Optimization of protein entrapment in affinity microcolumns using hydrazide-activated silica and glycogen as a capping agent

John Vargas-Badilla, Saumen Poddar, Shiden Azaria, Chenhua Zhang, David S. Hage

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Several approaches were compared for the entrapment of proteins within hydrazide-activated silica for use in affinity microcolumns and high performance affinity chromatography. Human serum albumin (HSA)and concanavalin A (Con A)were used as model proteins for this work. Items considered in this study included the role played by the solution volume, amount of added protein, and use of slurry vs. on-column entrapment on the levels of solute retention and extent of protein immobilization that could be obtained by means of entrapment. The levels of retention and protein immobilization were evaluated by injecting warfarin or 4-methylumbellipheryl α-D-mannopyranoside as solutes with known binding properties for HSA or Con A. Altering both the solution volume and amount of added protein led to an increase of up to 17-fold in the extent of protein immobilization for HSA in slurry-based entrapment; on-column entrapment provided an additional 3.6-fold increase in protein content vs. the optimized slurry method. Similar general trends were seen for Con A. The protein contents obtained by entrapment for HSA or Con A (i.e., up to ~87 and 46 mg/g silica, respectively)were comparable to or higher than levels reported for the covalent immobilization of these proteins onto silica. The retention of warfarin on the entrapped HSA was at least 1.7-fold higher than has been obtained under comparable support and mobile phase conditions when using covalent immobilization. These results indicated that entrapment can be an attractive alternative to covalent immobilization for proteins such as HSA and Con A, with this approach serving as a potential means for obtaining good solute binding and retention in work with affinity microcolumns or related microscale devices.

Original languageEnglish (US)
Pages (from-to)1-8
Number of pages8
JournalJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
Volume1121
DOIs
StatePublished - Jul 15 2019

Fingerprint

Glycogen
Silicon Dioxide
Serum Albumin
Immobilization
Proteins
Concanavalin A
Warfarin
Affinity chromatography
Mannose
Affinity Chromatography
Equipment and Supplies

Keywords

  • Affinity microcolumn
  • Concanavalin A
  • Entrapment
  • High performance affinity chromatography
  • Human serum albumin
  • Protein immobilization

ASJC Scopus subject areas

  • Analytical Chemistry
  • Biochemistry
  • Clinical Biochemistry
  • Cell Biology

Cite this

Optimization of protein entrapment in affinity microcolumns using hydrazide-activated silica and glycogen as a capping agent. / Vargas-Badilla, John; Poddar, Saumen; Azaria, Shiden; Zhang, Chenhua; Hage, David S.

In: Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, Vol. 1121, 15.07.2019, p. 1-8.

Research output: Contribution to journalArticle

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