|
|
||||||||
Animal: DNA Viruses |
Department of Virology, SMI/Karolinska Institute, 171 82 Solna, Sweden 1
Department of Immunology, Microbiology, Pathology and Infectious Disease, Karolinska Institute, Box 12 773, 112 96 Stockholm, Sweden 2
Author for correspondence: Lennart Svensson.Fax +46 8 301635. e-mail Lensve{at}mbox.ki.se
The membrane-impermeable thiol blocker 5'5-dithiobis 2- nitrobenzoic acid (DTNB) blocked infectivity of human cytomegalovirus (CMV) although the virus still bound to cells. DTNB-treated CMV regained 65% of its infectivity after incubation with the disulfide bond-reducing agent dithiothreitol. These observations suggest that free thiol groups on CMV are required for infectivity and may participate in disulfide bond formation during virus entry.
This article has been cited by other articles:
![]() |
T. R. Jones, S.-W. Lee, S. V. Johann, V. Razinkov, R. J. Visalli, B. Feld, J. D. Bloom, and J. O'Connell Specific Inhibition of Human Cytomegalovirus Glycoprotein B-Mediated Fusion by a Novel Thiourea Small Molecule J. Virol., February 1, 2004; 78(3): 1289 - 1300. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Wieringa, A. A. F. de Vries, and P. J. M. Rottier Formation of Disulfide-Linked Complexes between the Three Minor Envelope Glycoproteins (GP2b, GP3, and GP4) of Equine Arteritis Virus J. Virol., June 1, 2003; 77(11): 6216 - 6226. [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 | |