Evelyne Kretzschmar
Yale University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Evelyne Kretzschmar.
Journal of General Virology | 1995
J. Hausmann; Evelyne Kretzschmar; Wolfgang Garten; Hans-Dieter Klenk
The neuraminidase (NA) gene of influenza virus A/FPV/Rostock/34 virus (H7N1) was cloned and expressed in Sf9 cells using a baculovirus vector. The expression product had the expected molecular mass and showed neuraminidase activity. NA expressed in Sf9 cells also showed haemagglutinating activity as indicated by its ability to induce haemadsorption of chicken red blood cells. Haemadsorption depended on the presence of neuraminic acid on the erythrocytes, but was not blocked by 2-deoxy-2,3-dehydro-N-acetylneuraminic acid, a specific inhibitor of the enzymatic activity. These observations suggest that the N1 neuraminidase has two distinct reactive sites: a catalytic site and a receptor binding site. This concept was confirmed by site-directed mutagenesis which showed that the haemadsorbing activity of FPV NA was abolished when amino acids located on two surface loops at the putative binding site were exchanged. Substitutions on either of the two loops were sufficient for this effect. The mutated NAs retained full neuraminidase activity. In contrast, a mutated NA lacking neuraminidase activity still had haemadsorbing activity.
Journal of General Virology | 1997
J. Hausmann; Evelyne Kretzschmar; Wolfgang Garten; Hans-Dieter Klenk
Intracellular transport, glycosylation, tetramerization and enzymatic activity of the neuraminidase (NA) of fowl plague virus (FPV) were analysed in vertebrate cells after expression from a vaccinia virus vector. Tetramerization occurred with a half-time of 15 min, whereas passage through the medial Golgi apparatus and transport to the plasma membrane occurred with half-times of 2 and 3 h, respectively, suggesting a step in NA maturation beyond tetramerization that limits the rate of transport to the medial Golgi. NA transport rates were about fourfold slower than those of haemagglutinin (HA). Slow transport and processing of FPV NA was not altered by coexpression of FPV HA, nor was the transport rate of HA influenced by NA. The slow transport kinetics of NA were also observed in FPV-infected CV-1 cells. As deduced from the coding sequence, FPV NA has the shortest stalk of all naturally occurring NAs described to date and contains only three potential N-glycosylation sites, which are all located in the globular head domain. Elimination of each of the three N-glycosylation sites revealed that the two oligosaccharides at positions 124 and 66 are of the complex type, whereas the one at Asn-213 remains in mannose-rich form. The glycosylation mutants showed also that oligosaccharides at positions 124 and 213 of FPV NA modulate enzymatic activity. Transport of NA is not influenced by single elimination of any of the three oligosaccharide attachment sites. Mutational analysis of the three Cys residues not involved in intrachain disulfide pairing revealed that Cys-49 in the stalk of the NA molecule is responsible for the formation of disulfide-linked dimers. Analysis of cysteine mutants of FPV NA also demonstrated that disulfide-linked dimers are not absolutely necessary for the formation of enzymatically active tetramers but may stabilize the quaternary structure of NA.
Journal of General Virology | 1992
Evelyne Kretzschmar; Michael Veit; Sabine Brunschön; Kazumichi Kuroda; Hans-Dieter Klenk
In the present study we have investigated the role of the hydrophobic domains of the fowl plague virus (FPV) haemagglutinin (HA) on its intracellular transport and maturation in insect cells. To this end processing of full-length HA (A+) has been compared to that of two truncated forms lacking either the cytoplasmic domain and the transmembrane domain (A-) or lacking the entire HA2 subunit, i.e. the transmembrane domain and the fusion peptide (HA2-). All glycosylation sites present on A- and HA2- were glycosylated, indicating that both truncated forms were completely translocated in the endoplasmic reticulum. Unlike A+, A- and HA2- did not form trimers as indicated by cross-linking, gradient centrifugation and studies employing conformation-specific antibodies. Whereas HA2- was efficiently secreted, A- was retained in the cells in an apparently membrane-bound form. The data show that the carboxy-terminal transmembrane region is essential for the formation and stability of the trimers of the FPV HA. These observations also indicate that, under certain conditions, the fusion peptide of the FPV HA can serve as a membrane anchor.
Proceedings of the National Academy of Sciences of the United States of America | 1996
Matthias J. Schnell; Linda Buonocore; Evelyne Kretzschmar; E Johnson; John K. Rose
Journal of Virology | 1998
Anjeanette Roberts; Evelyne Kretzschmar; Archibald S. Perkins; John P. Forman; Ryan Price; Linda Buonocore; Yoshihiro Kawaoka; John K. Rose
Journal of Virology | 1997
Evelyne Kretzschmar; Linda Buonocore; Matthias J. Schnell; John K. Rose
Journal of Virology | 1991
Michael Veit; Evelyne Kretzschmar; Kazumichi Kuroda; Wolfgang Garten; M. F. G. Schmidt; Hans-Dieter Klenk; R. Rott
Virology | 1996
Evelyne Kretzschmar; Matthew Bui; John K. Rose
Virology | 1996
Evelyne Kretzschmar; Richard W. Peluso; Matthias J. Schnell; Michael A. Whitt; John K. Rose
Glycobiology | 1996
Ralf Wagner; Steffen Liedtke; Evelyne Kretzschmar; Hildegard Geyer; Rudolf Geyer; Hans-Dieter Klenk