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Attaching proteins, nucleic acids, or small molecules to the VLP surface, such as for targeting a specific cell type or for raising an immune response is useful. In some cases a protein of interest can be genetically fused to the viral coat protein. However, this approach sometimes leads to impaired VLP assembly and has limited utility if the targeting agent is not protein-based. An alternative is to assemble the VLP and then use chemical crosslinkers, reactive unnatural amino acids

VLP-based therapeutic vaccines for the induction of protective T cvlpells in a therapeutic regimen. VLPs decorated with T-cell epitopes are efficient tools for eliciting T H 1。

Engineered virus-like particles enhance the delivery of prime editor ribonucleoprotein complexes for efficient genomic editing in living systems.

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