Separation of proteins by cation-exchange sequential injection chromatography using a polymeric monolithic column

Autor(es)

Masini, Jorge Cesar

• Tipo de documento: Artigo Científico
• Fonte: ANALYTICAL AND BIOANALYTICAL CHEMISTRY; v. 408, n. 5, p. 1445-1452, FEB 2016.
• Citações Web of Science: 11

Resumo

Since sequential injection chromatography (SIC) emerged in 2003, it has been used for separation of small molecules in diverse samples, but separations of high molar mass compounds such as proteins have not yet been described. In the present work a poly(glycidyl methacrylate-co-ethylene dimethacrylate) (GMA-co-EDMA) monolithic column was prepared by free radical polymerization inside a 2.1-mm-i.d. activated fused silica-lined stainless steel tubing and modified with iminodiacetic acid (IDA). The column was prepared from a mixture of 24 % GMA, 16 % EDMA, 20 % cyclohexanol, and 40 % 1-dodecanol (all % as w/w) containing 1 % of azobisisobutyronitrile (AIBN) (in relation to monomers). Polymerization was done at 60 A degrees C for 24 h. The polymer was modified with 1.0 M IDA (in 2 M Na2CO3, pH 10.5) at 80 A degrees C for 16 h. Separation of myoglobin, ribonuclease A, cytochrome C, and lysozyme was achieved at pH 7.0 (20 mM KH2PO4/K2HPO4) using a salt gradient (NaCl). Myoglobin was not retained, and the other proteins were separated by a gradient of NaCl created inside the holding coil (4 m of 0.8-mm-i.d. PTFE tubing) by sequential aspiration of 750 and 700 mu L of 0.2 and 0.1 M NaCl, respectively. As the flow was reversed toward the column (5 mu L s(-1)) the interdispersion of these solutions created a reproducible gradient which separated the proteins in 10 min, with the following order of retention: ribonuclease A < cytochrome C < lysozyme. The elution order was consistent with a cation-exchange mechanism as the retention increased with the isoelectric points. (AU)

• Processo FAPESP: 13/18507-4 - Materiais monolíticos porosos para separações cromatográficas e preparo de amostras
• Beneficiário: Jorge Cesar Masini
• Modalidade de apoio: Auxílio à Pesquisa - Regular