Following protein biogenesis, proteins are trafficked to different cellular compartments within the cell from either the endoplamsic reticulum, or (mostly) the golgi apparatus.
This assessed presentation was delivered to a group of fellow students during the stage 2 (in April 2013) of my studies.
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''VESICLE TETHERING'' Presentation By KATE, Wisdom Deebeke
1. Presentation
By
Kate, Wisdom Deebeke
on
Vesicle Tethering
Objective
To understand the mechanism of Vesicle
Tethering.
2. Vesicle Tethering, what is it?
Formation of physical links between v- and t-SNARES
Formed before TRANS SNARE complex formation
Aimed at promoting specificity between two membranes
Growing number of factors involved now identified, all
recruited by Rab GTPase.
3. Tethering factors
Two broad classes of molecules identified:
a) Long coiled-coil proteins
Form homodimeric coiled-coils
E.g. Uso1p (in yeast) and P115 (in mammals)
Essential for tethering ER-derived vesicles
b) Multisubunit tethering complexes
7 large conserved complexes proposed
Initially identified in yeasts
E.g. include exocyst, COG complex, TRAPP, etc.
TRAPP-1 involved in ER-Golgi anterograde transport
Image from: Whyte, J. R. C. and S. Munro (2002). "Vesicle tethering complexes in membrane traffic." Journal of Cell
Science 115(13): 2627-2637.
4. Summary
Vesicle tethering important for specific localisation of
transport vesicles on membranes
Many factors involved have been identified and
characterised
Rab GTPase plays important role in Tethering factor
recruitment
References:
1. Whyte, J. R. C. and S. Munro (2002). "Vesicle tethering complexes in
membrane traffic." Journal of Cell Science 115(13): 2627-2637
2. Olkkonen, V. M. and E. Ikonen (2006). "When intracellular logistics fails -
genetic defects in membrane trafficking." Journal of Cell Science 119(24):
5031-5045.