Improved detection of terminal transferase (TdT): the use of detergents on glutaraldehyde-fixed non-dehydrated cells prevents denaturation and diffusion artifacts

Leuk Res. 1986;10(8):1041-9. doi: 10.1016/0145-2126(86)90257-2.

Abstract

TdT as an intranuclear enzyme mainly of immature lymphoid cells is commonly determined immunologically using air-dried cell smears fixed with methanol. Both cell dehydration and alcohol fixation were found here to denature TdT and surface antigens. This could be prevented by using non-dehydrated cells bound electrostatically to poly-L-lysine-coated slides, fixed minimally with glutaraldehyde and rendered permeable to antibodies by the non-ionic detergent Brij 56. Crosslinking glutaraldehyde in addition prevented diffusion of TdT to extranuclear sites. By avoiding artifacts of denaturation and diffusion, a higher sensitivity in the detection of TdT was achieved despite considerably lower quantities of antibody.

MeSH terms

  • Cell Membrane Permeability
  • DNA Nucleotidylexotransferase / analysis*
  • DNA Nucleotidyltransferases / analysis*
  • Detergents / pharmacology*
  • Diffusion
  • Glutaral
  • Histocytochemistry
  • Humans
  • Leukemia / enzymology
  • Methods
  • Protein Denaturation
  • Surface-Active Agents / pharmacology*
  • T-Lymphocytes / enzymology

Substances

  • Detergents
  • Surface-Active Agents
  • DNA Nucleotidyltransferases
  • DNA Nucleotidylexotransferase
  • Glutaral