| Literature DB >> 34978789 |
Erin E Berlew1, Keisuke Yamada1,2, Ivan A Kuznetsov1, Eleanor A Rand1,3, Chandler C Ochs1,4, Zaynab Jaber5,6, Kevin H Gardner5,7,8, Brian Y Chow1.
Abstract
We describe the efficient creation of single-component optogenetic tools for membrane recruitment-based signaling perturbation using BcLOV4 technology. The workflow requires two plasmids to create six different domain arrangements of the dynamic membrane binder BcLOV4, a fluorescent reporter, and the fused signaling protein of interest. Screening of this limited set of genetic constructs for expression characteristics and dynamic translocation in response to one pulse of light is sufficient to identify viable signaling control tools. The reliability of this streamlined approach is demonstrated by the creation of an optogenetic Cdc42 GTPase and Rac1-activating Tiam1 GEF protein, which together with our other recently reported technologies, completes a toolbox for spatiotemporally precise induction of Rho-family GTPase signaling at the GEF or GTPase level, for driving filopodial protrusions, lamellipodial protrusions, and cell contractility, respectively mediated by Cdc42, Rac1, and RhoA.Entities:
Keywords: BcLOV4; Cdc42; Rho GTPase; Tiam1; optogenetics
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Year: 2022 PMID: 34978789 PMCID: PMC8867532 DOI: 10.1021/acssynbio.1c00604
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110