Large‐scale top‐down proteomics of the Arabidopsis thaliana leaf and chloroplast proteomes. Issue 3 (1st October 2022)

• Record Type: Journal Article
• Authors: Wang, Qianjie; Sun, Liangliang; Lundquist, Peter Knut
• Other Names: Liu Yansheng guestEditor.; Salovska Barbora guestEditor.
• Is Part Of: Proteomics. Volume 23:Issue 3/4(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-10-01
• Subjects: Arabidopsis thaliana -- chloroplast -- mass spectrometry -- post‐translational modifications -- proteoform -- singlet oxygen -- top‐down proteomics -- transit peptide; Proteins -- Separation -- Periodicals; Bioinformatics -- Periodicals; Proteomics -- Periodicals; Genomes -- Periodicals; Molecular genetics -- Periodicals; 572.605
• DOI: 10.1002/pmic.202100377
• Languages: English
• ISSNs: 1615-9853

Abstract

Abstract: We present a large‐scale top‐down proteomics (TDP) study of plant leaf and chloroplast proteins, achieving the identification of over 4700 unique proteoforms. Using capillary zone electrophoresis coupled with tandem mass spectrometry analysis of offline size‐exclusion chromatography fractions, we identify 3198 proteoforms for total leaf and 1836 proteoforms for chloroplast, with 1024 and 363 proteoforms having post‐translational modifications, respectively. The electrophoretic mobility prediction of capillary zone electrophoresis allowed us to validate post‐translational modifications that impact the charge state such as acetylation and phosphorylation. Identified modifications included Trp (di)oxidation events on six chloroplast proteins that may represent novel targets of singlet oxygen sensing. Furthermore, our TDP data provides direct experimental evidence of the N‐ and C‐terminal residues of numerous mature proteoforms from chloroplast, mitochondria, endoplasmic reticulum, and other sub‐cellular localizations. With this information, we suggest true transit peptide cleavage sites and correct sub‐cellular localization signal predictions. This large‐scale analysis illustrates the power of top‐down proteoform identification of post‐translational modifications and intact sequences that can benefit our understanding of both the structure and function of hundreds of plant proteins.