J
Juergen Kast
Researcher at University of British Columbia
Publications - 34
Citations - 2481
Juergen Kast is an academic researcher from University of British Columbia. The author has contributed to research in topics: Mass spectrometry & Proteomics. The author has an hindex of 19, co-authored 34 publications receiving 2305 citations.
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Journal ArticleDOI
CIP2A Inhibits PP2A in Human Malignancies
Melissa R. Junttila,Pietri Puustinen,Minna Niemelä,Minna Niemelä,Raija Ahola,Hugh Arnold,Trine Bøttzauw,Risto Ala-aho,Christina Nielsen,Johanna Ivaska,Johanna Ivaska,Yoichi Taya,Shi-Long Lu,Shujun Lin,Edward K. L. Chan,Xiao-Jing Wang,Reidar Grénman,Reidar Grénman,Juergen Kast,Tuula Kallunki,Rosalie C. Sears,Veli-Matti Kähäri,Veli-Matti Kähäri,Jukka Westermarck,Jukka Westermarck,Jukka Westermarck +25 more
TL;DR: The data show that CIP2A is a human oncoprotein that inhibits PP2A and stabilizes c-Myc in human malignancies and promotes anchorage-independent cell growth and in vivo tumor formation.
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Utility of formaldehyde cross-linking and mass spectrometry in the study of protein-protein interactions.
TL;DR: Key advantages and limitations to the use of formaldehyde over other cross-linkers and technologies currently used to study protein-protein interactions are highlighted, and formaldehyde-based experimental approaches that are proving very promising in their ability to accurately and efficiently identify novel protein- protein and multiprotein interaction complexes are presented.
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Identification of protein-protein interactions using in vivo cross-linking and mass spectrometry.
TL;DR: A novel method for identifying transient protein‐protein interactions using in vivo cross‐linking and MS‐based protein identification is described and the RasGAP‐related protein IQGAP1 is identified to be a novel interaction partner of M‐RasQ71L.
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Optimization of Formaldehyde Cross-Linking for Protein Interaction Analysis of Non-Tagged Integrin β1
TL;DR: Formaldehyde cross-linked complexes, precipitated from Jurkat cells or human platelets and analyzed by mass spectrometry, were found to be composed of integrin β 1, α4 and α6 or β1, α6, α2, and α5, respectively.
Journal ArticleDOI
Deconstruction of the SS18-SSX Fusion Oncoprotein Complex: Insights into Disease Etiology and Therapeutics
Le Su,Arthur V. Sampaio,Kevin B. Jones,Kevin B. Jones,Marina Pacheco,Angela Goytain,Shujun Lin,Neal M. Poulin,Lin Yi,Fabio M.V. Rossi,Juergen Kast,Mario R. Capecchi,T. Michael Underhill,Torsten O. Nielsen +13 more
TL;DR: A fundamental role is defined for aberrant ATF2 transcriptional dysregulation in the etiology of synovial sarcoma through its role as a bridge between activating transcription factor 2 (ATF2) and transducin-like enhancer of split 1 (TLE1).