Paulson J R
Eur J Biochem. 1980 Oct;111(1):189-97. doi: 10.1111/j.1432-1033.1980.tb06092.x.
It has been shown by D'Anna et al. [Nucleic Acids Res. 5, 3195-3207 (1978)] that histones H1 and H3, which are highly phosphorylated during mitosis in mammalian cells, become rapidly dephosphorylated during conventional metaphase chromosome isolation procedures. We show here that this dephosphorylation can be completely prevented by including sulfhydryl reagents, such as p-chloromercuriphenyl sulfonate or 5,5'-dithiobis(2-nitrobenzoate), in the chromosome isolation buffers. These reagents also efficiently inhibit the endogenous proteases present in isolated HeLa chromosomes and nuclei.
D'Anna等人[《核酸研究》5, 3195 - 3207 (1978)]已表明,在哺乳动物细胞有丝分裂期间高度磷酸化的组蛋白H1和H3,在常规中期染色体分离过程中会迅速去磷酸化。我们在此表明,通过在染色体分离缓冲液中加入巯基试剂,如对氯汞苯磺酸盐或5,5'-二硫代双(2-硝基苯甲酸),可以完全防止这种去磷酸化。这些试剂还能有效抑制分离的HeLa染色体和细胞核中存在的内源性蛋白酶。