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Table 2 EV modifications for loading CRISPR/Cas components

From: Current and prospective strategies for advancing the targeted delivery of CRISPR/Cas system via extracellular vesicles

Modification strategy of EVs

Loading mechanism

Disassembly mechanism

Model

References

Bioengineering

GFP-CD63 fused with Cas9-antiGFP nanobody

/

In vitro

[29, 177]

CD63-com fused with ABP Com-sgRNA

/

In vivo

[40]

ARRDC1 fused with WW-Cas9

/

In vivo

[47]

CD9-HuR and ABE-AU-mRNA interaction

/

In vitro, in vivo

[29]

VSV-G-assisted

Spontaneous release

In vivo, in vitro

[35, 50]

split GFP complementation

/

In vitro, in vivo

[48]

chemical-induced incorporation

/

In vitro, in vivo

[36]

CD9-CIBN and Cas9-CRY2 interaction, light

Removal of the light

In vivo

[46]

Physical method (Freeze–thaw, sonication)

TDNs-EVs

/

In vitro, in vivo

[22]

Physical method (Freeze–thaw, co-incubation)

Multivalent electrostatic interaction

/

In vivo

[9, 18]