2001Zhonghua weishengwuxue he mianyixue zazhiRequires access

Gene cloning and expression of hybrid HPV6b L1/16E7 protein in insect cells

Zhao Kongnan

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Abstract

Objective In order to make the genetic engineering vaccine against CA and cervical cancer, the hybrid HPV6b L1/16E7 protein was expressed in Sf 9 insect cells with baculovirus express vector system. Methods The gene fragment of hybrid HPV6b L1/16E7 has been amplified by PCR and cloned into the baculovirus transfer vector pVL1393, a recombinant baculovirus expression vector was constructed to express the hybrid HPV6b L1/16E7 gene in insect cells. Results The hybrid HPV6b L1/16E7 protein was expressed in Sf 9 insect cells, assembled into virus like particles (VLPs). Conclusion The hybrid HPV6b L1/16E7 VLPs expressed in Sf 9 insect cells is quite potential in the future research, mechanism of HPV infection, for the development of genetic engineering vaccine.

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What this paper is about

Objective In order to make the genetic engineering vaccine against CA and cervical cancer, the hybrid HPV6b L1/16E7 protein was expressed in Sf 9 insect cells with baculovirus express vector system. Methods The gene fragment of hybrid HPV6b L1/16E7 has been amplified by PCR and cloned into the baculovirus transfer vector pVL1393, a recombinant baculovirus expression vector was constructed to express the hybrid HPV6b L1/16E7 gene in insect cells. Results The hybrid HPV6b L1/16E7 protein was expressed in Sf 9 insect cells, assembled into virus like particles (VLPs). Conclusion The hybrid HPV6b L1/16E7 VLPs expressed in Sf 9 insect cells is quite potential in the future research, mechanism of HPV infection, for the development of genetic engineering vaccine.

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Available abstract

Objective In order to make the genetic engineering vaccine against CA and cervical cancer, the hybrid HPV6b L1/16E7 protein was expressed in Sf 9 insect cells with baculovirus express vector system. Methods The gene fragment of hybrid HPV6b L1/16E7 has been amplified by PCR and cloned into the baculovirus transfer vector pVL1393, a recombinant baculovirus expression vector was constructed to express the hybrid HPV6b L1/16E7 gene in insect cells. Results The hybrid HPV6b L1/16E7 protein was expressed in Sf 9 insect cells, assembled into virus like particles (VLPs). Conclusion The hybrid HPV6b L1/16E7 VLPs expressed in Sf 9 insect cells is quite potential in the future research, mechanism of HPV infection, for the development of genetic engineering vaccine.

Key concepts: Cloning (programming), Gene, Biology, Vector (molecular biology), Recombinant DNA, Molecular biology, Virology, Expression vector

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