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
- 来源:
- 关键词:Plasmodium falciparum aminoacid antibody formation antimalarial agents drug design /synthesis /production enzyme linked immunosorbent assay enzyme structure growth /development hemoglobin high performance liquid chromatography host organism interaction human tissue immunochemistry lysosomes monoclonal antibody peptidases proteolysis
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)
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{{ truncateString('DAVID L VANDER JAGT', 18)}}的其他基金
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:
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