Analysis calcium entry

Corelli F, Manetti F, Tafi A, Campiani G, Nacci V, Botta M. Diltiazem-like calcium entry blockers A hypothesis of the receptor-binding site based on a comparative molecular field analysis model. J Med Chem 1997 40 125-31. 

Channels associated with capacitative calcium ion entry have been characterized electrophysiologically. In leukocytes, the current associated with the depletion of intracellular Ca2+ stores is highly Ca2+-selective and, on the basis of noise analysis, is believed to involve minute single channels [16] (see Ch. 6). This is the calcium release-activated calcium current (ICrac)- In other cell types, currents with significantly different properties have been identified, including in some instances store-operated nonse-lective cation channels. These marked electrophysiological distinctions may be indicative of distinct channel types mediating capacitative calcium ion entry in different cell types. 

Selected entries from Methods in Enzymology [vol, page(s)] Chelation, 238, 74, 76, 297 buffers [for analysis of exocytosis, 221, 132 preparation, 219, 186 modulation of cytosolic buffering capacity with quin2, 221, 159] fluorescence assay, 240, 724-725, 740-742 fluorescence imaging, 225, 531 238, 303-304, 322-325, 334-335 free intracellular levels after bacterial invasion, 236, 482-489 free calcium in solutions for membrane fusion analysis, calculation and control, 221, 149 homeostasis mechanisms, 238, 80 hormonal elevation, 238, 79 inositol phosphate effect on release, 238, 207 determination of cytosolic levels [computer methods, 238, 73-75 with fura-2, 238, 73, 146 with indo-1, 238, 298, 316-317 with quin-2, 238, 297] hormone effects, 238, 79 ionomycin effects, 238, 79 membrane depolarization effects,... 

Selected entries from Methods in Enzymology [vol, page(s)] Analysis, software for, 207, 717 barrier models, 207, 818 closed and open time estimation, 207, 755 data acquisition, 207, 747 modal behavior analysis, 207, 757 multiple channel problem, 207, 756 single-channel [extraction of kinetic information, 207, 765 measurement in tissue slices, 207, 220] synaptic, resolution improvement in patch clamp recording, 207, 216 whole-cell recording in calcium channel, 207, 181 fluctuation analysis, 207, 192. 

The hope that promiscuity is predictable is also supported by the identification of systematic patterns of promiscuity. For example, lactonases, and in particular lactonases that favor hydrophobic lactones, show a consistent tendency to promiscuously catalyze the hydrolysis of phosphotriesters. This pattern has now been seen in lactonases from three different superfamilies PLLs (TIM-barrels from the amidohydrolase superfamily Table 1, entry 11) PONs, or serum paraoxonases (calcium-dependent six-bladded /3-propellers Table 1, entry 13) and AHA (a lactonase from the metallo-/3-lactamase superfamily Table 1, entry 12). That very different scaffolds and active-sites configurations share the same promiscuity pattern suggests that these reactions share a key feature, probably in the geometry of their transition states. This feature must be distinct, also because many of these lactonases do not hydrolyze esters that are much closer to lactones than phosphotriesters, and should thus be amenable to structural analysis and prediction. 

Twenty milliliter of EDTA solution (1 ml equivalent to 72 pLg calcium) were titrated using Calcein as the indicator of fluorescence end point. The titrant contained 400/xg calcium/ml and the entries in the table represent milliliters of this titrant added for automatic stop. Dade Reagents analysis was 100 4/xg/ml for Lab-trol, and 81.0 3.2/xg/mlfor Patho-trol. Procedure and instrumental parameters are given in the text. 

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