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81.
Acknowledgment of priority 相似文献
82.
The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex 总被引:8,自引:0,他引:8
The bacteriocidal capacity of phagocytic cells is impaired in X-linked chronic granulomatous disease (X-CGD), a disorder characterized by the absence of functional plasma-membrane-associated NADPH oxidase. The components of this oxidase system, their correspondence with specific genetic loci, and the primary protein defect in X-CGD remain incompletely defined. We recently reported cloning of the putative X-CGD gene on the basis of DNA linkage. To identify the predicted protein in vivo, antibodies were raised to a synthetic peptide derived from the complementary DNA sequence and to a fusion protein produced in Escherichia coli. In Western blots antisera detect a neutrophil protein of relative molecular mass in 90,000 (90K) that is absent in X-CGD patients. Antisera also react with the larger component of cytochrome b recently purified from neutrophil plasma membranes as a complex of glycosylated 90K and non-glycosylated 22K polypeptides. Based on our identification of the X-CGD protein in vivo, we propose that one of its critical roles is to interact with the 22K species to form a functional cytochrome b complex. 相似文献
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84.
Insulin-regulatable tissues express a unique insulin-sensitive glucose transport protein 总被引:43,自引:0,他引:43
At least three different glucose transport systems exist in mammalian cells. These are: (1) the constitutively active, facilitative carrier characteristic of human erythrocytes, Hep G2 (ref. 2) cells and rat brain; (2) the Na-dependent active transporter of kidney and small intestine; and (3) the facilitative carrier of rat liver (B. Thorens and H. F. Lodish, personal communication). A fourth possible glucose transport system is the insulin-dependent carrier that may be specific to muscle and adipose tissue. This transporter resides primarily in an intracellular compartment in resting cells from where it translocates to the cell surface upon cellular insulin exposure. This raises the question of whether hormonal regulation of glucose transport is conferred by virtue of a tissue-specific signalling mechanism or a tissue-specific glucose transporter. Here we present data supporting the latter concept based upon a monoclonal antibody against the fat cell glucose transporter that identifies a unique, insulin-regulatable glucose transport protein in muscle and adipose tissue. 相似文献
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Protein covalently linked to foot-and-mouth disease virus RNA. 总被引:44,自引:0,他引:44
89.
Dora R. M. Passino G. W. Brown Jr. 《Cellular and molecular life sciences : CMLS》1976,32(11):1376-1377
Summary Allantoinase, an enzyme in the purine-urea cycle, was found inEudistylia vancouveri (Polychaeta). The enzyme had a pH optimum at 7.6 TheK
m
was 0.012M allantoin, and the Arrhenius energy of activation was 12.6 to 14.6 kcal/mol.Supported by the U. S. National Science Foundation (Institutional Grant) and by the U. S. Environmental Protection Agency Grant No. T-900204 (WP-175). Publication No. 10 of the Laboratory of Biochemical Ecology; College of Fisheries Contribution No. 458. We thank Dr.Robert L. Fernald for generously making available to us the facilities of the Friday Harbor Laboratories, Friday Harbor, Washington. 相似文献
90.