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细菌信号转导系统的功能注释:进展与挑战

Functional Annotation of Bacterial Signal Transduction Systems: Progress and Challenges.

机构信息

Department of Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Prof. Albareda 1, 18008 Granada, Spain.

Department of Biochemistry and Molecular Biology 'B' and Immunology, Faculty of Chemistry, University of Murcia, Campus of Espinardo, Regional Campus of International Excellence "Campus Mare Nostrum", 30100 Murcia, Spain.

出版信息

Int J Mol Sci. 2018 Nov 26;19(12):3755. doi: 10.3390/ijms19123755.

Abstract

Bacteria possess a large number of signal transduction systems that sense and respond to different environmental cues. Most frequently these are transcriptional regulators, two-component systems and chemosensory pathways. A major bottleneck in the field of signal transduction is the lack of information on signal molecules that modulate the activity of the large majority of these systems. We review here the progress made in the functional annotation of sensor proteins using high-throughput ligand screening approaches of purified sensor proteins or individual ligand binding domains. In these assays, the alteration in protein thermal stability following ligand binding is monitored using Differential Scanning Fluorimetry. We illustrate on several examples how the identification of the sensor protein ligand has facilitated the elucidation of the molecular mechanism of the regulatory process. We will also discuss the use of virtual ligand screening approaches to identify sensor protein ligands. Both approaches have been successfully applied to functionally annotate a significant number of bacterial sensor proteins but can also be used to study proteins from other kingdoms. The major challenge consists in the study of sensor proteins that do not recognize signal molecules directly, but that are activated by signal molecule-loaded binding proteins.

摘要

细菌拥有大量的信号转导系统,用于感知和响应不同的环境线索。这些系统通常是转录调节剂、双组分系统和化学感觉途径。信号转导领域的一个主要瓶颈是缺乏能够调节大多数这些系统活性的信号分子的信息。我们在这里回顾了使用纯化的传感器蛋白或单个配体结合结构域的高通量配体筛选方法对传感器蛋白进行功能注释所取得的进展。在这些测定中,使用差示扫描荧光法监测配体结合后蛋白质热稳定性的变化。我们通过几个例子来说明,识别传感器蛋白配体如何有助于阐明调节过程的分子机制。我们还将讨论使用虚拟配体筛选方法来识别传感器蛋白配体。这两种方法都已成功地应用于对大量细菌传感器蛋白进行功能注释,但也可用于研究来自其他王国的蛋白质。主要的挑战在于研究那些不直接识别信号分子但被信号分子装载的结合蛋白激活的传感器蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c85/6321045/d45bcceb94b3/ijms-19-03755-g001.jpg

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