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Recombinant 47-kilodalton cytosol factor restores NADPH oxidase in chronic granulomatous disease.

作者信息

Lomax K J, Leto T L, Nunoi H, Gallin J I, Malech H L

机构信息

Bacterial Diseases Section, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

出版信息

Science. 1989 Jul 28;245(4916):409-12. doi: 10.1126/science.2547247.

DOI:10.1126/science.2547247
PMID:2547247
Abstract

A 47-kilodalton neutrophil cytosol factor (NCF-47k), required for activation of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase superoxide (O2-.) production, is absent in most patients with autosomal recessive chronic granulomatous disease (AR-CGD). NCF-47k cDNAs were cloned from an expression library. The largest clone predicted a 41.9-kD protein that contained an arginine and serine-rich COOH-terminal domain with potential protein kinase C phosphorylation sites. A 33-amino acid segment of NCF-47k shared 49% identity with ras p21 guanosine triphosphatase activating protein. Recombinant NCF-47k restored O2-. -producing activity to AR-CGD neutrophil cytosol in a cell-free assay. Production of active recombinant NCF-47k will enable functional regions of this molecule to be mapped.

摘要

相似文献

1
Recombinant 47-kilodalton cytosol factor restores NADPH oxidase in chronic granulomatous disease.
Science. 1989 Jul 28;245(4916):409-12. doi: 10.1126/science.2547247.
2
[Molecular bases of chronic granulomatous disease--analysis of the involvement of cytosol factors for NADPH oxidase].
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Two cytosolic neutrophil oxidase components absent in autosomal chronic granulomatous disease.常染色体慢性肉芽肿病中不存在的两种胞质嗜中性粒细胞氧化酶成分。
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Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.中性粒细胞p22-吞噬细胞色素b亚基胞质结构域中的点突变与无功能的NADPH氧化酶及慢性肉芽肿病相关。
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Chronic granulomatous disease due to a defect in the cytosolic factor required for nicotinamide adenine dinucleotide phosphate oxidase activation.由于烟酰胺腺嘌呤二核苷酸磷酸氧化酶激活所需的胞质因子缺陷导致的慢性肉芽肿病。
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