Reduction of protein concentration range difference followed by multicolumn fractionation prior to 2-DE and LC-MS/MS profiling of serum proteins

• Published in: Electrophoresis Vol. 32; no. 6-7; pp. 674 - 685
• Main Authors: Selvaraju, Subhashini, El Rassi, Ziad
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag 01.03.2011; WILEY‐VCH Verlag
• Subjects: 2-DE; affinity chromatography; Beads; benzene; blood proteins; Blood Proteins - analysis; Blood Proteins - metabolism; blood serum; Chromatography, Affinity - methods; Chromatography, Reverse-Phase; Copper; Distillation; electrophoresis; Electrophoresis, Gel, Two-Dimensional - methods; Equalization; Equalizers; Fractionation; Humans; Immobilized metal ion affinity chromatography; metal ions; Nickel; Peptide Fragments - analysis; Peptide Fragments - classification; Peptide Fragments - metabolism; Peptide Library; polystyrenes; Proteins; Proteomics; Proteomics - methods; ProteoMiner; Reduction; Serums; Tandem Mass Spectrometry - methods; Trypsin - metabolism; Zinc
• ISSN: 0173-0835; 1522-2683; 1522-2683
• DOI: 10.1002/elps.201000606

This article is concerned with the reduction of protein concentration range differences by the peptide beads library technology (ProteoMiner™ or “equalizer” technology), which in principle allows the enrichment of proteins to the same concentration level (i.e. protein equalizer) regardless of the original protein abundance in a given biological fluid such as human serum, which is the subject of our investigation. After the equalization step, the captured proteins from human serum were fractionated on a series of tandem monolithic columns with surface‐bound iminodiacetic acid ligands to which three different metal ions, namely, Zn2+, Ni2+ and Cu2+ were immobilized to yield the so‐called immobilized metal affinity chromatography columns. These three monolithic columns were connected to a reversed‐phase column packed with polystyrene divinyl benzene beads. Aliquots taken from the four collected fractions from the four tandem columns were subsequently fractionated by 2‐DE. Also, aliquots from the four collected fractions were tryptically digested and analyzed by LC‐MS/MS. The strategy of subsequent fractionation on the four tandem columns after equalization allowed the identification of more proteins than simply using the equalization by ProteoMiner™. The equalizer technology was compared to the immuno‐subtraction approach. While the ProteoMiner™ technology is superior in terms of the overall number of captured proteins, it only complements the immuno‐subtraction approach since the latter can capture the proteins that were not captured by the former.