PROTEIN DEGRADATION IN P FALCIPARUM

恶性疟原虫中的蛋白质降解

基本信息

  • 批准号:
    3566951
  • 负责人:
  • 金额:
    $ 10.83万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1984
  • 资助国家:
    美国
  • 起止时间:
    1984-07-01 至 1992-06-30
  • 项目状态:
    已结题

项目摘要

The goal of this research project is to elucidate the functions of parasite proteases in the growth and maturation of the malarial parasite Plasmodium falciparum. The goal is related to a long- range objective of developing new antimalarial drugs targeted at parasite proteases, especially proteases involved in parasite-host interactions. The specific aims of this project are 1) to characterize acid and neutral proteases and to determine their roles in the degradation of hemoglobin; 2) to determine there roles of ATP-dependent and ATP-independent non-lysosomal proteolysis in the development of P.falciparum; 3) to elucidate the site of action of chloroquine; 4) to determine the roles of proteases in merozoite-host interactions. The following hypotheses will be tested: 1. Digestion of host cytosol by malarial parasites involves acid proteases in the parasite's food vacuole but also involves non- lysosomal pathways for the degradation of hemoglobin. 2. Chloroquine interferes with the digestion of hemoglobin by diverting hemin from sequestration into malarial pigment. The actual inhibitor of parasite growth is free hemin which inhibits proteolysis. 3. Chloroquine resistance results from mutations which increase the efficiency of sequestration of hemin into malarial pigment. 4. Surface proteases of merozoite-stage parasites are active participants in the process of invasion of erythrocytes by P.falciparum. Parasite proteases will be purified by HPLC procedures and will be characterized Cytochemical and immunocytochemical studies of cellular proteases will be carried out. Proteases will be carried out. Proteases will be isolated from various morphological states of the intraerythrocytic parasite.
这个研究项目的目的是阐明的功能

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)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

DAVID L VANDER JAGT其他文献

DAVID L VANDER JAGT的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('DAVID L VANDER JAGT', 18)}}的其他基金

Oxidative Stress, VEGF and Retinopathy
氧化应激、VEGF 和视网膜病变
  • 批准号:
    6620288
  • 财政年份:
    2002
  • 资助金额:
    $ 10.83万
  • 项目类别:
Oxidative Stress, VEGF and Retinopathy
氧化应激、VEGF 和视网膜病变
  • 批准号:
    6745536
  • 财政年份:
    2002
  • 资助金额:
    $ 10.83万
  • 项目类别:
Oxidative Stress, VEGF and Retinopathy
氧化应激、VEGF 和视网膜病变
  • 批准号:
    6414754
  • 财政年份:
    2002
  • 资助金额:
    $ 10.83万
  • 项目类别:
HUMAN ALDOSE REDUCTASE AND DIABETIC COMPLICATIONS
人醛糖还原酶与糖尿病并发症
  • 批准号:
    3244584
  • 财政年份:
    1992
  • 资助金额:
    $ 10.83万
  • 项目类别:
HUMAN ALDOSE REDUCTASE AND DIABETIC COMPLICATIONS
人醛糖还原酶与糖尿病并发症
  • 批准号:
    3244585
  • 财政年份:
    1992
  • 资助金额:
    $ 10.83万
  • 项目类别:
HUMAN ALDOSE REDUCTASE AND DIABETIC COMPLICATIONS
人醛糖还原酶与糖尿病并发症
  • 批准号:
    2142867
  • 财政年份:
    1992
  • 资助金额:
    $ 10.83万
  • 项目类别:
PROTEIN DEGRADATION IN P. FALCIPARUM
恶性疟原虫中的蛋白质降解
  • 批准号:
    3131137
  • 财政年份:
    1984
  • 资助金额:
    $ 10.83万
  • 项目类别:
PROTEIN DEGRADATION IN P FALCIPARUM
恶性疟原虫中的蛋白质降解
  • 批准号:
    3131134
  • 财政年份:
    1984
  • 资助金额:
    $ 10.83万
  • 项目类别:
PROTEIN DEGRADATION IN P FALCIPARUM
恶性疟原虫中的蛋白质降解
  • 批准号:
    3565473
  • 财政年份:
    1984
  • 资助金额:
    $ 10.83万
  • 项目类别:
PROTEIN DEGRADATION IN P FALCIPARUM
恶性疟原虫中的蛋白质降解
  • 批准号:
    3444693
  • 财政年份:
    1984
  • 资助金额:
    $ 10.83万
  • 项目类别:

相似海外基金

Establishment of aminoacid transporter directed prostate cancer therapy based on the liquid biopsy
基于液体活检的氨基酸转运蛋白定向前列腺癌治疗的建立
  • 批准号:
    20K09555
  • 财政年份:
    2020
  • 资助金额:
    $ 10.83万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Destribution of vesicular aminoacid transporters during postnatal development in the trigeminal neurons
三叉神经元出生后发育过程中囊泡氨基酸转运蛋白的分布
  • 批准号:
    24592762
  • 财政年份:
    2012
  • 资助金额:
    $ 10.83万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Dopaminergic regulation by D-aminoacid oxidase, an enzyme implicated in schizophrenia
D-氨基酸氧化酶(一种与精神分裂症有关的酶)对多巴胺能的调节
  • 批准号:
    G0801352/1
  • 财政年份:
    2009
  • 资助金额:
    $ 10.83万
  • 项目类别:
    Research Grant
STUDIES ON BETA-AMINOACID OLIGOMERS
β-氨基酸低聚物的研究
  • 批准号:
    7598802
  • 财政年份:
    2007
  • 资助金额:
    $ 10.83万
  • 项目类别:
Diseases Of Aminoacid Transport: Genetic, Molecular and Biochemical Studies
氨基酸运输疾病:遗传、分子和生化研究
  • 批准号:
    nhmrc : 402730
  • 财政年份:
    2006
  • 资助金额:
    $ 10.83万
  • 项目类别:
    NHMRC Project Grants
AMINOACID RESIDUE INVOLVED IN METAL ION BINDING BY CLASS II METALLOTHIONEINS (78)
参与 II 类金属硫蛋白金属离子结合的氨基酸残基 (78)
  • 批准号:
    6656505
  • 财政年份:
    2002
  • 资助金额:
    $ 10.83万
  • 项目类别:
AMINOACID RESIDUE INVOLVED IN METAL ION BINDING BY CLASS II METALLOTHIONEINS (78)
参与 II 类金属硫蛋白金属离子结合的氨基酸残基 (78)
  • 批准号:
    6659279
  • 财政年份:
    2002
  • 资助金额:
    $ 10.83万
  • 项目类别:
L-Aminoacid oxidase, biochemical mechanisms and apoptose induction
L-氨基酸氧化酶、生化机制和细胞凋亡诱导
  • 批准号:
    5368381
  • 财政年份:
    2002
  • 资助金额:
    $ 10.83万
  • 项目类别:
    Research Grants
AMINOACID RESIDUE INVOLVED IN METAL ION BINDING BY CLASS II METALLOTHIONEINS (78)
参与 II 类金属硫蛋白金属离子结合的氨基酸残基 (78)
  • 批准号:
    6504097
  • 财政年份:
    2001
  • 资助金额:
    $ 10.83万
  • 项目类别:
AMINOACID RESIDUE INVOLVED IN METAL ION BINDING BY CLASS II METALLOTHIONEINS (78)
参与 II 类金属硫蛋白金属离子结合的氨基酸残基 (78)
  • 批准号:
    6502534
  • 财政年份:
    2001
  • 资助金额:
    $ 10.83万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了