Ellman's reagent prevents dephosphorylation of histones during isolation of mitotic chromosomes

Histones H1 and H3 are highly phosphorylated in mitotic HeLa cells but are rapidly dephosphorylated by endogenous protein phosphatases during the isolation of metaphase chromosomes. We show that this dephosphorylation can be prevented by including the sulfhydryl reagent 5,5 '-dithiobis-(2-nitrobenzoate) (Ellman's reagent, or DTNB) in the isolation buffer. The minimal amount of DTNB required is approximately stoichiometric with the number of sulfhydryl groups in the lysate. Inhibition of the protein phosphatases can subsequently be reversed by treatment with dithiothreitol or 2-mercaptoethanol. DTNB is compatible with the isolation of either metaphase chromosome clusters or individual metaphase chromosomes. It should be useful in investigations of the structure and biochemistry of chromatin and chromosomes and in the study of possible functions for mitotic histone phosphorylation.

Automated summary

Histones H1 and H3 are highly phosphorylated in mitotic HeLa cells but can be prevented from dephosphorylation during the isolation of metaphase chromosomes by including the sulfhydryl reagent DTNB in the isolation buffer. The inhibition of protein phosphatases can be reversed by treatment with dithiothreitol or 2-mercaptoethanol, and DTNB is compatible with the isolation of either metaphase chromosome clusters or individual metaphase chromosomes.