Title of article :
Use of Trinitrobenzensulfonate for Affinity Labeling of Lysine Residues at Phosphate Binding Sites of Some Enzymes
Author/Authors :
Hanau، نويسنده , , S. and Dallocchio، نويسنده , , F. and Rippa، نويسنده , , M.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1993
Pages :
4
From page :
218
To page :
221
Abstract :
Trinitrobenzensulfonate, a reagent for lysine residues, inactivates lamb liver 6-phosphogluconate dehydrogenase through affinity labeling. Complete inactivation is due to the binding of only one residue of reagent per enzyme subunit. Other enzymes with a phosphate binding site are also inactivated by affinity labeling. It appears that trinitrobenzensulfonate, when used at low concentrations, first binds to a phosphate binding site, then reacts with a nearby lysine residue. This reagent presents some advantages over pyridoxal phosphate, which has similar characteristics.
Journal title :
Archives of Biochemistry and Biophysics
Serial Year :
1993
Journal title :
Archives of Biochemistry and Biophysics
Record number :
1450252
Link To Document :
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