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Resolving sulfation PTMs on a plant peptide hormone using nanopore sequencing.
Chen, Xiuqi; van de Sande, Jasper W; Ritmejeris, Justas; Wen, Chenyu; Brinkerhoff, Henry; Laszlo, Andrew H; Albada, Bauke; Dekker, Cees.
Afiliação
  • Chen X; Department of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology, Delft, the Netherlands.
  • van de Sande JW; These authors contributed equally.
  • Ritmejeris J; Laboratory of Organic Chemistry, Wageningen University & Research, Wageningen, the Netherlands.
  • Wen C; These authors contributed equally.
  • Brinkerhoff H; Department of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology, Delft, the Netherlands.
  • Laszlo AH; These authors contributed equally.
  • Albada B; Department of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology, Delft, the Netherlands.
  • Dekker C; Department of Physics, University of Washington, Seattle, WA, USA.
bioRxiv ; 2024 May 10.
Article em En | MEDLINE | ID: mdl-38765996
ABSTRACT
Peptide phytohormones are decorated with post-translational modifications (PTMs) that are crucial for receptor recognition. Tyrosine sulfation on these hormones is essential for plant growth and development1. Measuring the occurrence and position of sulfotyrosine is, however, compromised by major technical challenges during isolation and detection2. We recently introduced a nanopore peptide sequencing method that sensitively detects PTMs at the single-molecule level3. By translocating PTM variants of the plant pentapeptide hormone phytosulfokine (PSK) through a nanopore, we here demonstrate accurate identification of sulfation and phosphorylation on the two tyrosine residues of PSK. Sulfation can be clearly detected and distinguished (>90%) from phosphorylation on the same residue. Moreover, the presence or absence of PTMs on the two close-by tyrosine residues can be accurately determined (>96% accuracy). Our findings demonstrate the extraordinary sensitivity of nanopore protein measurements, providing a new tool for identifying sulfation on peptide phytohormones and promising wider applications to identify protein PTMs.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda
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