PEPTIDES IDENTIFIED FROM THE TYPE I DIABETES ASSOCIATED MHC CLASS I-H2-KD
从 I 型糖尿病相关 MHC I-H2-KD 类中鉴定出的肽
基本信息
- 批准号:8168690
- 负责人:
- 金额:$ 0.85万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-03-10 至 2010-12-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAffinityAmino AcidsAreaAutoantigensAutoimmune DiabetesBindingBiologicalCancer VaccinesComplexComputer Retrieval of Information on Scientific Projects DatabaseDiseaseDissociationEpitopesFundingGrantHistocompatibility Antigens Class IIImmune responseInstitutionInsulin-Dependent Diabetes MellitusInvestigationLengthLifeMajor Histocompatibility ComplexNatureOutcomePeptidesPlayProcessResearchResearch PersonnelResourcesRoleSourceSpecificitySynthetic Peptide LibrariesUnited States National Institutes of HealthViralbaseimprovedpathogenresearch studyresponsetumor immunology
项目摘要
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 repertoire of peptides bound by major histocompatability complexes (MHC) determines the fate of important biological outcomes such as the cellular defense and immune responses to foreign invaders or in some aberrant cases reactivity to self antigens. Detailed analyses of naturally processed peptides from class I and II MHC molecules have revealed certain general features, for example the lengths of naturally processed peptides selected by class I MHC molecules are usually restricted to 8-10-mers whereas those selected by class II MHC molecules are longer and more variable, usually between 14-24-mer. More importantly, detailed analyses of naturally processed peptides have addressed key issues regarding the specificity of peptide-selection among closely related MHC molecules, which was not evident in prior studies involving synthetic peptide libraries.
In this analyses, we sought to identify the nature and motif of peptides that are selected by the class I MHC molecule, H-2Kd. We selected H-2Kd because it may play a significant role in several areas of disease including: responses against viral and bacterial pathogens, autoimmune diabetes, tumor immunology, and the efficacy of peptide-based tumor vaccines. Results from our analyses of large numbers of peptides selected by H-2Kd have firmly established the peptide-binding motif. Although a large fraction of naturally selected peptides were 8 to 10 amino acids in length, there were a significant fraction that were of longer length, some as long as 18-mers. Binding studies demonstrated that while the short peptides bound with higher affinity and formed long-lived peptide-MHC complexes, the longer peptides bound weakly and had a fast dissociation rate. Trimming the long peptides did not improve binding interactions and conversely extending the 9-mer naturally processed epitopes did not decrease binding. Finally, the mode of binding of the longer peptides was investigated. Results from these experiments demonstrate that the Naturally processed peptides selected by H-2Kd varied in length from 8-mers to 18-mers ? although most peptides were 8-10 amino acids, there was a significant fraction that were 10 amino acids in length. The immunological significance of these peptides is currently under investigation.
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。
由主要组织相容性复合物(MHC)结合的肽库决定重要生物学结果的命运,例如对外来入侵者的细胞防御和免疫反应或在某些异常情况下对自身抗原的反应性。 对来自I类和II类MHC分子的天然加工肽的详细分析揭示了某些一般特征,例如由I类MHC分子选择的天然加工肽的长度通常限于8-10聚体,而由II类MHC分子选择的天然加工肽的长度更长且更可变,通常在14-24聚体之间。 更重要的是,对天然加工肽的详细分析已经解决了关于在密切相关的MHC分子中肽选择的特异性的关键问题,这在涉及合成肽文库的先前研究中并不明显。
在该分析中,我们试图鉴定由I类MHC分子H-2Kd选择的肽的性质和基序。我们选择H-2Kd是因为它可能在几个疾病领域发挥重要作用,包括:对病毒和细菌病原体的反应,自身免疫性糖尿病,肿瘤免疫学和基于肽的肿瘤疫苗的功效。 从我们的分析结果的大量的肽选择H-2Kd已经牢固地建立了肽结合基序。虽然大部分天然选择的肽的长度为8至10个氨基酸,但也有相当一部分长度较长,有些长达18聚体。 结合研究表明,虽然短肽结合具有较高的亲和力,并形成长寿命的肽-MHC复合物,较长的肽结合弱,并有一个快速的解离速率。修剪长肽没有改善结合相互作用,相反地,延伸9聚体天然加工的表位没有降低结合。最后,研究了较长肽的结合模式。从这些实验的结果表明,自然加工的肽选择的H-2Kd不同的长度从8聚体到18聚体?尽管大多数肽是8-10个氨基酸,但有相当一部分长度是10个氨基酸。 这些肽的免疫学意义目前正在研究中。
项目成果
期刊论文数量(0)
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{{ truncateString('EMIL Raphael UNANUE', 18)}}的其他基金
Identification of relevant peptides involved in the initiation and progression of autoimmune diabetes
鉴定参与自身免疫性糖尿病发生和进展的相关肽
- 批准号:
10246429 - 财政年份:2018
- 资助金额:
$ 0.85万 - 项目类别:
Identification of relevant peptides involved in the initiation and progression of autoimmune diabetes
鉴定参与自身免疫性糖尿病发生和进展的相关肽
- 批准号:
9689765 - 财政年份:2018
- 资助金额:
$ 0.85万 - 项目类别:
AUTOIMMUNE DIABETES: EARLY EVENTS IN ISLETS OF LANGERHANS
自身免疫性糖尿病:朗格汉斯岛的早期事件
- 批准号:
9197630 - 财政年份:2015
- 资助金额:
$ 0.85万 - 项目类别:
CHARACTERIZATION OF ANTIGENIC PEPTIDES PRESENTED BY I-AG7
I-AG7 呈现的抗原肽的表征
- 批准号:
8361393 - 财政年份:2011
- 资助金额:
$ 0.85万 - 项目类别:
IDENTIFICATION OF MODIFIED AND NATURAL HEL PEPTIDE FRAGMENTS PRESENTED BY MHC
MHC 呈现的修饰和天然 HEL 肽片段的鉴定
- 批准号:
8361330 - 财政年份:2011
- 资助金额:
$ 0.85万 - 项目类别:
IDENTIFICATION OF MODIFIED AND NATURAL HEL PEPTIDE FRAGMENTS PRESENTED BY MHC
MHC 呈现的修饰和天然 HEL 肽片段的鉴定
- 批准号:
8168678 - 财政年份:2010
- 资助金额:
$ 0.85万 - 项目类别:
CHARACTERIZATION OF ANTIGENIC PEPTIDES PRESENTED BY I-AG7
I-AG7 呈现的抗原肽的表征
- 批准号:
8168793 - 财政年份:2010
- 资助金额:
$ 0.85万 - 项目类别:
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