Felix Wieland
- 1968-1973 Study of chemistry at the University
of Munich
- 1974-1978 Diploma and PhD Student at the
Max Planck-Institut für Biochemie, Munich
- 1976-1978 Research assistant at the Max-Planck-Institut
für Biochemie, Munich
- 1984 Habilitation in Biochemistry
- 1984-1986 Senior research assistant at
the University of Regensburg
- 1986-1988 Visiting scientist at the Department
of
- Biochemistry, Stanford University, USA
- 1988-1996 C4 Professor at Heidelberg University,
Faculties of Medicine and Biology, Chair of Biochemistry Institute
I
- 1997 Chair of Biochemie-Zentrum Heidelberg
(BZH)
- Contact:
-
- Felix Wieland, Universität Heidelberg,
Biochemie-Zentrum (BZH),
- Im Neuenheimer Feld 328
- D-69120 Heidelberg,
- Tel. +49-6221-544150
- Fax: +49-6221-544366,
- e-mail: felix.wieland@urz.uni-heidelberg.de
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Biogenesis Of Transport Vesicles
Current Research
The last step in the biosynthesis of membrane
proteins and secreted proteins is vesicular transport to their
destinations. Likewise, many membrane lipids are transported
in vesicles. My lab focuses on the characterization of COPI-coated
vesicles that are involved in anterograde and retrograde protein
transport in the early secretory pathway of eukaryotic cells.
In the past we have characterized a variety of protein components
of the machinery used for the generation of COPI-coated vesicles.
In addition, we have determined the rate at which these vesicles
travel through the cell. Recently we have characterized a coat-receptor
protein in the membrane of COPI-coated vesicles and shown that
coat recruitment involves a bivalent interaction of coatomer
with the donor membrane. These minimal requirements for the formation
of a COPI-vesicle we have confirmed in a chemically defined in
vitro system. In addition we have observed a segregation of membrane
lipids from COPI-vesicles.
Projects for a doctoral thesis
For the next couple of years our research
will focus on the molecular mechanisms of COPI-vesicle generation.
We will analyse both the mechanisms that allow cargo to be included
and resident Golgi proteins to be excluded from a forming vesicle,
and the sorting of membrane Lipids. The methods applied will
include in vivo and in vitro transport assays, protein chemistry,
molecular biology, ultra structural analysis of cells and isolated
organelles, as well as lipid biochemistry.
Our long term goal is to elucidate at a
molecular level the functional organization of the endomembrane
system with respect to biosynthesis and specific transport of
proteins and lipids.

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