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Updated: Sep 1, 2025

Methods for Evaluating the Role of c-Fos and Dusp1 in Oncogene Dependence
Published on: January 7, 2019
Synthesis of the l- and d-SH2 domain of the leukaemia oncogene Bcr-Abl
Nina Schmidt1, Frank Abendroth2, Olalla Vázquez2,3
1Institute of Physiological Chemistry, University of Marburg 35032 Marburg Germany oliver.hantschel@uni-marburg.de.
Abstract:
The d- and l-versions of the Bcr-Abl SH2 domain (12.7 kDa) were synthesized. Key optimizations included pseudoproline incorporation, N-terminal hydrophilic tail addition and mild N-acetoxy succinimide acetylation. Their folding and activity are as for the recombinant protein. Our results will enable engineering of mirror-image monobody antagonists of the central oncoprotein Bcr-Abl.
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