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Updated: May 9, 2026

Isolation of Labile Multi-protein Complexes by in vivo Controlled Cellular Cross-Linking and Immuno-magnetic Affinity Chromatography
Published on: March 9, 2010
Cross-Linked Reticular Magnetic Beads Immobilizing Streptavidin for Fishing the Protein of Interest with High
Yaxuan Li1, Guangyu Wang1, Yadong Zhang1
1Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
None:
Magnetic beads immobilized with affinity ligands act as a potent tool to fish the protein of interest (POI) interacting with bioactive compounds, proteins, or nucleic acids. The high loading capacity of affinity ligands is crucial to assay sensitivity. Herein, we report a simply fabricated cross-linked carboxylic magnetic bead, Fe3O4@poly(acrylic acid-co-divinylbenzene) (PAA-co-DVB), with a reticular network, exhibiting excellent magnetic response, high carboxylic functionality, and a fast reaction rate during amidation. Streptavidin (SA) is immobilized onto Fe3O4@PAA-co-DVB through the encapsulation of appropriate pores, followed by covalent binding. The obtained Fe3O4@PAA-co-DVB@SA displays a high biotin-binding capacity of 5347 pmol mg-1 and low nonspecific protein absorption with blocking. Fe3O4@PAA-co-DVB@SA shows 1.65- and 1.55-fold higher sensitivity than commercial beads and non-cross-linked beads when fishing biotinylated proteins from pig liver lysates. The mode of immobilization was further studied, and control experiments revealed that the reticular network of Fe3O4@PAA-co-DVB is indeed capable of encapsulating proteins, and the following amidation stabilizes the immobilization. Therefore, Fe3O4@PAA-co-DVB@SA is applied to two practical cases of identifying protein-protein interaction and small molecule-protein interaction. TurboID identification of suppressor-of-G2-allele-of-skp1 (SGT1) interacting protein heat shock proteins (HSP90) in N. benthamiana reveals that the POI band enriched with Fe3O4@PAA-co-DVB@SA is 7-fold denser than that of the positive control. Further verification of in vitro interaction of Mps1 (M. oryzae mitogen-activated protein kinase I) with compound A378-0, an ATP-competitive inhibitor of kinase, demonstrates a comprehensive understanding of the action mechanism and binding affinity between proteins and their interacting molecules, and shows the feasibility and sensitivity of Fe3O4@PAA-co-DVB@SA in fishing the targeted protein for universal purposes. The excellent performance in application also offers the potential of Fe3O4@PAA-co-DVB to immobilize other affinity ligands and boost its further large-scale industrial production.
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