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Cellular Fatty Acid-Binding Proteins II - Proceedings of the 2nd International Workshop on Fatty Acid-Binding Proteins, Maastricht, August 31 and September 1, 1992 (Paperback, Softcover reprint of the original 1st ed. 1993)
Loot Price: R5,452
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Cellular Fatty Acid-Binding Proteins II - Proceedings of the 2nd International Workshop on Fatty Acid-Binding Proteins, Maastricht, August 31 and September 1, 1992 (Paperback, Softcover reprint of the original 1st ed. 1993)
Series: Developments in Molecular and Cellular Biochemistry, 10
Expected to ship within 10 - 15 working days
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The cellular functions of lipid-transport proteins cannot can be
obtained, as well as structural information re- garding the local
environment of the spectroscopic be fully realized without a
comprehensive knowledge of probe. However, changes in protein
fluorescence upon their binding properties. In particular, it is
important to identify physiologically important ligands and
establish ligand binding are sometimes too small to quantitate.
their binding affinities, stoichiometries and specificities. This
is particularly true for L-FABP, which has no tryp- Since many
lipid-binding proteins exhibit no enzymatic tophan residues. Also,
some lipids lack intrinsic fluores- cence or paramagnetic
properties, including many lipids activity, binding parameters
provide an important quan- titative measure for comparing the
'activity' of various of physiological interest. In such cases,
lipid analogues wild-type and mutant forms. For this purpose,
binding containing structure-perturbing anthroylxoxy or doxyl
assays that are quantitative, accurate and robust are de- probes
are required. Lipids that do have intrinsic fluor- sirable.
escence, such as parinaric acid, are labile and prone to For the
intracellular fatty acid- and lipid-binding pro- oxidation. The
binding of native ligands can be moni- teins, a variety of
biochemical and biophysical binding tored by isotope-directed NMR
techniques, provided assays have been used. The biochemical assays
include that enrichment with 13C or another suitable isotope is
those based on gel-filtration [1-3], equilibrium dialysis feasible.
Although such NMR methods are useful for de- [4], Lipidex [5,6] and
liposomes [7].
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