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In the most trivial application, UV visible spectroscopy provides a means to assess the concentration in solution of proteins or nucleic acids Moreover, calibrated values of A260 and A280 even provide a means to calculate approximate molecular weights according to Equations (44) and (45) However, more substantial structural information remains frustratingly dif cult to deduce Nevertheless, UV visible spectroscopy can be a useful monitor of conformational changes in globular proteins This is possible owing to the effects that local environment may have on the absorbance characteristics of aromatic amino-acid residue chromophores, particularly tryptophan Aromatic amino-acid residues are responsible for clusters of * transitions absorbing strongly in the region 250 300 nm The largest contributors to this UV visible absorbance are tryptophan residues, with more modest contributions coming from tyrosine and phenylalanine residues (Table 41).

Changes in the local environments of these aromatic residues can often be suf cient to change the UV visible absorbance behaviour of some or all of these residues This is particularly true in the event that a globular protein is subject to a range of different physical conditions and/or molecular interactions, which can lead to obvious if not substantial trans-conformational changes, which can provoke changes in local environments and thereby bring about UV visible absorbance changes For instance, many aromatic amino-acid residues are often buried in the hydrophobic interior of a globular protein and not at the hydrophilic surface However, situations arise where conditions change and/or molecular interactions take place that may lead to buried aromatic amino-acid residues entering more hydrophilic environments and becoming more solvent accessible as a consequence of conformational changes (and vice versa).

In such events, energies of both n * and * transitions could become altered in response to changes in the local environments of aromatic amino-acid residues Speci cally, if the local environment of an aromatic amino-acid residue changes from a hydrophobic to a more hydrophilic environment, then a corresponding change in ( ) can lead to a reduction in * transition energies associated with an increase in transition wavelength (red-shift), and an increase in n * transition energies, leading to a decrease in transition wavelength (blue-shift) (Figure 43) (Obviously, the reverse situation is also true if the local environmental changes are from.

(Window Panels Frame, or Ctrl+F/Command+F), to label these, respectively, next, start, and previous. Save the .FLA file.

Frame relay connections are logical connections, not the physical connections of a private line network. Logical connections are sometimes called virtual circuits and the terms are more or less interchangeable. This book prefers the terminology of logical connections because the term virtual has become overworked in the networking industry. There are virtual LANs, virtual private networks, and even several forms of virtual reality. However, the later use of the terms Permanent Virtual Circuit (PVC) and Switched Virtual Circuit (SVC) will be unavoidable. Whatever they are called, the connectivity provided by frame relay networks is logical, not physical. These logical connections form the virtual circuits which replace the dedicated or physical circuits that form the basis of the private line network. This logical connectivity is shown in Figure 1.8.

Before you can make intelligent use of bitmaps in Flash, it s imperative to know about the options for creating bitmaps for use within Flash. That s because all bitmaps are not created equal. A bitmap from one program, created with similar settings, can be twice the file size with no appreciable increase in quality of a bitmap created in another program. It makes no sense to study optimization constraints within Flash if you ignore your exposure to fatty imports. To create a set of controlled images that could be used for comparison, we chose a portrait (with a background that shifts contrast) and a landscape (with a broad expanse of graduated color). Both images were derived from high-quality film shots, scanned at a very high resolution, down-sampled to equivalent dimensions and resolution, 227 287 pixels at 96 ppi, and saved as uncompressed .TIFs. These files were used as the source files from which all other variations were derived (with the sole exception of the double-JPEG example, in which an image that had been previously .JPEG d was used as the source image for the double-JPEG example).