Researchers uncover mechanism for how common gene therapy vectors enter cells

(Massachusetts Eye and Ear Infirmary) Researchers have identified a novel cellular entry factor for adeno-associated virus vector (AAV) types -- the most commonly used viral vectors for in vivo gene therapy. The researchers identified that GPR108, a G protein-coupled receptor, served as a molecular 'lock' to the cell. The discovery could one day enable scientists to better direct AAV gene transfers to specific tissues.
Source: EurekAlert! - Biology - Category: Biology Source Type: news