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Characterization of PTMs on Env to support HIV vaccine development

Env 上 PTM 的表征以支持 HIV 疫苗的开发

基本信息

批准号：
8890080
负责人：
HEATHER R DESAIRE
金额：
$ 36.46万
依托单位：
UNIVERSITY OF KANSAS LAWRENCE
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-08-01 至 2017-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8890080
关键词：
Academic Medical Centers Affect Antibodies Antigens Area Binding Biological Biological Response Modifier Therapy CH01 Cell Line Collaborations Communities Data Data Analyses Development Disulfides Glycopeptides Glycoproteins Goals HIV HIV envelope protein HIV vaccine HIV-1 Health Heterogeneity High Pressure Liquid Chromatography Human Lead Left Link Maps Methods Modeling Modification Molecular Molecular Conformation Monitor Peptides Performance Pharmacologic Substance Polysaccharides Post-Translational Protein Processing Preparation Problem Solving Protein Analysis Protein Binding Proteins Protocols documentation Recombinant Antibody Recombinant Proteins Recombinants Research Personnel Sampling Site Techniques Technology Transfection Universities Vaccine Design Vaccines Validation Virus Work base computerized data processing data acquisition disulfide bond env Gene Products experience glycosylation immunogenicity innovation insight medical schools novel strategies protein structure function research study therapeutic protein tool vaccine candidate vaccine development vaccine efficacy

项目摘要

DESCRIPTION (provided by applicant): The ultimate goal of this proposal is to develop broadly applicable methods to analyze glycosylation and disulfide bonding of glycoproteins and to apply those methods to the HIV Envelope protein (Env). This work would be accomplished by completing four specific aims: (1) Develop a new glycoproteomic method, where glycosylation site occupancy is quantified and glycoform heterogeneity is simultaneously characterized, all in one experiment. (2) Profile Env glycosylation site occupancy and glycopeptide heterogeneity to answer several important biological questions. (3) Develop an automated analysis protocol for identifying disulfide- linked peptides. (4) Characterize the disulfide bonding of Env to answer several important biological questions. The bulk of the work would be completed by combining expertise in biological sample handling, HPLC, and mass spectral (MS) data acquisition and analysis to develop the necessary tools. The utility of all the tools would be demonstrated by incorporating them to solve problems relevant to HIV vaccine development. Of particular note are studies in Aim 2, where the tools are used to correlate changes in glycan content with changes in vaccine efficacy. This work can broadly impact human health by providing fundamental insights into how post-translational modifications impact HIV vaccine candidates' efficacy. Likewise, methods for glycoprotein and disulfide analysis are enabling bioanalytical technologies that can be used in a variety of venues, from protein structure/function analyses to pharmaceutical development. The application work related to HIV proteins is done in collaboration with Dr. Barton F. Haynes at Duke University Medical Center and Dr. Bing Chen at Harvard University Medical School.

描述（由申请方提供）：本提案的最终目标是开发广泛适用的方法来分析糖蛋白的糖基化和二硫键，并将这些方法应用于HIV包膜蛋白（Env）。这项工作将通过完成四个具体目标来完成：（1）开发一种新的糖蛋白质组学方法，其中糖基化位点占用定量和糖型异质性同时表征，所有这些都在一个实验中进行。(2)分析Env糖基化位点占有率和糖肽异质性，以回答几个重要的生物学问题。(3)开发用于识别二硫键连接肽的自动化分析方案。(4)表征Env的二硫键以回答几个重要的生物学问题。大部分工作将通过结合生物样品处理、HPLC和质谱（MS）数据采集和分析方面的专业知识来完成，以开发必要的工具。所有这些工具的效用将通过将其纳入解决与艾滋病毒疫苗开发有关的问题来证明。特别值得注意的是目标2中的研究，其中工具用于将聚糖含量的变化与疫苗效力的变化相关联。这项工作可以通过提供关于翻译后修饰如何影响HIV候选疫苗功效的基本见解来广泛影响人类健康。同样，糖蛋白和二硫键分析方法使生物分析技术能够用于各种场合，从蛋白质结构/功能分析到药物开发。与HIV蛋白相关的应用工作是与巴顿F.杜克大学医学中心的海恩斯和哈佛大学医学院的陈兵博士。