TY - JOUR
T1 - High-level expression, purification and production of the fungal immunomodulatory protein-gts in baculovirus-infected insect larva
AU - Wu, Tzong Yuan
AU - Chen, Hsin-An
AU - Li, Feng Y.
AU - Lin, Ching Ting
AU - Wu, Chi Ming
AU - Hsieh, Feng Chia
AU - Tzen, Jason Tze Cheng
AU - Hsieh, Sheng Kuo
AU - Ko, Jiunn Liang
AU - Jinn, Tzyy Rong
PY - 2013/2
Y1 - 2013/2
N2 - Fip-gts, a fungal immunomodulatory protein (Fip) isolated from Ganoderma tsugae (gts), has been reported to possess therapeutic effects in the treatment of cancer and autoimmune disease. To cost-effectively produce Fip-gts and bypass the bottleneck involved in its time-consuming purification from G. tsugae, in this study, we incorporated the SPbbx secretion signal into recombinant baculovirus for expressing glycosylated and bioactive rFip-gts in baculovirus-infected insect cells and Trichoplusia ni larva. This is the first study to employ the aerosol infecting T. ni larva with recombinant baculovirus for economical and high-level production of foreign proteins. In this study, one purification could yield 10 mg of rFip-gts protein merely from ~100 infected T. ni larvae by aerosol inoculation, corresponding to 5 L (5×109 cells) of the infected Sf21 culture. In addition, the rFip-gts purified from T. ni larvae could induce the expression of interleukin-2 in murine splenocytes with an immunoresponsive level similar to that induced by LZ-8 (a known potent immunomodulatory protein purified from Ling zhi, Ganoderma lucidum). Thus, our results demonstrated that the larva-based baculovirus expression system can successfully express rFip-gts with the assembling capability required for maintaining immunomodulatory and anticancer activity. Our approach will open a new avenue for the production of rFip-gts and facilitate the immunoregulatory activity of rFip-gts available in the future.
AB - Fip-gts, a fungal immunomodulatory protein (Fip) isolated from Ganoderma tsugae (gts), has been reported to possess therapeutic effects in the treatment of cancer and autoimmune disease. To cost-effectively produce Fip-gts and bypass the bottleneck involved in its time-consuming purification from G. tsugae, in this study, we incorporated the SPbbx secretion signal into recombinant baculovirus for expressing glycosylated and bioactive rFip-gts in baculovirus-infected insect cells and Trichoplusia ni larva. This is the first study to employ the aerosol infecting T. ni larva with recombinant baculovirus for economical and high-level production of foreign proteins. In this study, one purification could yield 10 mg of rFip-gts protein merely from ~100 infected T. ni larvae by aerosol inoculation, corresponding to 5 L (5×109 cells) of the infected Sf21 culture. In addition, the rFip-gts purified from T. ni larvae could induce the expression of interleukin-2 in murine splenocytes with an immunoresponsive level similar to that induced by LZ-8 (a known potent immunomodulatory protein purified from Ling zhi, Ganoderma lucidum). Thus, our results demonstrated that the larva-based baculovirus expression system can successfully express rFip-gts with the assembling capability required for maintaining immunomodulatory and anticancer activity. Our approach will open a new avenue for the production of rFip-gts and facilitate the immunoregulatory activity of rFip-gts available in the future.
KW - Aerosol infection
KW - Baculovirus expression system
KW - Fungal immunomodulatory protein
KW - Glycoprotein
KW - Ling zhi
KW - Trichoplusia ni larva
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U2 - 10.1007/s12010-012-0049-2
DO - 10.1007/s12010-012-0049-2
M3 - Article
C2 - 23296801
AN - SCOPUS:84882945135
SN - 0273-2289
VL - 169
SP - 976
EP - 989
JO - Applied Biochemistry and Biotechnology
JF - Applied Biochemistry and Biotechnology
IS - 3
ER -