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John J.M. Bergeron

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John J. M. Bergeron, D. Phil.

Professor, Department of Medicine
Co-Director of the Laboratory of Systems Medicine and Cell Biology
687 Pine Avenue, Room M3.20B, Montreal, QC H3A 1A1

Tel: 514-934-1934 ext. 35702

john.bergeron [at] mcgill.ca

Biographical Sketch

Dr. Bergeron has studied polypeptide hormone and growth factor receptor activation and signaling, and especially the spatial and temporal regulation of hormone and growth factor action in target organs. He has also studied extensively the fundamental mechanisms for secretion of N linked glycoproteins from all eukaryotic cells through mechanistic studies on the protein calnexin which he uncovered. Dr. Bergeron is an expert on high throughput approaches and especially organellar proteomics and is a co-founder with Tom Hudson of the ÎÛÎÛ²ÝÝ®ÊÓƵ University/Genome Quebec Innovation Centre and co-founder of Caprion Proteomics. Dr. Bergeron is a Fellow of the Royal Society of Canada and McLaughlin gold medal awardee of the Royal Society of Canada. Dr. Bergeron was also honored with the Human Proteome Organization Discovery Award.

Keywords

Human and animal organs, Organelles, Cell Map, Protein Microscope, Cell based assays, Cell free assays

Research or Clinical Activities

Organs including those of the endocrine system have evolved to regulate homeostasis, and insults either through the environment or the genetic complement of the family will lead to disease. My lab studies quantitatively the proteins in human and animal organs to uncover their functions in health and disease. The strategy is based on a technology we have named as the Protein Microscope. By the assiduous processing of samples from human and model organisms, we have characterized proteins within organelles (small intracellular compartments responsible for cell homeostasis) isolated from organs (liver, pancreas, islets of Langerhans, testis, epididymis) linked to health and disease. This has already enabled the assignment of proteins to mechanisms fundamental to homeostasis and proteins linked to organelles in organ samples from humans with disease. Our ultimate goal is the assignment of all predicted 20,000 human protein coding genes to the cognate organelles of the >250 different cell types making up the organs of the human to define a cell map and thereby uncover the mechanistic basis of health and disease.

Selected Recent Publications

Quantitative proteomics analysis of the secretory pathway. Gilchrist A, Au CE, Hiding J, Bell AW, Fernandez-Rodriguez J, Lesimple S, Nagaya H, Roy L, Gosline SJ, Hallett M, Paiement J, Kearney RE, Nilsson T, Bergeron JJ. Cell. 2006 Dec 15;127(6):1265-81.

A HUPO test sample study reveals common problems in mass spectrometry-based proteomics. Bell AW, Deutsch EW, Au CE, Kearney RE, Beavis R, Sechi S, Nilsson T, Bergeron JJ; HUPO Test Sample Working Group. Nat Methods. 2009 Jun;6(6):423-30. doi: 10.1038/nmeth.1333.

Cell biology of the endoplasmic reticulum and the Golgi apparatus through proteomics. Smirle J, Au CE, Jain M, Dejgaard K, Nilsson T, Bergeron J. Cold Spring Harb Perspect Biol. 2013 Jan 1;5(1):a015073. doi: 10.1101/cshperspect.a015073. PMID: 23284051

Mass spectrometry in high-throughput proteomics: ready for the big time. Nilsson T, Mann M, Aebersold R, Yates JR 3rd, Bairoch A, Bergeron JJ. Nat Methods. 2010 Sep;7(9):681-5. doi: 10.1038/nmeth0910-681. PMID: 20805795

Organellar proteomics to create the cell map. Au CE, Bell AW, Gilchrist A, Hiding J, Nilsson T, Bergeron JJ. Curr Opin Cell Biol. 2007 Aug;19(4):376-85.

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