Purification and characterization of virus-like particles and pentamers produced by the expression of SV40 capsid proteins in insect cells

• Published in: Biochimica et biophysica acta 1996-05, Vol.1290 (1), p.37-45
• Main Authors: Kosukegawa, A, Arisaka, F, Takayama, M, Yajima, H, Kaidow, A, Handa, H
• Format: Article
• Language: English
• Subjects: Analytical ultracentrifugation; Animals; Baculoviridae - genetics; Biopolymers; Capsid - genetics; Cell Line; Cloning, Molecular; Dithiothreitol; Egtazic Acid; Microscopy, Electron; Recombinant baculovirus; Reconstitution, in vitro; Simian virus 40 - genetics; Spodoptera; SV40; Ultracentrifugation; Virion - isolation & purification; Virus-like particle; VLP
• ISSN: 0304-4165; 0006-3002; 1872-8006
• DOI: 10.1016/0304-4165(95)00184-0

Three capsid proteins of SV40 (VP1, VP2, and VP3) were expressed in insect cells using recombinant baculoviruses. When the VP1 capsid protein was expressed alone or co-expressed with VP2 and VP3, virus-like particles (VLP) were produced. In the latter case, the minor capsid proteins, VP2 and VP3, were incorporated into the VLP. VLPs with and without VP2 and VP3, and the wild type SV40 virions were indistinguishable under electron microscope. The sedimentation coefficient, s 20, w, obtained for the VLP consisting of VP1 alone (VP1-VLP) was 170 S, and that for the VLP consisting of all of the capsid proteins (VP1/2/3-VLP) was 174 S. Treatment of the VP1-VLP with a calcium ion chelating agent and a reducing agent caused dissociation of the VP1-VLP. The dissociated and purified VP1 proteins were identified as pentamers of VP1 based on the molecular weight determination by sedimentation equilibrium. The pentamers were shown to possess the ability to re-assemble into VLP which had the s 20, w of 141S. The results are discussed in relation to the morphogenesis of SV40.