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Proportion of bound and

After absorption, a chemical compound enters the circulation, which transfers it to all parts of the body. After this phase, the most important factor affecting the distribution is the passage of the compound through biological membranes. From the point of view of the distribution of a chemical compound, the organism can be divided into three different compartments (1) the plasma compartment (2) the intercellular compartment and (3) the intracellular compartment. In all these compartments, a chemical compound can be bound to biological macromolecules. The proportion of bound and unbound (free) chemical compound depends on the characteristics of both the chemical... [Pg.265]

It has been reported that PSA exists in multiple isoforms in serum free PSA (30-kDa protease) and complexed PS A (100-kDa complex between PSA and A1 ACT). While the PSA in the prostate is in the free form, when the PSA enters the blood stream, the majority binds to A1 ACT. Recent studies have shown that PSA in serum occurs in two molecular forms, free (f-PSA) and bound both PSAs gave equal detectable signals ( equimolar ). Most of the PSA in serum is complexed with either A1 ACT or A2 MG. Different proportions of free and complex isoforms have been detected in the sera of prostate cancer and BPH patients. The fraction... [Pg.188]

Capture ELISA on selected oligomeric fractions of formalin-treated RNase A (see curves 3-7 in Fig. 15.9) also reveal that the plateau values increase with an increase in the number of cross-linked molecules in the fractions. This is due to an increasing proportion of bound epitopes per binding site or, in other words, epitope density on the surface. Thus, the nearly identical plateau values for the titration of native RNase A and formalin-treated unfractionated RNase A (curves 1 and 2 in Fig. 15.9) are fortuitous, being caused by the particular composition of oligomers present in the formalin-treated RNase A preparations that was analyzed. [Pg.267]

The proportion of various Cd forms in soils are shown in Figure 1. water-extractable forms make up 2.0%, adsorbed and exchangeable forms, 57%, carbonate bounded forms, 10.9%, humic bounded forms, 4.8%, occluded forms onto Fe-Mn oxides, 8.1%, organically bounded forms, 8.1%, and residual forms, 9.0%. Proportions of adsorbed and exchangeable forms >carbonate bounded forms>residual forms> occluded forms onto Fe-Mn oxides =organically bounded forms> Humic acid bounded forms... [Pg.95]

There is no agreement on the exact magnitude of the ultrafiltrable or high-molecular-mass fraction of Ni(II) in human serum. Moreover, pronounced species variations in the proportions of ultrafiltrable and protein-bound serum nickel have been demonstrated [289],... [Pg.209]

The first reaction is p-elimination in cysteine, serine, phosphoserine, and threonine residues due to attack by hydroxide ion, leading to the formation of very reactive dehydroalanine (DHA). In a cystine residue, this results in rupturing of the disulfide bond and liberation of a sulfide ion and free sulfur (Figure 13.4). Nucleophilic additions of the s-amino group of the protein-bound lysine to the double bond of DHA residue causes crosslinking of the polypeptide chain. After hydrolysis, a mixture of L-lysino-L-alanine and L-lysino-D-alanine, with probably a small proportion of dl and dd isomers,... [Pg.291]

The problems to be solved are listed hereafter the first problem is the lack of data concerning the exact proportions of low-molecular weight iron complex, ferritin-bound iron and hemosiderin-bound iron (54). However, transverse NMRD profiles of iron-loaded tissues indicate that the transverse relaxation is essentially caused by ferritin, because of the linearity between I/T2 and Bq, which is a fingerprint of ferritin-induced relaxation. The relaxation properties of hemosiderin are less understood. If the proportion of ferritin and hemosiderin is not the same in all of the studied tissues, the correlation between the relaxation properties and the total iron concentration could be affected. [Pg.272]

To establish that a-D-mannosidase is a metalloenzyme, the proportion of bound zinc in the active molecule must first be determined. This experiment has been performed for the enzyme from jack-bean meal.27 Two types of preparation were employed. The first was purified, throughout, at pH 8 without any addition of Zn2+ (see Section 11,4 p. 409). The second enzyme preparation was purified in the presence of added Zn2+ at pH 5 up to stage 5 of the original procedure (see Table V p. 410). It was then freed from unbound Zn2+ by dialysis against glycine buffer of pH 8, and passed through a column of Sephadex G-100 in the same buffer. As may be seen from Table IX, the final specific activity was, in each instance, slightly less than that shown in Table V. [Pg.433]

Keller and coworkers341 proposed that tunicamyein is a reversible, tight-binding, and, therefore, competitive inhibitor of the GlcNAc 1-P transferase. The association rate-constant was 7 x 104 M s 1 (at 23°). Inhibition can be overcome by increasing the proportion of enzyme, and, because preincubation of the enzyme with UDP-GlcNAc prevented inhibition by tunicamyein,341 some experimental support for competitive inhibition was obtained. The known affinity of the antibiotic for phosphonolipids323 may facilitate its access to the membrane-bound enzyme, but the lipids do not prevent inhibition of the enzyme by tunicamyein.340... [Pg.342]

The interaction between proteins and a drug is governed by the law of mass action, in that the proportion of bound drug remains constant, provided the binding sites are not saturated. With the possible exception of valproic acid and disopyramide, the saturability of binding sites does not occur within therapeutic ranges. [Pg.10]

Four major enzyme groups are secreted lipolytic, proteolytic, amylolytic, and nucleic acid splitting enzymes. These pancreatic enzymes, some of which are secreted in multipile forms, possess specificities complementary to die intestinal membrane-bound enzymes (Tabic 1). Fresh, uncontsnkinated pancreatic juice is without proteolytic activity because these enzymes am in the form of inactive zymogens. An important fraction of the calcium in pancreatic juice accompanies the enzymes, especially ct-amylase. Human pancreatic juice is moat dose to that of the pig, with high proportions of lipase and a-amylase in comparison with other mammals [1]. Therefore, pig pancreas extract, pancreatin, has up to now been die oreferred enzvme source for therapeutic tuncreas substitution. [Pg.187]

Other reactions involving this aldehyde include the following (1) combination with sulphite ion, which substantially increases the proportion of bound sulphite in wine (2) formation of addition compounds with some polyphenols such as tannins and procyanidins, where it acts as a bridging molecule (Haslam and Lilley 1998) and (3) chemical oxidation to acetic acid, which only occurs to a small extent and has little influence on wine composition and quality. [Pg.91]

Bisphosphonates are transported through the bloodstream bound to plasma proteins however, the proportion of bound bisphosphonate varies according to agent. For example, the proportions of clodronate, alendronate, and risedronate that bind to human plasma proteins are approximately 40%, 78%, and 24%, respectively [35, 36]. Notable differences exist in... [Pg.549]


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