TY - JOUR
T1 - Determination of methylation specificity of sequence-specific DNA methyltransferases using matrix assisted laser desorption/ionization time-of-flight mass spectrometry
AU - Tamura, Takashi
AU - Araki, Yoshinori
AU - Yamaoka, Seiji
AU - Inagaki, Kenji
AU - Tanaka, Hidehiko
N1 - Funding Information:
The authors are grateful to the MALDI-TOF MS laboratory of the Graduate School of Okayama University for the molecular mass analysis. This work was supported in part by a grant-in-aid for Scientific Research (07680688) from the Ministry of Education, Science and Culture of Japan to K.I.
PY - 1997/10/15
Y1 - 1997/10/15
N2 - We describe here a sensitive and straightforward method for characterizing the methylation specificity of type II DNA methyltransferase (MTase) using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. DNA substrate, prepared by ligation of a commercially available oligonucleotide, was modified by the subject MTase, and was derivatized to a mixture of single-stranded oligonucleotides through endonuclease treatment, heat-denaturation and limited digestion by 3'-terminus-specific phosphodiesterase I. MALDI-TOF mass spectrometry was used to determine the mass differences between the digestion products, and the methylated nucleotide was explicitly identified by the mass increase of 14 Da due to the base modification. The method was applicable to the three representative MTases M.EcoRI, M.BamHI and M.HaeIII.
AB - We describe here a sensitive and straightforward method for characterizing the methylation specificity of type II DNA methyltransferase (MTase) using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. DNA substrate, prepared by ligation of a commercially available oligonucleotide, was modified by the subject MTase, and was derivatized to a mixture of single-stranded oligonucleotides through endonuclease treatment, heat-denaturation and limited digestion by 3'-terminus-specific phosphodiesterase I. MALDI-TOF mass spectrometry was used to determine the mass differences between the digestion products, and the methylated nucleotide was explicitly identified by the mass increase of 14 Da due to the base modification. The method was applicable to the three representative MTases M.EcoRI, M.BamHI and M.HaeIII.
UR - http://www.scopus.com/inward/record.url?scp=0030841333&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0030841333&partnerID=8YFLogxK
U2 - 10.1093/nar/25.20.4162
DO - 10.1093/nar/25.20.4162
M3 - Short survey
C2 - 9321674
AN - SCOPUS:0030841333
SN - 0305-1048
VL - 25
SP - 4162
EP - 4164
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 20
ER -