Mechanism of cytotoxicity of ricin

蓖麻毒素的细胞毒性机制

• 批准号: 7268232
• 负责人: NILGUN E TUMER
• 金额: $ 35.32万
• 依托单位: RUTGERS, THE STATE UNIV OF N.J.
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-03-15 至 2012-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7268232
• 关键词: Address; Adenine; Aerosols; Affect; Antidotes; Apoptosis; Apoptotic; Binding; Biochemical; Biological Models; Biological Warfare; Bioterrorism; Breathing; Categories; Cell Death; Cells; Cessation of life; Cytosol; Defect; Depurination; Development; Endocytosis; Endoplasmic Reticulum; Enterotoxins; Genes; Genome; Genomics; Induction of Apoptosis; Intoxication; Lectin; Lung; MAPK14 gene; MAPK8 gene; Mammalian Cell; Measures; Medical; Membrane; Messenger RNA; Molecular; Mutagenesis; N glycosidase; National Institute of Allergy and Infectious Disease; Plants; Plasmids; Process; Protein Biosynthesis; Protein Synthesis Inhibition; Proteins; RNA Splicing; Resistance; Respiratory System; Ribosomal RNA; Ribosomes; Ricin; Ricinus communis; Risk; Role; Signal Pathway; Signal Transduction; Small Interfering RNA; System; Techniques; Terrorism; Toxin; Translations; Vaccines; Yeasts; base; biodefense; cell injury; cell killing; cytotoxicity; design; instrument; mutant; novel therapeutics; prevent; prototype; response; ribosomal A-protein

DESCRIPTION (provided by applicant): Ribosome inactivating proteins (RIPs) have been used as instruments of biological warfare and terrorism. Ricin is a heterodimeric plant toxin that consists of A and B-chains and the prototype of type II RIPs. Its B- chain is a lectin that enables cell binding. After endocytosis, the A-chain translocates through the endoplasmic reticulum membrane to reach the cytosol where its N-glycosidase activity removes a specific adenine from the highly conserved, sarcin/ricin loop (SRL) in the large rRNA. Ricin has been classified as Category B priority for biodefense. Very little is known about the membrane translocation and ribosome interactions of ricin and the molecular mechanism by which it causes apoptosis in mammalian cells. We have established yeast as a biologically relevant model system to study the activity of RTA, and isolated mutant forms of RTA, which do not kill cells. Translation inhibition by ribosome depurination has been hypothesized to be responsible for the cytotoxicity of ricin. However, our preliminary analysis of the nontoxic RTA mutants indicates that ribosome depurination is not sufficient for cytotoxicity. This project aims to use yeast and mammalian cells as complementary systems to understand the molecular basis for ricin intoxication. Specific Aims: 1. Using the nontoxic RTA mutants, determine if ribosome binding and depurination are required for cytotoxicity in yeast and induction of apoptosis in mammalian cells. 2. Characterize the interaction between RTA and ribosomal protein PO and determine if binding to PO is essential for ribosome depurination by RTA. 3. Identify the cellular genes necessary for cytotoxicity of RTA in yeast and determine if RTA causes cell death by affecting induction of the unfolded protein response (UPR). Ricin is not only a bioterrorism threat, but inhibits translation by a similar mechanism as the bacterial enterotoxins. Therefore, the studies outlined in this application will have important implications for the design of protection strategies against AB-toxins that are classified as high-risk candidates for bioterrorism.

描述（由申请人提供）：核糖体失活蛋白（RIP）已被用作生物战和恐怖主义的工具。蓖麻毒素是一种异二聚体植物毒素，由 A 链和 B 链组成，是 II 型 RIP 的原型。它的 B 链是一种能够实现细胞结合的凝集素。内吞作用后，A 链易位穿过内质网膜到达胞质溶胶，其中其 N-糖苷酶活性从大 rRNA 中高度保守的肌氨酸/蓖麻毒素环 (SRL) 中去除特定的腺嘌呤。蓖麻毒素已被列为生物防御 B 类优先级。关于蓖麻毒素的膜易位和核糖体相互作用及其引起哺乳动物细胞凋亡的分子机制知之甚少。我们建立了酵母作为生物学相关的模型系统来研究RTA的活性，并分离出不杀死细胞的RTA突变形式。推测核糖体脱嘌呤的翻译抑制是造成蓖麻毒素细胞毒性的原因。然而，我们对无毒 RTA 突变体的初步分析表明，核糖体脱嘌呤不足以产生细胞毒性。该项目旨在利用酵母和哺乳动物细胞作为补充系统来了解蓖麻毒素中毒的分子基础。具体目标： 1. 使用无毒的 RTA 突变体，确定酵母细胞毒性和哺乳动物细胞凋亡诱导是否需要核糖体结合和脱嘌呤。 2. 表征 RTA 和核糖体蛋白 PO 之间的相互作用，并确定与 PO 的结合对于 RTA 核糖体脱嘌呤是否至关重要。 3. 鉴定酵母中 RTA 细胞毒性所需的细胞基因，并确定 RTA 是否通过影响未折叠蛋白反应 (UPR) 的诱导而导致细胞死亡。蓖麻毒素不仅是一种生物恐怖主义威胁，而且通过与细菌肠毒素类似的机制抑制翻译。因此，本申请中概述的研究将对设计针对被归类为生物恐怖主义高风险候选物的 AB 毒素的保护策略具有重要意义。