|
|
||||||||
Animal Virus Research Institute, Pirbright, Surrey
Methods for the purification of African swine fever virus (ASFV) and its dissection into two fractions are described. The difficulties which have been encountered previously in attempts to purify the virus, namely contamination with large amounts of cellular constituents and aggregation of the virus particles, have been overcome by treatment with Tween 80 and by the use of 1M-NaCl in the sucrose gradients. Five major polypeptides, mol. wt. 103 x 125 (VP1), 76 (VP2), 50 (VP3), 44 (VP4) and 39 (VP5) were found in the purified particles. The virus was dissected by treatment with Nonidet NP 40 into (a) a fraction which had the appearance of an empty capsid shell and contained the polypeptides VP2 and VP3 and (b) a structure containing VP1 and VP4. The location of VP5 was not ascertained.
Received 1 March 1976;
accepted 29 April 1976.
This article has been cited by other articles:
![]() |
C. Cobbold, M. Windsor, J. Parsley, B. Baldwin, and T. Wileman Reduced redox potential of the cytosol is important for African swine fever virus capsid assembly and maturation J. Gen. Virol., January 1, 2007; 88(1): 77 - 85. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Rouiller, S. M. Brookes, A. D. Hyatt, M. Windsor, and T. Wileman African Swine Fever Virus Is Wrapped by the Endoplasmic Reticulum J. Virol., March 1, 1998; 72(3): 2373 - 2387. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |