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The role of the gulose-mannose part of bleomycin in activation of iron-molecular oxygen complexes

Authors :
Kénani, A
Bailly, C
Helbecque, N
Catteau, J P
Houssin, R
Bernier, J L
Hénichart, J P
Source :
Biochemical Journal; July 1988, Vol. 253 Issue: 2 p497-504, 8p
Publication Year :
1988

Abstract

A comparison of the complexing properties of metal ions and O2 activation by bleomycin-A2 (BLM-A2) and deglyco-BLM-A2 is presented. Deglyco-BLM-A2 is obtained from the parent derivative by HF cleavage of the sugar moiety followed by h.p.l.c. purification. Complexing of Cu(II) and Fe(III) is studied by using c.d. and e.s.r. spectroscopy. Spin-trapping experiments in the presence of phenyl N-t-butylnitrone indicated lower production of free radicals by deglyco-BLM-A2. Finally, a proposal is made to explain this discrepancy, focusing on the probable role of the gulose-mannose moiety acting as a protecting pocket, comparable with the pocket and picket-fence porphyrins described for haemoproteins.

Details

Language :
English
ISSN :
02646021 and 14708728
Volume :
253
Issue :
2
Database :
Supplemental Index
Journal :
Biochemical Journal
Publication Type :
Periodical
Accession number :
ejs51301851
Full Text :
https://doi.org/10.1042/bj2530497