Production and characterization of murine monoclonal anti-human DNase II antibodies, and their use for immunoaffinity purification of DNase II from human liver and urine

• Published in: Biochimica et biophysica acta Vol. 1570; no. 3; pp. 160 - 164
• Main Authors: Nakajima, Tamiko, Yasuda, Toshihiro, Takeshita, Haruo, Mori, Shinjiro, Mogi, Kouichi, Kaneko, Yasushi, Nakazato, Emiko, Kishi, Koichiro
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15.04.2002
• Subjects: Animals; Antibodies, Monoclonal; Chromatography; Chromatography, Affinity; DNase II; Electrophoresis, Polyacrylamide Gel; Endodeoxyribonucleases - chemistry; Endodeoxyribonucleases - immunology; Female; Human; Humans; Immunoaffinity; Liver; Liver - chemistry; Mice; Mice, Inbred BALB C; Monoclonal antibody; Murine; Purification; Rabbits; Urine; Human; Urine; Purification; Immunoaffinity; Liver; DNase II; Monoclonal antibody; Murine; Chromatography
• ISSN: 0304-4165; 0006-3002; 1872-8006
• DOI: 10.1016/S0304-4165(02)00191-5

Four murine monoclonal anti-human deoxyribonuclease II (DNase II) antibodies were obtained from BALB/c mice immunized with human DNase II purified from human liver. Both single radial enzyme diffusion (SRED) and DNA-cast polyacrylamide gel electrophoresis (DNA-cast PAGE) were very useful for obtaining the DNase II-specific antibodies. All of the antibodies showed specific inhibition of human DNase II enzyme activity and specific immunostaining of the 32-kDa enzyme band, which is one of the three non-identical subunits of human DNase II molecule separated by sodium dodecyl sulfate (SDS)-PAGE followed by blotting on a transfer membrane. A formyl-cellulofine resin conjugated with each antibody specifically adsorbed and efficiently desorbed the active DNase II enzyme. Insertion of the immunoaffinity step in our purification procedure made the purification of human DNase II easier, faster and more effective than the conventional procedure.