Cell membrane coating strategies have been increasingly
researched
due to their unique capabilities of biomimicry and biointerfacing,
which can mimic the functionality of the original source cells in vivo but fail to provide customized nanoparticle surfaces
with new or enhanced capabilities beyond natural cells. However, the
field of drug lead discovery necessitates the acquisition of sufficient
surface density of specific target membrane receptors, presenting
a heightened demand for this technology. In this study, we developed
a novel approach to fabricate high density of fibroblast growth factor
receptor 4 (FGFR4) cell membrane-coated nanoparticles through covalent
site-specific immobilization between genetically engineered FGFR4
with HaloTag anchor on cell membrane and chloroalkane-functionalized
magnetic nanoparticles. This technique enables efficient screening
of tyrosine kinase inhibitors from natural products. And the enhanced
density of FGFR4 on the surface of nanoparticles were successfully
confirmed by Western blot assay and confocal laser scanning microscopy.
Further, the customized nanoparticles demonstrated exceptional sensitivity
(limit of detection = 0.3 × 10–3 μg mL–1). Overall, the proposed design of a high density
of membrane receptors, achieved through covalent site-specific immobilization
with a HaloTag anchor, demonstrates a promising strategy for the development
of cell membrane surface engineering. This approach highlights the
potential of cell membrane coating technology for facilitating the
advanced extraction of small molecules for drug discovery.