MOLECULAR BASIS OF ANTIGENIC SPECIFICITY
抗原特异性的分子基础
基本信息
- 批准号:3445762
- 负责人:
- 金额:$ 4.66万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1986
- 资助国家:美国
- 起止时间:1986-06-01 至 1989-05-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Preliminary thermodynamic studies of a high affinity monoclonal
anti-fluorescyl antibody (4-4-20) indicate that its active site is a
shallow hydrophobic pocket, which binds fluorescein primarily through
entropy. Moreover, high resolution diffraction data (2.5 Angstrom) is
available for the liganded antigen binding fragment (Fab) of this antibody,
which crystallizes in 16% polyethyleneglycol. Liganded Fab fragments also
crystallize in a less polar solvent system (46.7%
2-methyl-2,4-pentanediol). The affinity of the intact IgG molecule is
300-fold lower in this solvent. Correlated crystal and solution studies of
both crystal systems are planned. With this information we hope to explain
the molecular basis of antigen binding to this antibody. Crystallization
trials are currently in progress with four other monoclonal anti-fluorescyl
antibodies which are idiotypically related to 4-4-20, but exhibit
affinities which vary over a 1000-fold range. Solution studies are planned
to determine whether the entropy predominance and active site
characteristics of 4-4-20 are common to the other clones as well.
Idiotypic determinants are generally thought to be located at or near the
active site. Crystal studies should clarify the nature of idiotypic
determinants and whether idiotypic reagents are valid tools for identifying
related active sites.
High resolution diffraction data (2.0 Angstrom) is available for the
unliganded Fab fragment of a monoclonal antibody which binds single
stranded DNA (BV04-01). In solution, the protein exhibited a base
specificity for pyrimidines, with greater affinity for thymine than
uracil. This antibody is of clinical importance because it was isolated
from a mouse with an autoimmune syndrome similar to systemic lupus
erythematosus. We have obtained a low-resolution (6 Angstrom) structure
and plan to extend this solution to higher resolution. We also plan to
perfuse oligonucleotides into crystals to determine the molecular basis of
the observed pyrimidine specificity.
高亲和力单克隆抗体的初步热力学研究
抗荧光抗体(4-4-20)表明其活性位点是一个
浅疏水口袋,主要通过
熵 此外,高分辨率衍射数据(2.5埃)是
可用于该抗体的配体化抗原结合片段(Fab),
其在16%聚乙二醇中结晶。 配体Fab片段还
在极性较小的溶剂体系中结晶(46.7%),
2-甲基-2,4-戊二醇)。 完整IgG分子的亲和力为
300-在这种溶剂中会降低一倍 相关晶体和溶液研究
两个水晶系统都在计划中。 我们希望通过这些信息来解释
抗原与抗体结合的分子基础 结晶
目前正在进行其他四种单克隆抗荧光素抗体的试验。
与4-4-20独特相关的抗体,但表现出
其亲和力在1000倍范围内变化。 计划进行解决方案研究
来确定熵优势和活性位点
4-4-20的特征对于其它克隆也是共同的。
独特型决定因素通常被认为位于或接近
活性部位 晶体研究应阐明独特型的性质
决定因素和独特型试剂是否是有效的工具,
相关的活跃网站
高分辨率衍射数据(2.0埃)可用于
单克隆抗体的未配体Fab片段,其结合单个
链DNA(BV 04 -01)。 在溶液中,该蛋白质显示出一种碱,
对嘧啶的特异性,对胸腺嘧啶的亲和力大于
尿嘧啶。 这种抗体具有临床重要性,因为它是分离出来的,
来自一只患有类似系统性狼疮的自身免疫综合征的老鼠
红斑 我们已经获得了低分辨率(6埃)结构
并计划将该解决方案扩展到更高的分辨率。 我们还计划
将寡核苷酸灌注到晶体中以确定
观察到的嘧啶特异性。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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James N Herron其他文献
James N Herron的其他文献
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{{ truncateString('James N Herron', 18)}}的其他基金
Novel Reagents and Methods for Rapid and High Throughput Detection of Aflatoxin C
快速高通量检测黄曲霉毒素C的新试剂和方法
- 批准号:
8396243 - 财政年份:2013
- 资助金额:
$ 4.66万 - 项目类别:
Novel Reagents and Methods for Rapid and High Throughput Detection of Aflatoxin C
快速高通量检测黄曲霉毒素C的新试剂和方法
- 批准号:
8739645 - 财政年份:2013
- 资助金额:
$ 4.66万 - 项目类别:
Novel Method and Self Contained System for Reliable Assessment of Potency of Botu
可靠评估博土功效的新方法和独立系统
- 批准号:
8126652 - 财政年份:2011
- 资助金额:
$ 4.66万 - 项目类别:
Novel Method and Self Contained System for Reliable Assessment of Potency of Botu
可靠评估博土功效的新方法和独立系统
- 批准号:
8337736 - 财政年份:2011
- 资助金额:
$ 4.66万 - 项目类别:
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