Expression of Immunologically Active Porcine Recombinant TGF-${\beta}1$ Precursor Protein in Baculovirus System

  • Lim, Hyun (Department of Microbiology, College of Natural Sciences, Kangwon National University) ;
  • Kim, Pyeung-Hyeun (Department of Microbiology, College of Natural Sciences, Kangwon National University) ;
  • Chun, Gie-Taek (Department of Microbiology, College of Natural Sciences, Kangwon National University) ;
  • Choi, Eui-Yul (Department of Genetic Engineering, College of Natural Sciences, Hallym University) ;
  • Yie, Se-Won (Department of Microbiology, College of Natural Sciences, Kangwon National University)
  • Published : 1997.01.01

Abstract

In order to express recombinant porcine TGF-${\beta}1$ protein in a baculovirus expression system the entire TGF-${\beta}1$gene containing extra amino acids at the N terminus was cloned into pFBa and pFBb of the Bac-To-$Bac^{TM}$ baculovirus expression system. One of the clones contained 106 extra amino acids and was designated pFBa-106 TGF-${\beta}1$, and the other had 28 extra amino acids and was designated pFBb-28 TGF-${\beta}1$. The orientation of the gene was identified with restriction enzyme mapping and PCR with internal TGF-${\beta}1$ primers. Sf-9 cells were infected at a m.o.i. of 10 by the recombinant viruses generated from the two expected sizes of 55 kD and 46.4kD. these precursor forms of TGF-${\beta}1$ with a polyclonal antibody against human TGF-${\beta}1$. No mature form of TGF-${\beta}1$ protein was detected on SDS gels and an immunoblot indicated that TGF-${\beta}1$ precursor is not properlu processed in insect cells.

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