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PMID: 7174687 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Biochemistry of terminal deoxynucleotidyl transferase. Conditions for and characterization of ultraviolet light mediated substrate cross-linking to terminal deoxynucleotidyl transferase.

The Journal of biological chemistry ·Vol. 257 ·No. 24 ·1982-12-25 ·Pages 15105-9

Modak MJ, Gillerman-Cox E

Abstract

Calf thymus terminal deoxynucleotidyl transferase may be cross-linked to substrate deoxynucleoside triphosphate as well as ATP in a reaction mediated by ultraviolet irradiation. The cross-linking requires the presence of divalent cation but is independent of primer. The cross-linking of substrate to enzyme is extremely sensitive to substrate binding site directed reagents, e.g. pyrophosphate and pyridoxal 5'-phosphate, and to o-phenanthroline, a zinc-directed chelator. The cross-linking reaction is competitively inhibited by all four deoxynucleoside triphosphates, ATP, and GTP, but is resistant to sulfhydryl reagents. When primer is provided in the reaction mixture, cross-linking of both substrate and primer to 26K subunit of terminal deoxynucleotidyl transferase may be demonstrated.

MeSH Terms
Animals Cattle DNA Nucleotidylexotransferase/metabolism,radiation effects DNA Nucleotidyltransferases/metabolism Kinetics Phosphorus Radioisotopes Protein Binding Thymus Gland/enzymology Ultraviolet Rays
Chemicals
Phosphorus Radioisotopes DNA Nucleotidyltransferases DNA Nucleotidylexotransferase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Modak M J
Gillerman-Cox E
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1982-12-25
Pages
15105-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · 1KO4-CA-00545 · United States
NCI NIH HHS · CA-21404 · United States
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