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Amyloid-like Interactions in Yeast Cell Adhesion

酵母细胞粘附中的淀粉样蛋白样相互作用

基本信息

批准号：
7642556
负责人：
PETER N LIPKE
金额：
$ 35.33万
依托单位：
BROOKLYN COLLEGE
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-06-20 至 2012-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7642556
关键词：
Adherence Adhesions Amino Acid Sequence Amyloid Bacterial Adhesins Binding Binding Sites Bioinformatics Candida Candida albicans Cell Adhesion Cell Adhesion Molecules Cell Aggregation Cell Wall Cell surface Chronic Disease Collaborations Complex Databases Drug resistance Event Experimental Models Fungal Genome Genes Goals Immunocompromised Host Immunoglobulin Domain Individual Infection Knowledge Lead Life Cycle Stages Ligand Binding Ligands Mediating Medical Microbial Biofilms Modeling Molecular Morbidity - disease rate Mutate Open Reading Frames Outcome Pathogenesis Pathway interactions Patients Pattern Peptide Sequence Determination Peptides Preventive Property Proteins Qualifying Reagent Recording of previous events Research Role Saccharomyces cerevisiae Site Structure Surface System Tandem Repeat Sequences Tertiary Protein Structure Testing Therapeutic Agents Therapeutic Intervention Tissues Work Yeasts amyloid formation base candidemia chemical property crosslink fungus glycosylation implantable device innovation knowledge base microbial mortality mutant pathogen protein aminoacid sequence synthetic peptide

项目摘要

DESCRIPTION (provided by applicant): Cell surface adhesins mediate the first interactions of fungi with mammalian hosts, so adhesin-mediated binding is a prelude to differentiation, colonization, biofilm formation and pathogenic invasion. These events in turn lead to complications of morbidity and mortality, especially common in immunocompromised and chronic disease patients. The C. albicans Als adhesins are implicated in pathogenesis and biofilm formation. They bind to mammalian tissues, cause fungal cell aggregation, and also co-aggregate with other microbial pathogens to mediate polymicrobial infections. Als adhesins are also important in formation of persistent and drug-resistant biofilms in tissues and on indwelling devices. Our long-term goal is to understand the roles for cell adhesion proteins in fungal life cycles and pathogenesis. The central hypothesis of this proposal is that amyloid-forming sequences are a feature of biofilm-forming adhesins, and these sequences potentiate adhesion, fungal aggregation and host invasion. This hypothesis is based on our findings that Als5p causes adherence with amyloid-like features, that the purified Als5p can form authentic amyloids, and that bioinformatic analyses reveal amyloid-forming sequences in many biofilm-associated microbial adhesins. Three specific aims will test the amyloid/ biofilm hypothesis: (1) To determine the role of specific sequences in amyloid formation and microbial adherence, we will test the working hypothesis that the amyloid-forming sequences are essential for Als-mediated cellular aggregation. (2) We will test the hypothesis that these amyloid-forming sequences in Als proteins are essential for Als-initiated biofilm formation. (3) In Als proteins, glycosylated tandem repeats follow the amyloid-forming sequences, and these repeats greatly increase adhesion activity. We will therefore test the hypothesis that the peptide sequences and glycosylation patterns in the Als repeats modulate amyloid formation to promote cellular aggregation and biofilm formation. The proposed work is innovative in its conjunction of two important concepts: amyloid-like protein interactions and adherence of pathogens leading to biofilm formation. We are also the first group to work on structure and function of Thr-rich repeat sequences in pathogenic and other fungal adhesins. Completion of these aims will lead to better defined models for the initial events in biofilm formation, and will discover whether amyloid-forming sequences are essential for biofilm adherence in fungi. If the hypothesis is supported, the results will establish connections between searches for anti-biofilm and anti-amyloid therapeutic agents.

描述（由申请人提供）：细胞表面粘附素介导真菌与哺乳动物宿主的第一次相互作用，因此粘附素介导的结合是分化、定植、生物膜形成和病原体入侵的前奏。这些事件反过来导致发病率和死亡率的并发症，在免疫功能低下和慢性疾病患者中尤其常见。白色念珠菌粘附素与发病机制和生物膜形成有关。它们与哺乳动物组织结合，引起真菌细胞聚集，并与其他微生物病原体共同聚集，介导多微生物感染。粘连素在组织和留置装置中形成持久和耐药的生物膜也很重要。