کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1179477 962779 2006 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Reversible resolution of flavin and pterin cofactors of His-tagged Escherichia coli DNA photolyase
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Reversible resolution of flavin and pterin cofactors of His-tagged Escherichia coli DNA photolyase
چکیده انگلیسی

Escherichia coli photolyase catalyzes the repair of cyclobutane pyrimidine dimers (CPD) in DNA under near UV/blue-light irradiation. The enzyme contains flavin adenine dinucleotide (FAD) and methenyltetrahydrofolate (MTHF) as noncovalently bound light sensing cofactors. To study the apoprotein–chromophore interactions we developed a new procedure to prepare apo-photolyase. MTHF-free photolyase was obtained by binding the C-terminal His-tagged holoenzyme to a metal-affinity column at neutral pH and washing the column with deionized water. Under these conditions the flavin remains bound and the defolated enzyme can be released from the column with 0.5 M imidazole pH 7.2. The MTHF-free protein was still capable of DNA repair, showing 70% activity of native enzyme. Fluorescence polarization experiments confirmed that MTHF binding is weakened at low ionic strength. Apo-photolyase was obtained by treating the His-tagged holoenzyme with 0.5 M imidazole pH 10.0. The apo-photolyase thus obtained was highly reconstitutable and bound nearly stoichiometric amounts of FADox. Photolyase reconstituted with FADox had about 34% activity of native enzyme, which increased to 83% when FADox was reduced to FADH−. Reconstitution kinetics performed at 20 °C showed that apo-photolyase associates with FADH− much faster (kobs ∼ 3000 M− 1 s− 1) than with FADox (kobs = 34 M− 1 s− 1). The dissociation constant of the photolyase–FADox complex is about 2.3 μM and that of E-FADH− is not higher than 20 nM (pH 7.2).

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics - Volume 1764, Issue 9, September 2006, Pages 1454–1461
نویسندگان
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