4.8 Article

Magnetic Nanoplatforms for Covalent Protein Immobilization Based on Spy Chemistry

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 37, Pages 44147-44156

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c14670

Keywords

magnetic nanoparticles; spy chemistry; protein immobilization; surface polymerization; protein-polymer conjugate

Funding

  1. United States Department of Agriculture [USDA 2019-67021-29453]
  2. ND Nano Materials Science and Engineering Fellowship

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Protein immobilization on magnetic nanoparticles using the SpyTag-SpyCatcher chemistry is an effective method to enhance stability and facilitate separation. The SpyTag peptide incorporated into MNPs improves loading capacity and water dispersity, allowing for efficient and stable conjugation without the need for additional enzymes or cross-linkers. The platform offers protection and improved shelf life for immobilized proteins, with fast magnetophoresis for easy recovery under external magnetic fields.
Immobilization of proteins on magnetic nanoparticles (MNPs) is an effective approach to improve protein stability and facilitate separation of immobilized proteins for repeated use. Herein, we exploited the efficient SpyTag-SpyCatcher chemistry for conjugation of functional proteins onto MNPs and established a robust magnetic-responsive nanoparticle platform for protein immobilization. To maximize the loading capacity and achieve outstanding water dispersity, the SpyTag peptide was incorporated into the surface-charged polymers of MNPs, which provided abundant active sites for Spy chemistry while maintaining excellent colloidal stability in buffer solution. Conjugation between enhanced green fluorescence protein (EGFP)-SpyCatcher-fused proteins and SpyTag-functionalized MNPs was efficient at ambient conditions without adding enzymes or chemical cross-linkers. Benefiting from the excellent water dispersity and interface compatibility, the surface Spy reaction has fast kinetics, which is comparable to that of the solution Spy reaction. No activity loss was observed on EGFP after conjugation due to the site-selective nature of Spy chemistry. The immobilization process of EGFP on MNPs was highly specific and robust, which was not affected by the presence of other proteins and detergents, such as bovine serum albumin and Tween 20. The MNP platform was demonstrated to be protective to the conjugated EGFP and significantly improved the shelf life of immobilized proteins. In addition, experiments confirmed the retained magnetophoresis of the MNP after protein loading, demonstrating fast MNP recovery under an external magnetic field. This MNP is expected to provide a versatile and modular platform to achieve effective and specific immobilization of other functional proteins, enabling easy reuse and storage.

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