Structural Analysis of Guanylyl Cyclase-Activating Protein-2 (GCAP-2) Homodimer by Stable Isotope-Labeling, Chemical Cross-Linking, and Mass Spectrometry

2013 ◽  
Vol 24 (12) ◽  
pp. 1969-1979 ◽  
Author(s):  
Jens Pettelkau ◽  
Iris Thondorf ◽  
Stephan Theisgen ◽  
Hauke Lilie ◽  
Thomas Schröder ◽  
...  
2002 ◽  
Vol 277 (48) ◽  
pp. 46487-46492 ◽  
Author(s):  
Thomas Taverner ◽  
Nathan E. Hall ◽  
Richard A. J. O'Hair ◽  
Richard J. Simpson

2018 ◽  
Vol 90 (3) ◽  
pp. 1852-1860 ◽  
Author(s):  
Maud Heuillet ◽  
Floriant Bellvert ◽  
Edern Cahoreau ◽  
Fabien Letisse ◽  
Pierre Millard ◽  
...  

2012 ◽  
Vol 18 (8) ◽  
pp. 2342-2348 ◽  
Author(s):  
Helge B. Bode ◽  
Daniela Reimer ◽  
Sebastian W. Fuchs ◽  
Ferdinand Kirchner ◽  
Christina Dauth ◽  
...  

Synthesis ◽  
2020 ◽  
Vol 52 (14) ◽  
pp. 2106-2110
Author(s):  
Nicolas Philippe ◽  
Serge Pérard ◽  
Franck Le Strat ◽  
Jörg Blankenstein ◽  
Sébastien Roy

With a view to make conveniently labeled mass spectrometry standards available, a set of deuterated sphingomyelins were prepared by a new expedient, flexible, robust, scalable, and high-yielding synthetic scheme starting from 2-azido-3-O-benzoylsphingosine as the key intermediate. Unlike previously published procedures, this work emphasizes the benefit arising from the choice of the azido function as a masking group for the reactive primary amine during the troublesome, though crucial, phosphorylation step.


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