TY - JOUR
T1 - Secretory production system of bionanocapsules using a stably transfected insect cell line
AU - Shishido, Takuya
AU - Muraoka, Masaru
AU - Ueda, Masakazu
AU - Seno, Masaharu
AU - Tanizawa, Katsuyuki
AU - Kuroda, Shun'ichi
AU - Fukuda, Hideki
AU - Kondo, Akihiko
N1 - Funding Information:
Acknowledgements This study was supported by grants-in-aid for Research on Advanced Medical Technology from the Ministry of Health, Labour and Welfare.
PY - 2006/12
Y1 - 2006/12
N2 - Bionanocapsules (BNCs) are hollow nanoscale particles composed of L protein of the hepatitis B virus surface antigen that represent specific affinity for human hepatocytes. BNCs can transfer genes and drugs into human hepatocytes efficiently and specifically. BNC can be expressed in yeast cells. In this study, we developed a new L particle production system using a stably transfected insect cell line. For this purpose, we established a host-vector system using the Trichoplusia ni insect cell line. L particles were efficiently secreted by the overexpression of the L protein, which was fused to the secretion signal peptide. The concentration of L particles was reached approximately 1.7 μg/ml in 5 days during cultivation in a serum-free medium without antibiotic selective pressure. The production of L particles was maintained for at least 75 days. The secretory production of L particles facilitated their easy purification by chromatography. Furthermore, it was demonstrated that purified L particles can transfect only human hepatocytes. Therefore, an insect cell expression system is an attractive tool for the production of BNC.
AB - Bionanocapsules (BNCs) are hollow nanoscale particles composed of L protein of the hepatitis B virus surface antigen that represent specific affinity for human hepatocytes. BNCs can transfer genes and drugs into human hepatocytes efficiently and specifically. BNC can be expressed in yeast cells. In this study, we developed a new L particle production system using a stably transfected insect cell line. For this purpose, we established a host-vector system using the Trichoplusia ni insect cell line. L particles were efficiently secreted by the overexpression of the L protein, which was fused to the secretion signal peptide. The concentration of L particles was reached approximately 1.7 μg/ml in 5 days during cultivation in a serum-free medium without antibiotic selective pressure. The production of L particles was maintained for at least 75 days. The secretory production of L particles facilitated their easy purification by chromatography. Furthermore, it was demonstrated that purified L particles can transfect only human hepatocytes. Therefore, an insect cell expression system is an attractive tool for the production of BNC.
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U2 - 10.1007/s00253-006-0486-3
DO - 10.1007/s00253-006-0486-3
M3 - Article
C2 - 16847600
AN - SCOPUS:34447273920
SN - 0175-7598
VL - 73
SP - 505
EP - 511
JO - Applied Microbiology and Biotechnology
JF - Applied Microbiology and Biotechnology
IS - 3
ER -