PMID- 35980581 OWN - NLM STAT- MEDLINE DCOM- 20220822 LR - 20220914 IS - 1940-6029 (Electronic) IS - 1064-3745 (Linking) VI - 2540 DP - 2022 TI - Anchor Away: A System for Fast Inhibition of Proteins in Drosophila. PG - 239-249 LID - 10.1007/978-1-0716-2541-5_11 [doi] AB - Anchor away is a sequestering method designed to acutely and timely abrogate the function of a protein of interest by anchoring to a cell compartment different from its target. This method induces the binding of the target protein to the anchor by either the addition of rapamycin to Drosophila food or cell media. Rapamycin mediates the formation of a ternary complex between the anchor, which is tagged with the FK506-binding protein (FKBP12), and the target protein fused with the FKB12 rapamycin-binding (FRB) domain of mammalian target of rapamycin (mTOR). The rapamycin-bound target protein stays sequestered away from its compartment, where it cannot perform its biological function. CI - (c) 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature. FAU - Sanchez Bosch, Pablo AU - Sanchez Bosch P AD - Stanford University School of Medicine, Stanford, CA, USA. pablosb@stanford.edu. LA - eng PT - Journal Article PL - United States TA - Methods Mol Biol JT - Methods in molecular biology (Clifton, N.J.) JID - 9214969 RN - EC 5.2.1.- (Tacrolimus Binding Protein 1A) RN - EC 5.2.1.- (Tacrolimus Binding Proteins) RN - W36ZG6FT64 (Sirolimus) SB - IM MH - Animals MH - *Drosophila/metabolism MH - Mammals/metabolism MH - *Sirolimus/pharmacology MH - Tacrolimus Binding Protein 1A/metabolism MH - Tacrolimus Binding Proteins OTO - NOTNLM OT - CRISPR OT - Loss of function OT - Protein knockout OT - Rapamycin OT - TOR EDAT- 2022/08/19 06:00 MHDA- 2022/08/23 06:00 CRDT- 2022/08/18 11:21 PHST- 2022/08/18 11:21 [entrez] PHST- 2022/08/19 06:00 [pubmed] PHST- 2022/08/23 06:00 [medline] AID - 10.1007/978-1-0716-2541-5_11 [doi] PST - ppublish SO - Methods Mol Biol. 2022;2540:239-249. doi: 10.1007/978-1-0716-2541-5_11.