Engineering Bacteriophytochrome-coupled Photoactivated Adenylyl Cyclases for Enhanced Optogenetic cAMP Modulation

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2024-03-01 DOI:10.1016/j.jmb.2023.168257
Qianzhao Xu , Arend Vogt , Fabian Frechen , Chengwei Yi , Melike Küçükerden , Neville Ngum , Laia Sitjà-Roqueta , Andreas Greiner , Rhein Parri , Mercè Masana , Nikolaus Wenger , Dagmar Wachten , Andreas Möglich
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Abstract

Sensory photoreceptors abound in nature and enable organisms to adapt behavior, development, and physiology to environmental light. In optogenetics, photoreceptors allow spatiotemporally precise, reversible, and non-invasive control by light of cellular processes. Notwithstanding the development of numerous optogenetic circuits, an unmet demand exists for efficient systems sensitive to red light, given its superior penetration of biological tissue. Bacteriophytochrome photoreceptors sense the ratio of red and far-red light to regulate the activity of enzymatic effector modules. The recombination of bacteriophytochrome photosensor modules with cyclase effectors underlies photoactivated adenylyl cyclases (PAC) that catalyze the synthesis of the ubiquitous second messenger 3′, 5′-cyclic adenosine monophosphate (cAMP). Via homologous exchanges of the photosensor unit, we devised novel PACs, with the variant DmPAC exhibiting 40-fold activation of cyclase activity under red light, thus surpassing previous red-light-responsive PACs. Modifications of the PHY tongue modulated the responses to red and far-red light. Exchanges of the cyclase effector offer an avenue to further enhancing PACs but require optimization of the linker to the photosensor. DmPAC and a derivative for 3′, 5′-cyclic guanosine monophosphate allow the manipulation of cyclic-nucleotide-dependent processes in mammalian cells by red light. Taken together, we advance the optogenetic control of second-messenger signaling and provide insight into the signaling and design of bacteriophytochrome receptors.

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设计细菌色素耦合光激活腺苷酸环化酶以增强光遗传学 cAMP 调节能力
感光受体在自然界中比比皆是,能使生物体的行为、发育和生理适应环境光线。在光遗传学中,光感受器可以通过光对细胞过程进行时空精确、可逆和非侵入性的控制。尽管已经开发出了许多光遗传学电路,但对红光敏感的高效系统的需求仍未得到满足,因为红光对生物组织的穿透力更强。细菌细胞色素感光器能感知红光和远红光的比例,从而调节酶效应模块的活性。细菌色素光传感器模块与环化酶效应器的重组是光激活腺苷酸环化酶(PAC)的基础,PAC 催化了无处不在的第二信使 3′、5′-环磷酸腺苷(cAMP)的合成。通过光传感器单元的同源交换,我们设计出了新型 PAC,变体 DmPAC 在红光下的环化酶活性被激活了 40 倍,从而超越了以前的红光响应型 PAC。对 PHY 舌的修改调节了对红光和远红光的反应。环化酶效应器的交换为进一步增强 PAC 提供了一条途径,但需要优化与光传感器的连接。DmPAC 和一种 3′、5′-环鸟苷酸单磷酸衍生物可通过红光操纵哺乳动物细胞中依赖环核苷酸的过程。总之,我们推进了第二信使信号的光遗传学控制,并为细菌色素受体的信号和设计提供了见解。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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