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SENDing CRISPR & other RNA tools into cells
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One of the major challenges for RNA therapeutics (like CRISPR-Cas9) is delivery - making sure it is efficient, safe and selective - it targets the cells you want it to.
Two mechanisms to achieve this are adeno-associated viruses (AAVs) and lipid nanoparticles.
But now, there may be a third. Bring on selective endogenous encapsidation for cellular delivery or SEND, as much easier to say. Developed in Feng Zhang's lab they show that PEG10 an endogenous retroelement can be exploited to develop an modular RNA delivery tool to transfer RNA between cells.
I explain my understanding of SEND and its potential applications e.g for CRISPR-Cas9 delivery in this video. (so SENDing CRISPR and other RNA tools into cells)
REFERENCES;
Two mechanisms to achieve this are adeno-associated viruses (AAVs) and lipid nanoparticles.
But now, there may be a third. Bring on selective endogenous encapsidation for cellular delivery or SEND, as much easier to say. Developed in Feng Zhang's lab they show that PEG10 an endogenous retroelement can be exploited to develop an modular RNA delivery tool to transfer RNA between cells.
I explain my understanding of SEND and its potential applications e.g for CRISPR-Cas9 delivery in this video. (so SENDing CRISPR and other RNA tools into cells)
REFERENCES;
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