Molecular logics in dual sensor regulation of diguanylate cyclase activity-Phosphorylation OR blue-light activation.

IF 5.6 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Protein Science Pub Date : 2026-09-01 DOI:10.1002/pro.70765
Maximilian Fuchs, Andreas Winkler
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引用次数: 0

Abstract

Bacterial cells use multiple environmental cues to regulate levels of the second messenger cyclic dimeric GMP. This compound influences key lifestyle decisions such as motility, biofilm formation, or virulence. Although many diguanylate cyclases (DGCs) combined with various sensory domains have been studied previously, how distinct inputs are integrated within individual enzymes remains incompletely understood. Here, we investigate a cyanobacterial family of dual sensor DGCs that combine an N-terminal receiver (Rec) domain followed by a light-oxygen-voltage (LOV) domain upstream of a diguanylate cyclase (GGDEF) domain. Using in vivo activity screening and in vitro characterization, we determined how phosphorylation and blue light, individually and jointly, regulate enzymatic activity. By measuring kinetic parameters across four defined functional states, unphosphorylated or phosphorylated, in combination with dark or light states, we reveal logic gate-like behaviors. One representative, LaRldC, integrates both signals with pronounced fold-changes in activity, consistent with overall OR-type logic and with light acting as the dominant input. Our results demonstrate its function as a molecular gate coupling phosphorylation and illumination sensing to cyclic-di-GMP formation. These findings provide valuable insights into multi-signal decision-making in cyanobacteria and establish further understanding of how modular sensory domains are wired to control bacterial second-messenger signaling.

二胍酸环化酶活性双传感器调控的分子逻辑——磷酸化或蓝光激活。
细菌细胞使用多种环境信号来调节第二信使环二聚体GMP的水平。这种化合物影响关键的生活方式的决定,如运动,生物膜的形成,或毒性。尽管许多双胍酸环化酶(DGCs)与各种感觉域的结合已经被研究过,但不同的输入是如何在单个酶中整合的仍然不完全清楚。在这里,我们研究了一个蓝藻双传感器DGCs家族,它结合了一个n端接收器(Rec)结构域,随后是一个光氧电压(LOV)结构域,位于二光酰酸环化酶(GGDEF)结构域的上游。通过体内活性筛选和体外表征,我们确定了磷酸化和蓝光如何单独或共同调节酶的活性。通过测量四种定义的功能状态(未磷酸化或磷酸化)的动力学参数,结合暗态或光态,我们揭示了逻辑门样行为。LaRldC是一种代表,它将两种信号结合起来,在活动中有明显的折叠变化,与整体的or型逻辑一致,并以光作为主要输入。我们的研究结果证明了它作为分子门偶联磷酸化和光照感应的功能,以形成环二gmp。这些发现为蓝藻的多信号决策提供了有价值的见解,并进一步了解了模块化感觉域如何连接以控制细菌的第二信使信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Protein Science
Protein Science 生物-生化与分子生物学
CiteScore
12.40
自引率
1.20%
发文量
246
审稿时长
1 months
期刊介绍: Protein Science, the flagship journal of The Protein Society, is a publication that focuses on advancing fundamental knowledge in the field of protein molecules. The journal welcomes original reports and review articles that contribute to our understanding of protein function, structure, folding, design, and evolution. Additionally, Protein Science encourages papers that explore the applications of protein science in various areas such as therapeutics, protein-based biomaterials, bionanotechnology, synthetic biology, and bioelectronics. The journal accepts manuscript submissions in any suitable format for review, with the requirement of converting the manuscript to journal-style format only upon acceptance for publication. Protein Science is indexed and abstracted in numerous databases, including the Agricultural & Environmental Science Database (ProQuest), Biological Science Database (ProQuest), CAS: Chemical Abstracts Service (ACS), Embase (Elsevier), Health & Medical Collection (ProQuest), Health Research Premium Collection (ProQuest), Materials Science & Engineering Database (ProQuest), MEDLINE/PubMed (NLM), Natural Science Collection (ProQuest), and SciTech Premium Collection (ProQuest).
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