TY - JOUR
T1 - Spatiotemporally confined red light-controlled gene delivery at single-cell resolution using adeno-associated viral vectors
AU - Hörner, Maximilian
AU - Jerez-Longres, Carolina
AU - Hudek, Anna
AU - Hook, Sebastian
AU - Yousefi, O. Sascha
AU - Schamel, Wolfgang W.A.
AU - Hörner, Cindy
AU - Zurbriggen, Matias D.
AU - Ye, Haifeng
AU - Wagner, Hanna J.
AU - Weber, Wilfried
N1 - Publisher Copyright:
Copyright © 2021 The Authors, some rights reserved.
PY - 2021/6
Y1 - 2021/6
N2 - Methodologies for the controlled delivery of genetic information into target cells are of utmost importance for genetic engineering in both fundamental and applied research. However, available methods for efficient gene transfer into user-selected or even single cells suffer from low throughput, the need for complicated equipment, high invasiveness, or side effects by off-target viral uptake. Here, we engineer an adeno-associated viral (AAV) vector system that transfers genetic information into native target cells upon illumination with cell-compatible red light. This OptoAAV system allows adjustable and spatially resolved gene transfer down to single-cell resolution and is compatible with different cell lines and primary cells. Moreover, the sequential application of multiple OptoAAVs enables spatially resolved transduction with different transgenes. The approach presented is likely extendable to other classes of viral vectors and is expected to foster advances in basic and applied genetic research.
AB - Methodologies for the controlled delivery of genetic information into target cells are of utmost importance for genetic engineering in both fundamental and applied research. However, available methods for efficient gene transfer into user-selected or even single cells suffer from low throughput, the need for complicated equipment, high invasiveness, or side effects by off-target viral uptake. Here, we engineer an adeno-associated viral (AAV) vector system that transfers genetic information into native target cells upon illumination with cell-compatible red light. This OptoAAV system allows adjustable and spatially resolved gene transfer down to single-cell resolution and is compatible with different cell lines and primary cells. Moreover, the sequential application of multiple OptoAAVs enables spatially resolved transduction with different transgenes. The approach presented is likely extendable to other classes of viral vectors and is expected to foster advances in basic and applied genetic research.
UR - https://www.scopus.com/pages/publications/85108021916
U2 - 10.1126/sciadv.abf0797
DO - 10.1126/sciadv.abf0797
M3 - 文章
C2 - 34134986
AN - SCOPUS:85108021916
SN - 2375-2548
VL - 7
JO - Science Advances
JF - Science Advances
IS - 25
M1 - abf0797
ER -