Design, synthesis, and characterization of new cyclic d,l-α-alternate amino acid peptides by capillary electrophoresis coupled to electrospray ionization mass spectrometry

• Published in: Analytical biochemistry Vol. 502; pp. 8 - 15
• Main Authors: Cortez-Díaz, María Dámaris, d’Orlyé, Fanny, Gutierrez-Granados, Silvia, de Leon-Rodriguez, Luis Manuel, Varenne, Anne
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.06.2016; Elsevier Masson
• Subjects: Amino Acids - chemistry; Capillary electrophoresis; Chemical Sciences; Cyclic peptides; Drug Design; Electrophoresis, Capillary; Electrospray ionization; Engineering Sciences; Life Sciences; Mass spectrometry; Molecular Conformation; Peptide nanotubes; Peptides, Cyclic - chemical synthesis; Peptides, Cyclic - chemistry; Purity; Spectrometry, Mass, Electrospray Ionization; UV; BGE; CE; DG; Capillary electrophoresis; Cyclic peptides; Electrospray ionization; MS; Purity; CNT; ACN; CP; TFA; TIC; SIM; PNT; Peptide nanotubes; NG; ESI; DMF; Mass spectrometry; HPLC
• ISSN: 0003-2697; 1096-0309
• DOI: 10.1016/j.ab.2016.02.021

The self-assembly of peptide nanotubes (PNTs) depends on the structure and chemistry of cyclic peptide (CP) monomers, having an impact on their properties, making the choice of their monomers and their characterization a great challenge. We synthesized for the first time a new set of eight original CP sequences of 8, 10, and 12 d,l-α-alternate amino acids with a controlled internal diameter from 7 to 13 Å. They present various properties (e.g., diameter, global surface charge, hydrophobicity) that can open the way to new applications. Their structure and purity were determined thanks to a capillary electrophoresis coupled to electrospray ionization mass spectrometry (CE–ESI–MS) methodology developed for the first time for this purpose. The CPs were successfully separated in a basic hydro-organic background electrolyte (BGE, pH 8.0, H2O/EtOH 50:50, v/v) and analyzed in MS positive mode. The effect of CP structure on electrophoretic mobility was studied, and the mass spectra were deeply analyzed. This methodology allowed verifying their purity and the absence of linear peptide precursors as well as their stability when stored over several months. Therefore, we have developed a new CE–ESI–MS methodology for the structure and purity control of interesting potential precursors for PNTs that could be employed as nanoplatforms in diagnostics or as pseudo sieving tools for separative purposes.