Hydration conformation changes with

More advanced semiempirical molecular orbital methods have also been used in this respect in modeling, e.g., the structure of a diphosphonium extractant in the gas phase, and then the percentage extraction of zinc ion-pair complexes was correlated with the calculated energy of association of the ion pairs [29]. Semiempirical SCF calculations, used to study structure, conformational changes and hydration of hydroxyoximes as extractants of copper, appeared helpful in interpreting their interfacial activity and the rate of extraction [30]. Similar (PM3, ZINDO) methods were also used to model the structure of some commercial extractants (pyridine dicarboxylates, pyridyloctanoates, jS-diketones, hydroxyoximes), as well as the effects of their hydration and association with modifiers (alcohols, )S-diketones) on their thermodynamic and interfacial activity [31 33]. In addition, the structure of copper complexes with these extractants was calculated [32]. 

Water binding varies with the number and type of polar groups (5 ). Other factors that affect the mechanism of protein-water interactions include protein conformation and environmental factors that affect protein polarity and/or conformation. Conformational changes in the protein molecules can affect the nature and availability of the hydration sites. Transition from globular to random coil conformation may expose previously buried amino acid side chains, thereby making them available to interact with aqueous medium. Consequently, an unfolded conformation may permit the protein to bind more water than was possible in the globular form ( ). 

Wilkes et al (22.23) coupled calorimetric, dynamic-mechanical and x-ray diffraction techniques to demonstrate crystallization of the lipids was completely reversible in neonatal rat stratum corneum, and only partially reversible in human stratum corneum. Melting regions near 40°C and from 70 to 90°C corresponded to the thermal transitions noted in the calorimetric studies for both species. The crystalline nature of the lipids did not appear to be dependent on the presence of water. X-ray diffraction and infrared spectroscopy studies (23.28-34) have also shown a to p conformational changes occurred in keratin and stratum corneum protein components with hydration or exposure to increased temperatures. Oertel (28) has reported pretreatment with dimethylsulfox-ide, hexylmethylsulfoxide and decylmethylsulfoxide resulted in the formation of p-sheet protein conformations in vitro in human... 

There is evidence that the a-cyclodextrin macrocycle can adjust its cavity diameter, within certain limits, to accommodate either two hydrate water molecules in the collapsed or tense form, or a nonaqueous guest molecule in the round or relaxed form. This is the concept of the induced fit [576] which has been applied to comparable conformational changes observed with several enzymes upon substrate binding. 

DNA is fully hydrated with about 20 water molecules per nucleotide [522, 853-862], as indicated in Fig. 24.2. The hydration depends strongly on the water activity aw, which can be adjusted by addition of salt. At and above complete hydration, B-DNA prevails. It changes to some other conformation if the hydration is reduced, to an attainable minimum of 3.6 water molecules per nucleotide. If water is added in excess, the sample swells but remains in the B-DNA form [856, 857]. 

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