Construction of chimera protein by using artificial restriction DNA cutter.

Akihiko Uehara, Yoji Yamamoto, Akira Watanabe, Hiroyuki Aburatani, Makoto Komiyama
Author Information
  1. Akihiko Uehara: Research Center for Advanced Science and Technology, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, 153-8904, Japan.

Abstract

We have already developed artificial restriction DNA cutter (ARCUT), which can hydrolyze double-stranded DNA site-selectively, by using Ce(IV)/EDTA in combination with two pseudo-complementary peptide nucleic acids (pcPNAs). Here, ARCUT was used to prepare a chimera protein. The gene for WW-domain containing oxidoreductase (WWOX) was clipped off by ARCUT just before its stop codon, and ligated with the gene for enhanced green fluorescent protein (EGFP). Conventional PCR for insertion of restriction enzyme site is never required.

MeSH Term

Animals
COS Cells
Cerium
Chlorocebus aethiops
DNA Restriction Enzymes
DNA, Recombinant
Deoxyribonucleases
Edetic Acid
Green Fluorescent Proteins
Hydrolysis
Oxidoreductases
Peptide Nucleic Acids
Recombinant Fusion Proteins

Chemicals

DNA, Recombinant
Peptide Nucleic Acids
Recombinant Fusion Proteins
enhanced green fluorescent protein
Green Fluorescent Proteins
Cerium
Edetic Acid
Oxidoreductases
Deoxyribonucleases
DNA Restriction Enzymes

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