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Complexes matrix-bound

MERR1FIELD. R. BRUCE (I92I-). An American ehemisi who won (he Nobel prize for chemistry in 1984 Merrilield was cited lor work on the use of solid matrix as an aid to chemical synthesis of complex pepiides and proteins Mis synthesis leehniques have been used in Ihe development of solid matrix-bound inorganic and organic agents. Awarded doctorate from l. C.l. A... [Pg.981]

Immunocapture-polymerase chain reaction (IC-PCR) is a synthesis of two commonly used diagnostic tools. This method exploits the high-affinity binding of antibodies to provide a facile method of purification, usually from a complex matrix, supplying the substrate for PCR detection. PCR exponentially amplifies a deoxyribonucleic acid (DNA) template in a temperature-dependent fashion by the annealing of oligonucleotide primers, enzymatic extension of bound primers by a heat-stable polymerase, followed by denaturation of... [Pg.308]

Use of test samples containing naturally incurred substances has the advantage of testing the ability of study participants to extract complexed or bound contaminants. However, the concentrations of naturally incurred substances in the sample matrix cannot usually be known to the same level of accuracy as spiked substances. One compromise that is sometimes useful is to prepare test samples by spiking, but to age the samples before dispatch to allow time for the added substances to interact with the matrix and therefore better simulate real world situations. [Pg.115]

Wine is a very complex matrix and the accurate, selective determination of species constitutes a challenge for analytical chemists. Furthermore, the speciation analysis of metals bound to biological ligands is a subject of increasing interest since complexation may reduce their toxicity and bioavailability. There is a limited number of studies concerning the speciation analysis of metals or metalloids in wines. Arsenite, arsenate, MMA, and DMA were separated in less than 10 min by means of an anion-exchange column [88], Arsenic species detection was accomplished by the direct coupling of the column effluent to an HG system and AFS was used for detection. LoDs in white wine were 0.16, 0.33, 0.32, and 0.57 ng ml-1 for As(III), DMA, MMA, and As(V), respectively. In real samples... [Pg.474]

Polymers can also be used for the physical immobilization of metal complexes. For example, the degree of swelling observed for 1% crosslinked polystyrene varies with solvents more swelling is observed in THF than in methanol. Thus, the cationic complex [(diphos)Rh(NBD)]PF6 can be adsorbed onto polystyrene in THF. When dried and extracted with methanol, the complex is bound within the polystyrene matrix. The immobilized complex is a catalyst for the hydrogenation of 1-hexene in methanol. ... [Pg.4723]

Ru-porphyrin complexes covalently bound to MCM-41 were used as catalysts for the oxidation of alkenes, giving turnover numbers 20-40 times higher than the free complex [190]. Porphyrin complexes have also been attached to Nb dopants in the MCM-41 matrix, and behaved as cyclohexene epoxidation catalysts and were stable towards ligand degradation [44b]. Grafting of ethylenediamine ligands on... [Pg.2840]

This separation technique is widely used in the separation of specific proteins and biological molecules. But it has had much less use on environmental samples until recently with work on small molecules, such as atrazine (Thomas et al., 1994). The advantage of this technique is that it is highly specific for the compounds of interest or class of compounds, which may be bound from a complex matrix that would be difficult to assay directly. [Pg.319]

The cytochrome system represents the final common path of oxidation and coupled phosphorylation in the eukaryotic cell. The components of this system [1-3] encompass the crystallizable cytochromes c, which have yielded much information to the protein chemist, as well as the matrix-bound cytochromes b, Ci, and a, which have revealed themselves largely to the spectroscopist. The cytochromes can react with one another and can undergo reversible changes in the proteins themselves [3]. In this sense, they resemble the subunits of a protein more than they do independent individuals, forming a constellation of apoproteins each with its characteristic heme prosthetic group. The complete system appears only in the mitochondrion, where the vectorial reactions in which the cytochromes participate are regulated in concert by phosphate acceptor. Induction and repression similarly involve not only particular cytochromes but the entire complex. This, in turn, is one aspect of the regulation of metalloporphyrins which is coordinated with the control of the hydrophobic matrices essential to their function. [Pg.55]

Functions.—Heparin fractionated by gel filtration appeared to bind to two sites on antithrombin III (association constants 0.6 x 10 and 0.2 x 10 moll" ), whereas heparin prepared by affinity chromatography on matrix-bound antithrombin III appeared to bind to only one site (association constant 2.3 x 10 moll ). These results suggest that one of the binding sites on antithrombin III does not bind the most active heparin components, but accommodates heparin-like molecules which, although similar in size to the active heparin components, have little or no anticoagulant activity. Heparins with high or low affinities for antithrombin III exhibited no differences in their abilities to bind lipoprotein lipase. Studies of the interaction between the lipoprotein lipase from cow s milk and Sepharose-immobilized heparin have shown that heparin is poly-disperse. Whereas heparin facilitated complex formation between a-thrombin and antithrombin III, it had little effect on the interaction between p-thrombin and antithrombin III. ... [Pg.331]

For most analytical processes, a measured signal of the sample is compared with the signals of calibrators in order to calculate the concentration present in the sample. An ideal calibrator contains a known concentration of the analyte and is by all means comparable to the sample to be analysed. As serum contains various protein bound cobalamins and cobalamin analogues in a very complex matrix, it is not possible to use an ideal calibrator when analysing cobalamin in serum. A suitable approximation is a solution of cyanocobalamin prepared as described in Box 26.1. For the final dilution of the calibrator, a buffer comparable to the one used for dilution of the samples to be analysed should be employed. [Pg.456]

Site Isolation Experienced by Matrix-Bound Transition-Metal Complexes... [Pg.424]

Finding the minimum of the hybrid energy function is very complex. Similar to the protein folding problem, the number of degrees of freedom is far too large to allow a complete systematic search in all variables. Systematic search methods need to reduce the problem to a few degrees of freedom (see, e.g.. Ref. 30). Conformations of the molecule that satisfy the experimental bounds are therefore usually calculated with metric matrix distance geometry methods followed by optimization or by optimization methods alone. [Pg.257]

The variational energy principles of classical elasticity theory are used in Section 3.3.2 to determine upper and lower bounds on lamina moduli. However, that approach generally leads to bounds that might not be sufficiently close for practical use. In Section 3.3.3, all the principles of elasticity theory are invoked to determine the lamina moduli. Because of the resulting complexity of the problem, many advanced analytical techniques and numerical solution procedures are necessary to obtain solutions. However, the assumptions made in such analyses regarding the interaction between the fibers and the matrix are not entirely realistic. An interesting approach to more realistic fiber-matrix interaction, the contiguity approach, is examined in Section 3.3.4. The widely used Halpin-Tsai equations are displayed and discussed in Section 3.3.5. [Pg.137]

Complex 1 850 kDa (probably a dimer in membrane) About 40 1 FMN covalently bound, bound 16-24 Fe-S atoms in 5 to 7 centers Spans membrane, NADH site on matrix face, UQ site in membrane 0.06 UQ Pumps protons out of matrix during electron transporl/2e"... [Pg.119]


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See also in sourсe #XX -- [ Pg.424 , Pg.425 , Pg.426 ]




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