<i>N,S</i>
            ‐ and
            <i>N,Se</i>
            ‐Acyl Transfer Devices in Protein Synthesis

Diemer, Vincent; Bouchenna, Jennifer; Kerdraon, Florent; Agouridas, Vangelis; Melnyk, Oleg

doi:10.1002/9783527823567.ch3

Cited by 5 publications

(1 citation statement)

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“…To sum up at this stage, the SEA off amide group discussed above enriches the growing family of latent thioester systems, which include peptide hydrazides 48 , 49 and some N , S -acyl shift systems 50 , 51 such as protected cysteinyl prolyl esters 52 or photocaged SEAlide. 53 However, at this stage, the SEA off group appears as a single shot rifle enabling no more than three peptide segments to be assembled in one-pot (see Figure 2 ).…”

Section: Carboxamides As Redox-controlled Latent Thioestersmentioning

confidence: 99%

Redox-Controlled Chemical Protein Synthesis: Sundry Shades of Latency

et al. 2022

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Conspectus The last two decades have witnessed the rise in power of chemical protein synthesis to the point where it now constitutes an established corpus of synthetic methods efficiently complementing biological approaches. One factor explaining this spectacular evolution is the emergence of a new class of chemoselective reactions enabling the formation of native peptide bonds between two unprotected peptidic segments, also known as native ligation reactions. In recent years, their application has fueled the production of homogeneous batches of large and highly decorated protein targets with a control of their composition at the atomic level. In doing so, native ligation reactions have provided the means for successful applications in chemical biology, medicinal chemistry, materials science, and nanotechnology research. The native chemical ligation (NCL) reaction has had a major impact on the field by enabling the chemoselective formation of a native peptide bond between a C-terminal peptidyl thioester and an N-terminal cysteinyl peptide. Since its introduction in 1994, the NCL reaction has been made the object of significant improvements and its scope and limitations have been thoroughly investigated. Furthermore, the diversification of peptide segment assembly strategies has been essential to access proteins of increasing complexity and has had to overcome the challenge of controlling the reactivity of ligation partners. One hallmark of NCL is its dependency on thiol reactivity, including for its catalysis. While Nature constantly plays with the redox properties of biological thiols for the regulation of numerous biochemical pathways, such a control of reactivity is challenging to achieve in synthetic organic chemistry and, in particular, for those methods used for assembling peptide segments by chemical ligation. This Account covers the studies conducted by our group in this area. A leading theme of our research has been the conception of controllable acyl donors and cysteine surrogates that place the chemoselective formation of amide bonds by NCL-like reactions under the control of dichalcogenide-based redox systems. The dependency of the redox potential of dichalcogenide bonds on the nature of the chalcogenides involved (S, Se) has appeared as a powerful means for diversifying the systems, while allowing their sequential activation for protein synthesis. Such a control of reactivity mediated by the addition of harmless redox additives has greatly facilitated the modular and efficient preparation of multiple targets of biological relevance. Taken together, these endeavors provide a practical and robust set of methods to address synthetic challenges in chemical protein synthesis.

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