1. Academic Validation
  2. Widening and diversifying the proteome capture by combinatorial peptide ligand libraries via Alcian Blue dye binding

Widening and diversifying the proteome capture by combinatorial peptide ligand libraries via Alcian Blue dye binding

  • Anal Chem. 2015;87(9):4814-20. doi: 10.1021/acs.analchem.5b00218.
Giovanni Candiano 1 Laura Santucci 1 Andrea Petretto 2 Chiara Lavarello 2 Elvira Inglese 2 Maurizio Bruschi 1 Gian Marco Ghiggeri 1 Egisto Boschetti 3 Pier Giorgio Righetti 4
Affiliations

Affiliations

  • 1 †Nephrology, Dialysis, Transplantation Unit and Laboratory on Pathophysiology of Uremia, Istituto Giannina Gaslini, Genoa 16148, Italy.
  • 2 ‡Core Facilities-Proteomics Laboratory, Istituto Giannina Gaslini, Genoa 16148, Italy.
  • 3 §EB JAM-Conseil, 92200 Neuilly sur-Seine, Paris, France.
  • 4 ∥Department of Chemistry, Materials and Chemical Engineering, "Giulio Natta", Politecnico di Milano, Via Mancinelli 7, Milano 20131, Italy.
Abstract

Combinatorial peptide ligand libraries (CPLLs) tend to bind complex molecules such as dyes due to their aromatic, heterocyclic, hydrophobic, and ionic nature that may affect the protein capture specificity. In this experimental work Alcian Blue 8GX, a positively charged phthalocyanine dye well-known to bind to glycoproteins and to glucosaminoglycans, was adsorbed on a chemically modified CPLL solid phase, and the behavior of the resulting conjugate was then investigated. The control and dye-adsorbed beads were used to harvest the human urinary proteome at physiological pH, this resulting in a grand total of 1151 gene products identified after the capture. Although the Alcian Blue-modified CPLL incremented the total protein capture by 115 species, it particularly enriched some families among the harvested proteins, such as glycoproteins and nucleotide-binding proteins. This study teaches that it is possible, via the two combined harvest mechanisms, to drive the CPLL capture toward the enrichment of specific protein categories.

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