ChemInform Abstract: Backbone Amide Linker Strategy: Protocols for the Synthesis of C-Terminal Peptide Aldehydes

ChemInform ◽  
2015 ◽  
Vol 46 (20) ◽  
pp. no-no
Author(s):  
Pernille Tofteng Shelton ◽  
Knud J. Jensen
2000 ◽  
Vol 41 (32) ◽  
pp. 6131-6135 ◽  
Author(s):  
Fanny Guillaumie ◽  
Joseph C Kappel ◽  
Nicholas M Kelly ◽  
George Barany ◽  
Knud J Jensen

Author(s):  
Fanny Guillaumie ◽  
Nicholas M. Kelly ◽  
Joseph C. Kappel ◽  
George Barany ◽  
Knud J. Jensen

ChemInform ◽  
2006 ◽  
Vol 37 (9) ◽  
Author(s):  
Jordi Alsina ◽  
Steven A. Kates ◽  
George Barany ◽  
Fernando Albericio

Chemosensors ◽  
2021 ◽  
Vol 9 (12) ◽  
pp. 359
Author(s):  
David Milićević ◽  
Jan Hlaváč

A new approach to on-resin detection of three model proteases (trypsin, chymotrypsin, and thrombin) has been developed, while at the same time already described methodology for simultaneous detection of two enzymes (trypsin and chymotrypsin) has been additionally generalized. Appropriate immobilized substrates, comprising specifically cleavable peptide sequences capped with fluorescent dyes, have been synthesized on Rink Amide PEGA resin or Amino PEGA resin modified with backbone amide linker (BAL). Resulting solid support-bound probes were then dispersed into Tris-HCl buffer solution (pH = 8.0) and subjected to enzymatic cleavage. Liberated fluorophores have been tracked by fluorescence measuring. The competitive activities of studied proteases towards the thrombin probe have been efficiently limited and controlled by employing a Bowman-Birk inhibitor into a system.


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