Subcellular

Plattner H 1989 Electron Microscopy of Subcellular Dynamics (London CRC)... 

Knoll G and Plattner H 1989 Ultrastructural analysis of biological membrane fusion and a tentative correlation with biochemical and biophysical aspects Electron Microscopy of Subcellular Dynamics ed H Plattner (London CRC) pp 95-117... 

Eukaryote Organism whose cells have a discrete nucleus and other subcellular compartments (cf. prokaryote)... 

W. W. Douglas, J. Nagasawa, and R. Schulz in H. Heller and K. Lederis, eds., Subcellular Organisation andFunction in Endocrine Tissues, University Press, Cambridge, Mass., 1971, pp. 353—377. 

The next steps of glucose catabolism are called the citric acid cycle. The pyruvic acid formed in glycolysis is transported into the mitochondria, which arc subcellular organelles with double (inner and outer) membranes. They are referred to as the powerhous-... 

Dose-response curves depict the response to an agonist in a cellular or subcellular system as a function of the agonist concentration. Specifically, they plot response as a function of the logarithm of the concentration. They can be defined completely by three parameters namely, location along the concentration axis, slope, and maximal asymptote... 

DeSa, R., Hastings, J. W., and Vatter, A. E. (1963). Luminescent crystalline particles an organized subcellular bioluminescent system. Science 141 1269-1270. 

Rizzuto, R., Marisa, B., Pizzo, P., Murgia, M., and Pozzan, T. (1995). Chimeric green fluorescent protein as a tool for visualizing subcellular organelles in living cells. Curr. Biol. 5 635-642. 

Some members of the Liliaceae accumulate free azetidine-2-carboxylic acid in a much higher concentration than that found to be lethal to mung bean seedlings, but it is not incorporated into their proteins. Fowden (43) postulated that these plants either had a proline-incorporating system which was more specific than that found in other species, or some subcellular mechanism operated to prevent the homolog from reaching the sites involved in protein synthesis. Data which supported the first suggestion were subsequently obtained (116). 

In addition to effects on biochemical reactions, the inhibitors may influence the permeability of the various cellular membranes and through physical and chemical effects may alter the structure of other subcellular structures such as proteins, nucleic acid, and spindle fibers. Unfortunately, few definite examples can be listed. The action of colchicine and podophyllin in interfering with cell division is well known. The effect of various lactones (coumarin, parasorbic acid, and protoanemonin) on mitotic activity was discussed above. Disturbances to cytoplasmic and vacuolar structure, and the morphology of mitochondria imposed by protoanemonin, were also mentioned. Interference with protein configuration and loss of biological activity was attributed to incorporation of azetidine-2-carboxylic acid into mung bean protein in place of proline. 

AKAPs are cyclic AMP-dependent protein kinase (PKA)-anchoring proteins, a family of about 30 proteins anchoring PKA at subcellular sites in close vicinity to a certain substrate. 

Bile acid synthesis from cholesterol is the prime pathway for cholesterol catabolism. Cholesterol is converted into bile acids via multiple pathways which involve 17 different enzymes. Many of these enzymes are predominantly expressed in the liver and are localized in several different subcellular... 

Subcellular localization pH Optimum Amino acids (in human) Species... 

The ECE isoforms show different subcellular distributions and enzymatic characteristics (Table 2). ECE-la and ECE-lc are mainly expressed at the cell surface, whereas ECE-lb, ECE-Id and ECE-2 are expressed intracellularly. Plasma membrane-bound ECE cleaves big-ET-1 circulating in the blood, whereas intracellular ECE isoforms are involved in the generation of mature endothelins. In addition, ECEs (as well as NEP and the insulin-degrading enzyme) contribute to the degradation of amyloid (3 (A 3) peptide. 

GPCR function has been shown to be regulated by several different mechanisms. The number of receptors on the plasma membrane may be regulated by transcription, mRNA stability, biosynthetic processing, and protein stability. In addition, the function of receptors in the plasma membrane can be influenced by regulatory phosphorylation and by association with other proteins that determine the subcellular location of receptors relative to other signaling molecules. 

In the nervous system, DAT, NET, and SERT are distributed along axons, soma and dendrites. On the subcellular level they are localized at the... 

Protein trafficking is the transport of proteins to their correct subcellular compartments or to the extracellular space ( secretory pathway ). Endo- and exocytosis describe vesicle budding and fusion at the plasma membrane and are by most authors not included in the term protein trafficking. Protein quality control comprize all cellular mechanisms, monitoring protein folding and detecting aberrant forms. 

On the molecular level, all TAARs for which ligands are available, couple to Gas, at least in recombinant systems. Links to other signaling pathways as well as potential heterodimerization within the TAAR family or with other GPCRs have so far not been observed. All TAAR genes have a very similar size of about 1 kb, and posttranslational modification and subcellular trafficking of the receptors are both not well understood. 

Trafficking is controlled movement of a protein from one subcellular location to another. 

SARA is a scaffolding protein that regulates the subcellular localization of inactivated R-Smads, potentially scaffolding the TGF-P receptor kinase to the Smad 2 substrate. Filamins are a family of actin polymerization proteins that also form scaffolds for a range of signaling proteins including SAP kinases such as MKK-4, small GTPases Rho and Ras, as well as Smad 2 and Smad 5. 

ELF, a (3-Spectrin, is a key component of TGF- 3 signaling that functions to recruit Smads to the receptor by controlling the subcellular localization of Smad 3 and Smad 4. Interestingly, ELF does not appear to interact with SARA or filamin, and in elf mutants, SARA and filamin distribution is the same as in wild-type mice. Thus, TGF- 3 signaling through R-Smad/ ELF interactions may work by way of a different mechanism than that of SARA and filamin. 

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