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STRUCTURE INVESTIGATIONS ON INTERFERON TAU

STRUCTURE INVESTIGATIONS ON INTERFERON TAU
干扰素 TAU 的结构研究
批准号:
6626731
负责人:
NEPALLI RAMA KRISHNA
金额:
$19.37万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-01-01 至 2004-12-31

项目摘要

项目成果

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中文摘要
翻译
描述:(逐字摘自申请人的摘要)目前的提案是 目的了解绵羊干扰素-tau(IFNtau)的结构生物学。 这种蛋白质是I型干扰素家族的最新成员,包括 IFNAlpha IFNbeta和IFNAlpha。它是一种20 kDa的抗白细胞蛋白 在绵羊胚胎中,最初称为绵羊滋养层蛋白-I。 然而,它与IFNpha和IFNbeta显示出同源性。像其他干扰素一样, 绵羊IFNtau显示出抗增殖和抗病毒活性 物种,包括人类。然而,与其他干扰素不同,它不会 即使在高浓度下也会对细胞产生毒性,并且不会诱导 动物模型的体重减轻和骨髓抑制。因此,IFNtau是 由于它在治疗癌症方面的临床潜力,人们对它非常感兴趣 如肾癌,毛细胞白血病,结肠肿瘤,肾脏肿瘤, 以及艾滋病毒、乙肝和丙型肝炎等病毒感染两个独立的假设 与溶液结构和缺乏细胞毒性相关的测试 在调查过程中。这项研究也有可能 提供有关IFNtau信号转导机制的基本知识 在受体水平上。包括克隆在内的许多实验方法 表达15N/13C均一标记的重组蛋白, 多维核磁共振,分子模拟,圆二色谱,抗病毒 活性分析、抗增殖活性和细胞周期分析,以及 将使用细胞毒性测量。
英文摘要
DESCRIPTION: (Verbatim from the Applicant's Abstract) The current proposal is aimed at understanding the structural biology of ovine interferon-tau (IFNtau). This protein is a recent addition to the type I interferon family that includes IFNalpha IFNbeta, and IFNalpha. It is a 20 kDa antileuteolitic protein produced in sheep conceptuses, and originally called ovine trophoblast protein-I. However, it shows homology to IFNalpha and IFNbeta. Like other interferons, ovine IFNtau exhibits antiproliferative and antiviral activities across several species, including humans. Unlike other interferons, however, it does not exhibit toxicity to cells even at high concentrations, and does not induce weight loss and bone marrow suppression in animal models. Thus IFNtau is of considerable interest because of its clinical potential in treating cancers such as renal carcinoma, hairy cell leukemia, colon tumors, and kidney tumors, and viral infections such as HIV and hepatitis B and C. Two separate hypotheses relating to the solution structure and lack of cytotoxicity will be tested during the course of this investigation. This study is also likely to contribute to basic knowledge on the mechanism of signal transduction by IFNtau at the level of receptor. A number of experimental methods that include cloning and expression of uniformly 15N/13C-labeled recombinant proteins, multidimensional NMR, molecular modeling, circular dichroism, antiviral activity assay, antiproliferative activity and cell cycle analyses, and cytoxicity measurements will be used.
期刊论文(6)
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科研奖励(0)
会议论文
Refinement of the conformation of UDP-galactose bound to galactosyltransferase using the STD NMR intensity-restrained CORCEMA optimization.
使用 STD NMR 强度限制 CORCEMA 优化对与半乳糖基转移酶结合的 UDP-半乳糖的构象进行细化。
DOI: 10.1021/ja048703u
发表时间: 2004
期刊: Journal of the American Chemical Society
影响因子: 15
作者: [Jayalakshmi,V, Biet,Thorsten, Peters,Thomas, Krishna,NRama]
通讯作者: Krishna,NRama
Heavy labeling of recombinant proteins.
重组蛋白的重标记。
DOI: 10.1007/978-1-59745-456-8_11
发表时间: 2007
期刊: Methods in molecular biology (Clifton, N.J.)
影响因子: --
作者: [Rodriguez,Eric]
通讯作者: Rodriguez,Eric
An economical method for (15)N/(13)C isotopic labeling of proteins expressed in Pichia pastoris.
一种对毕赤酵母中表达的蛋白质进行 (15)N/(13)C 同位素标记的经济方法。
DOI: 10.1093/oxfordjournals.jbchem.a002957
发表时间: 2001
期刊: Journal of biochemistry
影响因子: 2.7
作者: [Rodriguez,E, Krishna,NR]
通讯作者: Krishna,NR
C-Src Kinase-Calmodulin Interaction: A Therapeutic Target For Pancreatic Cancer
C-Src Kinase-Calmodulin Interaction: A Therapeutic Target For Pancreatic Cancer
HIV-1 Capsid Protein/Cyclophilin-A Complex : A Structural Study
HIV-1 Capsid Protein/Cyclophilin-A Complex : A Structural Study
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