A photochemical transformation of cyclic peptides leading to formation of selenolanthionine bridges

2020 ◽  
Vol 44 (27) ◽  
pp. 11433-11436
Author(s):  
Mateusz Waliczek ◽  
Özge Pehlivan ◽  
Piotr Stefanowicz

Peptides with diselenide bridge under UV irradiation eliminate one selenium atom forming selenoether bond with good yield.

2018 ◽  
Vol 20 (6) ◽  
pp. 3895-3902 ◽  
Author(s):  
Dinesh Mishra ◽  
Sisi Wang ◽  
Serge Michel ◽  
Goutam Palui ◽  
Naiqian Zhan ◽  
...  

We have combined optical absorption with the Ellman's test to identify the parameters that affect the transformation of the 5-membered dithiolanes to thiols in lipoic acid (LA) and its derivatives during UV-irradiation.


2014 ◽  
Vol 1053 ◽  
pp. 317-322
Author(s):  
Ning Ning Lv ◽  
Yan Zhang

2-Indolylfulgimide was synthesized to examine the practical dyeing feasibilities and behaviors. A one-pot efficient process was discovered with good yield (52%). The color changing properties of fulgimide in solvents and on wool fibers were investigated. With UV irradiation, fulgimide showed color variation from light yellow to light red. The same color changing behavior appeared in the wool fiber which was dyed with 2-indolylfulgimide through a normal acid dye dyeing process.


Planta Medica ◽  
2011 ◽  
Vol 77 (12) ◽  
Author(s):  
D Craik ◽  
A Poth ◽  
M Colgrave ◽  
M Akcan ◽  
B Oku ◽  
...  

Planta Medica ◽  
2014 ◽  
Vol 80 (16) ◽  
Author(s):  
F El Maddah ◽  
M Nazir ◽  
S Kehraus ◽  
GM König
Keyword(s):  

2001 ◽  
Vol 73 (2) ◽  
pp. 147 ◽  
Author(s):  
Yukihito Kabuyama ◽  
Miwako K. Homma ◽  
Masayuki Sekimata ◽  
Yoshimi Homma

2020 ◽  
Author(s):  
Salvador Guardiola ◽  
Monica Varese ◽  
Xavier Roig ◽  
Jesús Garcia ◽  
Ernest Giralt

<p>NOTE: This preprint has been retracted by consensus from all authors. See the retraction notice in place above; the original text can be found under "Version 1", accessible from the version selector above.</p><p><br></p><p>------------------------------------------------------------------------</p><p><br></p><p>Peptides, together with antibodies, are among the most potent biochemical tools to modulate challenging protein-protein interactions. However, current structure-based methods are largely limited to natural peptides and are not suitable for designing target-specific binders with improved pharmaceutical properties, such as macrocyclic peptides. Here we report a general framework that leverages the computational power of Rosetta for large-scale backbone sampling and energy scoring, followed by side-chain composition, to design heterochiral cyclic peptides that bind to a protein surface of interest. To showcase the applicability of our approach, we identified two peptides (PD-<i>i</i>3 and PD-<i>i</i>6) that target PD-1, a key immune checkpoint, and work as protein ligand decoys. A comprehensive biophysical evaluation confirmed their binding mechanism to PD-1 and their inhibitory effect on the PD-1/PD-L1 interaction. Finally, elucidation of their solution structures by NMR served as validation of our <i>de novo </i>design approach. We anticipate that our results will provide a general framework for designing target-specific drug-like peptides.<i></i></p>


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