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Native phase

FIGURE 8.6 For any native phase angle p the vector triangle T ru = F/> + fn fails to close by an amount e(p). which is termed the lack of closure error. The phase angle of maximum probability, that for which e(p). is minimized when considered over all isomorphous heavy atom derivatives. [Pg.182]

Fig. 3.19 An example of a temperature-composition diagram showing denaturation of a protein in a native phase into molten globule and fully unfolded phases. The concentrations marked x andy win be used in Exercise 3.39. Fig. 3.19 An example of a temperature-composition diagram showing denaturation of a protein in a native phase into molten globule and fully unfolded phases. The concentrations marked x andy win be used in Exercise 3.39.
The bricks were sectioned, and polished sections were produced for reflected light examination on an optical microscope. In the area of the immediate hot face, i.e., at the slag-brick interface, there was ample evidence of corrosion reactions (Figure 10). Recognizing that the native phases in the brick are... [Pg.56]

We can use the principles of phase equilibrium to leam about the stability of proteins in biological systems. In this example, we consider the phase equilibrium of the protein lysozyme (1) between its native phase, n, and its denatured phase, d, where unfolding occurs. [Pg.324]

SOLUTION A schematic of these two phases at equilibrium is shown in Figure E6.2A. In its native phase, the polymer folds back over itself with the molecules fonning secondary bonds, as shown in the inset in the lower left of the figure. When it becomes denatured, it unfolds as shown in the upper right. As discussed in Example 6.1, the additional bonding in the native state gives it a lower enthalpy relative to the denatured state however, the native state is also more constrained in movement giving it a lower entropy. [Pg.324]

Figure E6.2A Schematic of the equilibrium between the native phase, n, and the denatured phase, d, of the protein lysozyme. The insets show molecular representations of the protein, which unfolds in the denatured phase. Figure E6.2A Schematic of the equilibrium between the native phase, n, and the denatured phase, d, of the protein lysozyme. The insets show molecular representations of the protein, which unfolds in the denatured phase.
For some materials, the most notable being silicon, heating alone sufiBces to clean the surface. Commercial Si wafers are produced with a thin layer of silicon dioxide covering the surface. This native oxide is inert to reaction with the atmosphere, and therefore keeps the underlying Si material clean. The native oxide layer is desorbed, i.e. removed into the gas phase, by heating the wafer in UHV to a temperature above approximately 1100 °C. This procedure directly fonus a clean, well ordered Si surface. [Pg.303]

Referring to figure Bl.8.5 the radii of the tliree circles are the magnitudes of the observed structure amplitudes of a reflection from the native protein, and of the same reflection from two heavy-atom derivatives, dl and d2- We assume that we have been able to detemiine the heavy-atom positions in the derivatives and hl and h2 are the calculated heavy-atom contributions to the structure amplitudes of the derivatives. The centres of the derivative circles are at points - hl and - h2 in the complex plane, and the three circles intersect at one point, which is therefore the complex value of The phases for as many reflections as possible can then be... [Pg.1376]

Limitations with the chiral selectivity of the native cyclodextrins fostered the development of various functionalized cyclodextrin-based chiral stationary phases, including acetylated (82,83), sulfated (84), 2-hydroxypropyl (85), 3,5-dimethylphenylcarbamoylated (86) and... [Pg.65]

As mentioned previously, cellulosic phases as well as amylosic phases have also been used extensively for enantiomeric separations more recently (89,90). Most of the work ia this area has been with various derivatives of the native carbohydrate. The enantioresolving abiUties of the derivatized cellulosic and amylosic phases are reported to be very dependent on the types of substituents on the aromatic moieties that are appended onto the native carbohydrate (91). Table 3 fists some of the cellulosic and amylosic derivatives that have been used. These columns are available through Chiral Technologies, Inc. and J. T. Baker, Inc. [Pg.66]

Gyclodextrins. As indicated previously, the native cyclodextrins, which are thermally stable, have been used extensively in Hquid chromatographic chiral separations, but their utihty in gc appHcations was hampered because their highly crystallinity and insolubiUty in most organic solvents made them difficult to formulate into a gc stationary phase. However, some functionali2ed cyclodextrins form viscous oils suitable for gc stationary-phase coatings and have been used either neat or diluted in a polysiloxane polymer as chiral stationary phases for gc (119). Some of the derivati2ed cyclodextrins which have been adapted to gc phases are 3-0-acetyl-2,6-di-0-pentyl, 3-0-butyryl-2,6-di-0-pentyl,... [Pg.70]

Cellulose I. The majority of celluloses in the native state were previously thought to have the same crystal stmcture (Cellulose I), varying only in perfection of the crystaUites. Now, at least two different crystal stmctures are known for these materials, named la and ip. These two phases coexist in... [Pg.240]

In the development of new products, optimization of the fermentation medium for titer only often ignores the consequences of the medium properties on subsequent downstream processing steps such as filtration and chromatography. It is imperative, therefore, that there be effective communication and understanding between workers on the upstream and downstream phases of the produc t development if rational trade-offs are to be made to ensure overall optimahty of the process. One example is to make the conscious decision, in collaboration with those responsible for the downstream operations, whether to produce a protein in an unfolded form or in its native folded form the purification of the aggregated unfolded proteins is simpler than that of the native protein, but the refolding process itself to obtain the product in its final form may lack scalabihty. [Pg.2057]

Vapor-phase decomposition and collection (Figs 4.16 to 4.18) is a standardized method of silicon wafer surface analysis [4.11]. The native oxide on wafer surfaces readily reacts with isothermally distilled HF vapor and forms small droplets on the hydrophobic wafer surface at room temperature [4.66]. These small droplets can be collected with a scanning droplet. The scanned, accumulated droplets finally contain all dissolved contamination in the scanning droplet. It must be dried on a concentrated spot (diameter approximately 150 pm) and measured against the blank droplet residue of the scanning solution [4.67-4.69]. VPD-TXRF has been carefully evaluated against standardized surface analytical methods. The user is advised to use reliable reference materials [4.70-4.72]. [Pg.192]

Native biological membranes also display characteristic phase transitions, but these are broad and strongly dependent on the lipid and protein composition of the membrane. [Pg.269]

Nowadays, almost all commercially available HPLC stationary phases are also applicable to planar chromatography. In addition to the polar hydroxyl groups present on the surface of native silica, other polar functional groups attached to the silica skeleton can also enter into adsorptive interactions with suitable sample molecules (34). Silica with hydrophilic polar ligands, such as amino, cyano, and diol functions, attached to the silica skeleton by alkyl chains, all of which have been well proven in HPLC, have also been developed for TLC (34). [Pg.186]

Mourier s report was quickly followed by successful enantiomeric resolutions on stationary phases bearing other types of chiral selectors, including native and deriva-tized cyclodextrins and derivatized polysaccharides. Many chiral compounds of pharmaceutical interest have now been resolved by packed column SFC, including antimalarials, (3-blockers, and antivirals. A summary is provided in Table 12-2. Most of the applications have utilized modified CO, as the eluent. [Pg.303]

The major differences between polymer and liquid electrolytes result from the physical stiffness of the PE. PEs are either hard-to-soft solids, or a combination of solid and molten in phases equilibrium. As a result, wetting and contact problems are to be expected at the Li/PE interface. In addition, the replacement of the native oxide layer covering the lithium, under the... [Pg.446]

Unfortunately, silica gel suffers from a severe disadvantage in that it is slightly soluble in water. This means that the native silica cannot be used in conjunction with aqueous mobile phases. Consequently, silica is precluded from use in the separation of those substances that are strongly polar and require aqueous solvents to render them soluble and stable. For this reason the relatively new, micro-reticular resins are now used in the separation of strongly polar substances by exclusion chromatography. [Pg.286]


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See also in sourсe #XX -- [ Pg.109 ]




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Native solid-phase synthesis

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