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Cell membrane complex defined

These organelles are the sites of energy production of aerobic cells and contain the enzymes of the tricarboxylic acid cycle, the respiratory chain, and the fatty acid oxidation system. The mitochondrion is bounded by a pair of specialized membranes that define the separate mitochondrial compartments, the internal matrix space and an intermembrane space. Molecules of 10,000 daltons or less can penetrate the outer membrane, but most of these molecules cannot pass the selectively permeable inner membrane. By a series of infoldings, the internal membrane forms cristae in the matrix space. The components of the respiratory chain and the enzyme complex that makes ATP are embedded in the inner membrane as well as a number of transport proteins that make it selectively permeable to small molecules that are metabolized by the enzymes in the matrix space. Matrix enzymes include those of the tricarboxylic acid cycle, the fatty acid oxidation system, and others. [Pg.9]

Peden AA, Oorschot V, Hesser BA, Austin CD, Scheller RH, et al. 2004. Localization of the AP-3 adaptor complex defines a novel endosomal exit site for lysosomal membrane proteins. J Cell Biol 164 1065-1076. [Pg.234]

The structure of the ligand-receptor complex defines the orientation of the ligand vwth respect to the cell membrane. The total surface area buried in the TNF-P-( TNFR)3 complex (1.120 A2) is about the same size as that in the hGH—(hGHbp)2 complex. Although the quaternary structures of fi ee and liganded TNF-P receptor are different, the structure and conformation of firee and bound ligand, TNF-P, are, like free and bound hGH, virtually identical, as shown by Naismith et cdP... [Pg.28]

Viruses can be defined as infectious particles that consist of a nucleic acid molecule surrounded by a protective coat made up of protein (Voet and Voet, 1995, pp. 841, 1074). The virus particle is known as a virion the protein coating is called a capsid, hi more complex viruses, the capsid may be encased by an envelope derived from a host cell membrane. [Pg.75]

A FIGURE 18-1 Overview of synthesis of major membrane lipids and their movement into and out of cells. Membrane lipids (e.g., phospholipids, cholesterol) are synthesized through complex multienzyme pathways that begin with sets of water-soluble enzymes and intermediates in the cytosol (D) that are then converted by membrane-associated enzymes into water-insoluble products embedded in the membrane (B), usually at the interface between the cytosolic leaflet of the endoplasmic reticulum (ER) and the cytosol. Membrane lipids can move from the ER to other organelles (H), such as the Golgi apparatus or the mitochondrion, by either vesicle-mediated or other poorly defined mechanisms. Lipids can move into or out of cells by plasma-membrane transport proteins or by lipoproteins. Transport proteins similar to those described in Chapter 7 that move lipids (0) include sodium-coupled symporters that mediate import CD36 and SR-BI superfamily proteins that can mediate... [Pg.744]

There are two actions that create intracellular molecules produce intracellular molecule complex for freely diffusing and membrane attached strictly intracellular molecule complexes and display membrane molecule complex for trans-membrane complexes or receptors that are on the outer leaflet of the cytoplasmic membrane. After clicking add action make sure the new action is highlighted. Then click on the action part of the header bar and select the appropriate action. Drag and drop the complex from the list of defined complexes and select location and amount ( rrNote 9). After having defined all actions needed to initialize the cellular biochemistry assign a name to the mechanism and click add mechanism to cell type. ... [Pg.516]


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