TRYPANOSOMA FLAGELLUM

鞭毛锥虫

• 批准号: 7953812
• 负责人: Cynthia He
• 金额: $ 3.48万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-12-01 至 2009-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7953812
• 关键词: Affect; Biological; Computer Retrieval of Information on Scientific Projects Database; Defect; Electron Microscopy; Flagella; Funding; Grant; Growth; Institution; Organelles; Parasites; Pathogenesis; Proteins; RNA Interference; Research; Research Personnel; Resources; Sequence Analysis; Source; Trypanosoma; Trypanosoma brucei brucei; United States National Institutes of Health; cell motility; interest; macromolecule; retinal rods

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The T. brucei flagellum is a multi-component, multifunctional organelle critical for pathogenesis. Flagellum in Trypanosoma brucei contains not only the classic "9+2" axoneme but also a crystalline paraflagellar rod (PFR). The biological interest in this project is the structural organization of the two major structural components of PFR which have been characterized, PFR1 and PFR2 at 69KD and 73KD, respectively (Deflorin et al., 1994). They appear by sequence analysis to consist largely of coiled-coil motifs. Depletion of one PFR protein by RNA interference did not affect parasite growth or division nor formation of the axoneme. But it completely abolished the assembly of the PFR, resulting in defects in cell motility and infectivity (Bastin et al., 1998; Bastin et al., 1999).

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 霸王布鲁氏菌鞭毛是一种多组分、多功能的细胞器，对致病至关重要。布氏锥虫的鞭毛除具有典型的“9+2”轴丝外，还具有一个结晶状的副鞭毛杆（PFR）。该项目中的生物学兴趣是PFR的两个主要结构组分的结构组织，其已被表征，分别为69 KD和73 KD的PFR 1和PFR 2（Deforin等人，1994年）。通过序列分析，它们似乎主要由卷曲螺旋基序组成。通过RNA干扰耗尽一种PFR蛋白并不影响寄生虫的生长或分裂，也不影响轴丝的形成。但它完全消除了PFR的组装，导致细胞运动性和感染性的缺陷（Bastin et al.，1998; Bastin等人，1999年）。