کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1993952 1064721 2010 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Measurement of kinetic parameters of human platelet DNA polymerase γ
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Measurement of kinetic parameters of human platelet DNA polymerase γ
چکیده انگلیسی

Synthesis of mitochondrial DNA is performed by DNA polymerase γ. Mutations in POLG, the gene encoding the catalytic subunit of DNA polymerase γ, are a major cause of neurological disease. A large proportion of patients carry rare nucleotide substitutions leading to single amino acid changes. Confirming that these replacements are pathogenic can be problematic without biochemical evidence. Here, we provide a hands-on protocol for an in vitro kinetic assay of DNA polymerase γ which allows assessment of the Km and Vmax for the incoming nucleotide of the polymerization reaction. To avoid measurement of contaminating nuclear DNA polymerases, platelet extracts are used since platelets do not contain a nucleus. Moreover, platelets have the advantage of being obtainable relatively non-invasively. Polymerization activity is determined by measurement of the incorporation of radioactive thymidine 5′-triphosphate (dTTP) on the homopolymeric RNA substrate poly(rA)·oligo(dT)12–18. To further minimize nuclear DNA polymerase activity, aphidicolin, an inhibitor of most nuclear DNA polymerases, is included in the reaction. In addition, reactions are carried out in the absence and presence of the competitive inhibitor of DNA polymerase γ, 2′,3′-dideoxythymidine 5′-triphosphate (ddTTP), to allow calculation of the ddTTP-sensitive incorporation. With this method, platelets from healthy control subjects extracted with 3% Triton X-100 showed a Km for dTTP of 1.42 μM and a Vmax of 0.83 pmol min−1 mg−1.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Methods - Volume 51, Issue 4, August 2010, Pages 374–378
نویسندگان
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