De novo sequencing of two novel peptides homologous to calcitonin-like peptides, from skin secretion of the Chinese Frog, Odorrana schmackeri

peer-reviewed · EuPA Open Proteomics · 2015

peer-reviewed · EuPA Open Proteomics · 2015. Geisa P.C. Evaristo et al. An MS/MS based analytical strategy was followed to solve the complete sequence of two new peptides from frog…
Date 2015-09-01
Type peer-reviewed
Venue EuPA Open Proteomics
Publisher Elsevier BV
Contribution downstream-application
DOI 10.1016/j.euprot.2015.07.008
Citations (OpenAlex) 4

Abstract

An MS/MS based analytical strategy was followed to solve the complete sequence of two new peptides from frog (Odorrana schmackeri) skin secretion. This involved reduction and alkylation with two different alkylating agents followed by high resolution tandem mass spectrometry. De novo sequencing was achieved by complementary CID and ETD fragmentations of full-length peptides and of selected tryptic fragments. Heavy and light isotope dimethyl labeling assisted with annotation of sequence ion series. The identified primary structures are GCD[I/L]STCATHN[I/L]VNE[I/L]NKFDKSKPSSGGVGPESP-NH 2 and SCNLSTCATHNLVNELNKFDKSKPSSGGVGPESF-NH 2 , i.e. two carboxyamidated 34 residue peptides with an aminoterminal intramolecular ring structure formed by a disulfide bridge between Cys 2 and Cys 7 . Edman degradation analysis of the second peptide positively confirmed the exact sequence, resolving I/L discriminations. Both peptide sequences are novel and share homology with calcitonin , calcitonin gene related peptide (CGRP) and adrenomedullin from other vertebrates. Detailed sequence analysis as well as the 34 residue length of both O. schmackeri peptides, suggest they do not fully qualify as either calcitonins (32 residues) or CGRPs (37 amino acids) and may justify their classification in a novel peptide family within the calcitonin gene related peptide superfamily. Smooth muscle contractility assays with synthetic replicas of the S–S linked peptides on rat tail artery, uterus, bladder and ileum did not reveal myotropic activity.

Authors

  1. Geisa P.C. Evaristo · Delft University of Technology
  2. Martijn W. H. Pinkse · Delft University of Technology
  3. Tianbao Chen · Queen’s University Belfast
  4. Lei Wang (Queen’s University Belfast) · Queen’s University Belfast
  5. Shabaz Mohammed · Netherlands Proteomics Centre, Utrecht University
  6. Albert J. R. Heck · Center for Biomedical Genetics, Netherlands Proteomics Centre, Utrecht University
  7. Isabella Mathes · Max Planck Institute of Biochemistry
  8. Friedrich Lottspeich · Max Planck Institute of Biochemistry
  9. Chris Shaw · Queen’s University Belfast
  10. Juan Pablo Albar · Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas
  11. Peter D. E. M. Verhaert · Delft University of Technology, Lund University, University of Antwerp

Methods and tools

  • Odorrana schmackeri calcitonin-like peptides: Determined the complete sequences of two new 34-residue calcitonin-like peptides from Chinese frog skin secretion by de novo MS/MS using CID and ETD, differential alkylation and isotope dimethyl labeling.

Methods it uses

Cites (1)

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