Abstract B150: STING acquired species-specific motifs to control alternative immune responses

C. O. Mann, D. King, P. Kranzusch
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Abstract

Stimulator of Interferon Genes (STING) is an adaptor protein critical for downstream signaling during recognition of mislocalized cytosolic DNA. STING activation requires recognition of a unique second messenger 2′–5′, 3′–5′ cyclic GMP–AMP (2′3′ cGAMP) synthesized by the pathogen recognition receptor cyclic GMP–AMP synthase (cGAS). Due to its broad expression in most tissues, and ability to respond to different endogenous and foreign small molecules, STING is emerging as a promising drug target for cancer immunotherapy and treatment of autoimmune diseases. However, it remains unknown how the single adaptor protein STING controls distinct transcriptional outputs leading to production of type I interferon, proinflammatory cytokine responses or autophagy. Here we present surprising evidence for the ancient origins of the cGAS-STING signaling pathway by discovery of bacterial cGAS-like enzymes and complete functional cGAS-STING pathways in lower metazoans. Our previous structural data demonstrate that human and metazoan STING proteins share a common architecture that couples ligand binding with conformational changes and allows signal activation. However, it remained unclear how alternative STING conformations control different downstream signaling outputs, and which motifs are responsible for recruitment of the downstream factors controlling each pathway. We have now combined a phylogenetic and biochemical approach to explain the conserved elements that regulate STING downstream signaling events. Our analysis identifies new immune pathway-specific regulatory motifs acquired by distinct STING species, and we are currently focused on identifying the recruited factors important for controlling human STING signaling. Together, our results explain the molecular basis for distinct STING downstream signaling, and provide new insights for the rational design of STING pathway-specific therapeutics. Citation Format: Carina C. de Oliveira Mann, David S. King, Philip J. Kranzusch. STING acquired species-specific motifs to control alternative immune responses [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr B150.
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摘要B150: STING获得物种特异性基序来控制替代免疫反应
干扰素基因刺激因子(STING)是识别错定位细胞质DNA过程中下游信号传导的关键衔接蛋白。STING激活需要识别病原体识别受体环GMP-AMP合成酶(cGAS)合成的独特的第二信使2 ' -5 ',3 ' -5 '环GMP-AMP (2 ' 3 ' cGAMP)。由于其在大多数组织中的广泛表达,以及对不同内源性和外源性小分子的反应能力,STING正在成为癌症免疫治疗和自身免疫性疾病治疗的有前景的药物靶点。然而,目前尚不清楚单个接头蛋白STING如何控制不同的转录输出,从而产生I型干扰素、促炎细胞因子反应或自噬。在这里,我们通过在低等后生动物中发现细菌cgas样酶和完整的功能cGAS-STING通路,为cGAS-STING信号通路的古老起源提供了令人惊讶的证据。我们之前的结构数据表明,人类和后生动物的STING蛋白具有共同的结构,将配体结合与构象变化结合,并允许信号激活。然而,目前尚不清楚不同的STING构象如何控制不同的下游信号输出,以及哪些基序负责招募控制每种途径的下游因子。我们现在结合了系统发育和生化方法来解释调节STING下游信号事件的保守元件。我们的分析确定了不同STING物种获得的新的免疫途径特异性调节基序,我们目前专注于确定控制人类STING信号传导的重要招募因子。总之,我们的研究结果解释了不同的STING下游信号传导的分子基础,并为合理设计STING通路特异性治疗方法提供了新的见解。引文格式:Carina C. de Oliveira Mann, David S. King, Philip J. Kranzusch。STING获得物种特异性基序来控制替代免疫反应[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要nr B150。
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