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Aside from these examples, little is known about the biophysical impact of many other sitespecific posttranslational modifications on apoSOD1 stability, despite numerous solventaccessible sites for glutathionylation, acetylation, glycation, phosphorylation, succinylation and ubiquitylation (Figure 9).[ 62 , 72 , 86 , 120b , 124 ] Advances in this area will require greater refinement of emerging methodologies designed to target certain modifications to specific protein residues in vitro and in vivo, [132] including selective chemical modification of proteins, protein semisynthesis, native chemical ligation, and the genetic noncanonical amino acid incorporation approach

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doi: 10.3389/fimmu.2024.1424954 116 LiCLiuJHouWKangRTangD

Regulatory mechanisms involved in activator-protein-1 (AP-1)-mediated activation of glutathione S-transferase gene expression by chemical agents