A Continuous Assay Set to Screen and Characterize Novel Protein N-Acetyltransferases Unveils Rice General Control Non-repressible 5-Related N-Acetyltransferase2 Activity

• Published in: Frontiers in plant science 2022-02, Vol.13, p.832144-832144
• Main Authors: Asensio, Thomas, Dian, Cyril, Boyer, Jean-Baptiste, Rivière, Frédéric, Meinnel, Thierry, Giglione, Carmela
• Format: Article
• Language: English
• Subjects: acetylation; GNAT; modifications; N-acetyltransferase; Plant Science; rice; yeast
• ISSN: 1664-462X; 1664-462X
• DOI: 10.3389/fpls.2022.832144

Protein N-acetyltransferases (NATs) belong to the general control non-repressible 5 (Gcn5)-related N-acetyltransferases (GNATs) superfamily. GNATs catalyze the transfer of acetyl from acetyl-CoA to the reactive amine moiety of a wide range of acceptors. NAT sequences are difficult to distinguish from other members of the GNAT superfamily and there are many uncharacterized GNATs. To facilitate the discovery and characterization of new GNATs, we have developed a new continuous, non-radioactive assay. This assay is virtually independent of the substrate and can be used to get substrate specificity hints. We validated first the assay with the well-characterized NatA (SpNatA). The SpNatA kinetic parameters were determined with various peptides confirming the robustness of the new assay. We reveal that the longer the peptide substrate the more efficient the enzyme. As a proof of concept of the relevance of the new assay, we characterized a NAA90 member from rice ( ), OsGNAT2. We took advantage of an medium-scale characterization of OsGNAT2 specificity to identify and then validate several specific peptide substrates. With this assay, we reveal long-range synergic effects of basic residues on OsGNAT2 activity. Overall, this new, high-throughput assay allows better understanding of the substrate specificity and activity of any GNAT.