Sortase A anchoring mechanism

分选酶A锚定机制

• 批准号: 7257122
• 负责人: DEBORAH LEON-ROSSELL
• 金额: $ 2.92万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-07-15 至 2008-07-14
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7257122
• 关键词: Active Sites; Amino Acid Substitution; Amino Acids; Animals; Anti-Infective Agents; Antibiotics; Back; Bacteria; Bacterial Adhesion; Bacterial Infections; Binding; Biological Assay; Catalysis; Cell Wall; Complex; Cysteine Protease; Effectiveness; Enzymes; Fellowship; Fluorescence; Gram-Positive Bacteria; Immune response; Immune system; Individual; Infection; Kinetics; Knowledge; Lead; Mediating; Membrane; Membrane Proteins; Microbe; Mutate; Mutation; NMR Spectroscopy; Organ; Organism; Peptides; Peptidoglycan; Peptidyltransferase; Personal Satisfaction; Play; Property; Proteins; Reaction; Research; Resistance; Role; Series; Signal Transduction; Solutions; Sorting - Cell Movement; Staphylococcus aureus; Structure; Testing; Tissues; Work; base; design; in vivo; inhibitor/antagonist; pathogenic bacteria; prevent; sortase; transpeptidation

DESCRIPTION (provided by applicant): Gram-positive bacteria adhere to specific tissues in animals using the surface proteins displayed on their cell wall. These surface proteins promote bacterial adhesion, evasion of the host immune system and invasion of the host organism. The enzymes responsible for attaching these proteins to the cell wall are called sortases and they are found in all gram-positive bacteria. The focus of this proposal is to study sortase A (SrtA) from Staphylococcus aureus. To obtain a better understanding of the universal anchoring mechanism of sortases we will design and test the enzymatic effectiveness of several inhibitors of SrtA. We also propose to elucidate the structure of the SrtA-inhibitor complex by using NMR spectroscopy. We will identify the amino acids that are important for catalysis and substrate binding by introducing single amino acid mutations in SrtA. The knowledge gained from this study will hopefully lead to ways of disabling this anchoring mechanism and thereby preventing bacterial infection. Work leading to the creation of anti-infective agents against pathogenic bacteria should be prioritized especially in an era where bacteria have developed a resistance to many commonly used antibiotics.

描述（由申请人提供）：革兰氏阳性细菌通过细胞壁上的表面蛋白附着在动物的特定组织上。这些表面蛋白促进细菌粘附，逃避宿主免疫系统和入侵宿主生物。负责将这些蛋白质附着在细胞壁上的酶被称为分选酶，它们存在于所有革兰氏阳性细菌中。本课题的重点是研究金黄色葡萄球菌的分选酶A （SrtA）。为了更好地理解排序酶的普遍锚定机制，我们将设计和测试几种SrtA抑制剂的酶效。我们还建议利用核磁共振光谱来阐明srta抑制剂配合物的结构。我们将通过在SrtA中引入单氨基酸突变来确定对催化和底物结合重要的氨基酸。从这项研究中获得的知识有望导致禁用这种锚定机制的方法，从而防止细菌感染。应该优先考虑开发针对致病菌的抗感染药物，特别是在细菌对许多常用抗生素产生耐药性的时代。

项目成果

Identification of the major expressed S-layer and cell surface-layer-related proteins in the model methanogenic archaea: Methanosarcina barkeri Fusaro and Methanosarcina acetivorans C2A.

• DOI: 10.1155/2012/873589
• 发表时间: 2012
• 期刊: Archaea (Vancouver, B.C.)
• 作者: Rohlin L;Leon DR;Kim U;Loo JA;Ogorzalek Loo RR;Gunsalus RP
• 通讯作者: Gunsalus RP