Lee Sweetlove Department of Plant Sciences, University of Oxford, UK
1 protocol

J. Andrew Smith Department of Plant Sciences, University of Oxford, UK
1 protocol

Charles Baxter Syngenta, Jealott's Hill International Research Centre, UK
1 protocol

Benjamin Thomas Central Proteomics Facility, Sir William Dunn Pathology School, University of Oxford, UK
1 protocol

Christopher J. Snowden
  • Department of Plant Sciences, University of Oxford, UK
Research focus
  • Plant science
  • 1 Author merit


Ph.D. in Biological Sciences, from Faculty of Biological Sciences, University of Leeds, 2007

Current position

Senior Biology Technician, Rugby School


  1. Snowden, C. J., Thomas, B., Baxter, C. J., Smith, J. A. and Sweetlove, L. J. (2015). A tonoplast Glu/Asp/GABA exchanger that affects tomato fruit amino acid composition. Plant J 81(5): 651-660.
  2. Marshall, R. S., Jolliffe, N. A., Ceriotti, A., Snowden, C. J., Lord, J. M., Frigerio, L. and Roberts, L. M. (2008). The role of CDC48 in the retro-translocation of non-ubiquitinated toxin substrates in plant cells. J Biol Chem 283(23): 15869-15877.
  3. Snowden, C. J., Leborgne-Castel, N., Wootton, L. J., Hadlington, J. L. and Denecke, J. (2007). In vivo analysis of the lumenal binding protein (BiP) reveals multiple functions of its ATPase domain. Plant J 52(6): 987-1000.
  4. Pimpl, P., Taylor, J. P., Snowden, C., Hillmer, S., Robinson, D. G. and Denecke, J. (2006). Golgi-mediated vacuolar sorting of the endoplasmic reticulum chaperone BiP may play an active role in quality control within the secretory pathway. Plant Cell 18(1): 198-211.
  5. daSilva, L. L., Taylor, J. P., Hadlington, J. L., Hanton, S. L., Snowden, C. J., Fox, S. J., Foresti, O., Brandizzi, F. and Denecke, J. (2005). Receptor salvage from the prevacuolar compartment is essential for efficient vacuolar protein targeting. Plant Cell 17(1): 132-148.
1 Protocol published
Isolation of Tonoplast Vesicles from Tomato Fruit Pericarp
This protocol describes the isolation of tonoplast vesicles from tomato fruit. The vesicles isolated using this procedure are of sufficiently high purity for downstream proteomic analysis whilst remaining transport competent for functional assays. ...
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