THE HANDICRAFT OF CELLULAR TRANSPORT COMPLEXES
A protein complex, which is an important link in a cellular transport chain, also initiates the
assembly of the next link in the chain. This newly-won insight will now allow a better
understanding of a transport process that plays a crucial role in numerous cellular processes
including virus infections, cell division and signal transmission. The additional function of the
ESCRT-II transport complex was discovered during the course of a research project funded by
the Austrian Science Fund FWF and recently reported in "The EMBO Journal".
(firmenpresse) - Virus infections, cell division and signal transmission have something in common: they
make use of a "protein machine" that actually controls a cell disposal process. The
assembly of this molecular "machine" is highly controlled and is mainly influenced by five
particular protein complexes. The protein complexes in question are referred to as ESCRTs
(endosomal-sorting complex required for transport). A team from Innsbruck Medical
University and Cornell University in the USA has now discovered a surprising function of
one of the ESCRT complexes (No II): ESCRT-II also initiates the assembly of ESCRT-III,
the central complex in the transport chain.
MOLECULAR TRAFFIC CONTROL
All ESCRTs share the function of loading the cellular transport vesicles (MVB - multi
vesicular bodies) with cell surface components that have become "unwanted". For this
purpose, the ESCRTs are generated only temporarily. Dr. David Teis from the Division of
Cell Biology at Innsbruck Medical Hospital explains the new function of one of the ESCRTs
discovered by his team as follows: "A part of ESCRT-II, known as Vps25, triggers a kind of
chain reaction, which initially gives rise to a structural change in another protein called
Vps20. Vps20 is more or less activated by the structural change and other proteins -
SnF7s - can then group around Vps20. Subsequently, the rest of the ESCRT-III forms
around this starting point. In this way, ESCRT-II initiates the assembly of ESCRT-III."
To be more precise, approximately 10 - 20 Snf7 proteins must assemble in a defined ring-
like form so that the other ESCRT-III components can be added as required. It is precisely
this ring-like grouping of the Snf7 proteins that is influenced by the Vps25. The team
working with Dr. Teis was able to discover this through experiments involving the clever
modification of ESCRT-IIs: instead of the usual two Vps25s, only one was used for
ESCRT-II. Dr. Teis explains: "This enabled us to show that, despite the reduced number of
Vps25s in the ESCRT-II, the Snf7s still grouped together. However, the molecules that
assembled in this way were not able to fulfill the biological function of ESCRT-III."
NO "O" WITHOUT "Y"
Based on the known fact that the two Vps25 proteins of the ESCRT-II form a Y-shaped
structure, Dr. Teis made the following deduction from this finding: the two arms of the Y
formed by the Vps25 together enable the suitable ring-shaped arrangement of the Snf7
molecules. While one "arm" is sufficient to group the Snf7s, two Snf7s must be deposited -
one on each arm - for the spatial structure to accommodate the further assembly of the
ESCRT-III.
This ring structure then acts as a kind of master copy for the MBV transport vesicles. This
assumption was confirmed in a further experiment which Dr. Teis carried out with his co-
operation partner Professor Scott Emr from Cornell University in the USA. For this
experiment, more Snf7 molecules than usual were formed in cells with an altered molecular
composition. The result? The vesicles that formed in these cells were significantly larger -
providing a clear indication of the role of the Snf7 protein as a master copy.
In summary, these results, stemming from an FWF project, not only reveal the extent to
which this cellular disposal mechanism is finely tuned, but also demonstrate its hitherto
unknown capacity for molecular self-assembly.
Image and text will be available from Tuesday, 25th May 2010, 9.00 a.m. CET onwards:
http://www.fwf.ac.at/en/public_relations/press/pv201005-en.html
Original publication: ESCRT-II coordinates the assembly of ESCRT-III filaments for cargo
sorting and multivesicular body vesicle formation, D. Teis, S. Saksena, B. Judson and S. D.
Emr, The EMBO Journal (2010) 29, 871 - 883 doi:10.1038/emboj.2009.408
Scientific contact:
Dr. David Teis
Innsbruck Medical University
Division of Cell Biology
Fritz-Pregl Str. 3
6020 Innsbruck
T +43 / 512 / 9003 - 70175
E david.teis(at)i-med.ac.at
The Austrian Research Foundation FWF:
Mag. Stefan Bernhardt
Haus der Forschung
Sensengasse 1
1090 Vienna
T +43 / 1 / 505 67 40 - 8111
E stefan.bernhardt(at)fwf.ac.at
W http://www.fwf.ac.at
Publication and distribution:
PR&D - Public Relations für Forschung & Bildung
Campus Vienna Biocenter 2
1030 Vienna
T +43 / 1 / 505 70 44
E contact(at)prd.at
W http://www.prd.at
Vienna, 25th May 2010
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