Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation
DMM Jaradat - Amino acids, 2018 - Springer
A historical overview of peptide chemistry from T. Curtius to E. Fischer to M. Bergmann and
L. Zervas is first presented. Next, the fundamentals of peptide synthesis with a focus on solid …
L. Zervas is first presented. Next, the fundamentals of peptide synthesis with a focus on solid …
Ligation technologies for the synthesis of cyclic peptides
Cyclic peptides have been attracting a lot of attention in recent decades, especially in the
area of drug discovery, as more and more naturally occurring cyclic peptides with diverse …
area of drug discovery, as more and more naturally occurring cyclic peptides with diverse …
Chemical protein synthesis: advances, challenges, and outlooks
Contemporary chemical protein synthesis has been dramatically advanced over the past few
decades, which has enabled chemists to reach the landscape of synthetic …
decades, which has enabled chemists to reach the landscape of synthetic …
Serine/threonine ligation: origin, mechanistic aspects, and applications
Conspectus Synthetic proteins are expected to go beyond the boundary of recombinant
DNA expression systems by being flexibly installed with site-specific natural or unnatural …
DNA expression systems by being flexibly installed with site-specific natural or unnatural …
Oxidation and phenolysis of peptide/protein C-terminal hydrazides afford salicylaldehyde ester surrogates for chemical protein synthesis
S Lin, Z Mo, P Wang, C He - Journal of the American Chemical …, 2023 - ACS Publications
With the growing popularity of serine/threonine ligation (STL) and cysteine/penicillamine
ligation (CPL) in chemical protein synthesis, facile and general approaches for the …
ligation (CPL) in chemical protein synthesis, facile and general approaches for the …
Discovery of Biologically Optimized Polymyxin Derivatives Facilitated by Peptide Scanning and In Situ Screening Chemistry
R Kaguchi, A Katsuyama, T Sato… - Journal of the …, 2023 - ACS Publications
Peptides can be converted to highly active compounds by introducing appropriate
substituents on the suitable amino acid residue. Although modifiable residues in peptides …
substituents on the suitable amino acid residue. Although modifiable residues in peptides …
Enabling chemical protein (semi) synthesis via reducible solubilizing tags (RSTs)
Chemical synthesis of proteins with poor solubility presents a challenging task. The existing
solubilizing tag strategies are not suitable for the expressed protein segment. To address …
solubilizing tag strategies are not suitable for the expressed protein segment. To address …
Robust Chemical Synthesis of “Difficult Peptides” via 2-Hydroxyphenol-pseudoproline (ψ2-hydroxyphenolpro) Modifications
X Wang, K Jin - The Journal of organic chemistry, 2024 - ACS Publications
The challenging preparation of “difficult peptides” has always hindered the development of
peptide-active pharmaceutical ingredients. Pseudoproline (ψpro) building blocks have been …
peptide-active pharmaceutical ingredients. Pseudoproline (ψpro) building blocks have been …
O-to-O acyl transfer for epimerization-free peptide C-terminal salicylaldehyde ester synthesis
W Xia, BW Li, Z Zhong, J Liu, H Liu, ZX Yu, X Li - Nature Synthesis, 2024 - nature.com
Peptide salicylaldehyde esters are the requisite coupling partner in Ser/Thr ligation
reactions towards chemical protein synthesis. In general, it would be cost-effective and …
reactions towards chemical protein synthesis. In general, it would be cost-effective and …
Recent advances in protein modifications techniques for the targeting N‐terminal cysteine
N‐terminal modifications of proteins have garnered the attention of chemical biologists
because of their critical roles in numerous cellular processes, including protein …
because of their critical roles in numerous cellular processes, including protein …