: Thiol-mediated redox regulation of proteins plays a key role in many cellular processes.
Methods: To understand the redox status of cysteinyl thiol groups of the desired proteins, we developed a new maleimide reagent: a maleimide-conjugated single strand DNA, DNA-maleimide (DNA-Mal).
Results: DNA-Mal labelled proteins run as a distinct band on SDS-PAGE, with a discrete 9.32 kDa mobility shift per label regardless of the protein species or electrophoretic conditions.
Conclusions: DNA-Mal labels free thiols like standard maleimide reagents, but possesses practical advantages in titration of the number and relative content of free thiols in a protein.
General significance: The versatility of DNA molecule enhances the application of DNA-Mal in a broader range of cysteine containing proteins.
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