Hydrophobically modified, interaction with

Slepnev, V., et al. 1995. Fatty acid acylated peroxidase as a model for the study of interactions of hydrophobically-modified proteins with mammalian cells. Bioconjug Chem 6 608. 

Mizusaki M, Morishima Y, Dubin PL. Interaction of pyrene-labeled hydrophobically modified polyelectrolytes with oppositely charged mixed micelles studied by fluorescence quenching. J Phys Chem 1998 102 1908-1915. 

Bu, H., Kj0niksen, A.L., Elgsaeter, A., Nystrom, B. Interaction of unmodified and hydrophobically modified alginate with sodium dodecylsulfate in dilute aqueous solution. Calorimetric, rheological, and turbidity studies. Colloids Surf. A Physicochem. Eng. Aspects 278, 166-174 (2006)... 

Gasnier et al. [138] also reported the catalytic determination of reduced nicotinamide adenine dinucleotide (NADH) at very low potentials (-0.25V), with excellent sensitivity and stability by using a G CE modified with PEI functionalized with Do and glutaraldehyde as a linker (PEI-Glu-Do). The presence of Do covalently bonded to PEI promotes hydrophobic x-interactions with the CNT walls conferring better stability and mechanical strength to the dispersion compared with nonmodified PEI. 

In reality, many proteins demonstrate mixed mode interactions (e.g., additional hydrophobic or silanol interactions) with a column, or multiple structural conformations that differentially interact with the sorbent. These nonideal interactions may distribute a component over multiple gradient steps, or over a wide elution range with a linear gradient. These behaviors may be mitigated by the addition of mobile phase modifiers (e.g., organic solvent, surfactants, and denaturants), and optimization (temperature, salt, pH, sample load) of separation conditions. 

A class of systems extensively investigated by means of PFG-NMR are colloids. They are usually hydrophobically modified water-soluble polymers, that is, polymers with a water-soluble skeleton bearing one or more hydrophobic units, which allow the self-assembling of the polymer in water solution and the interaction with surfactants.77... 

Many other types of solid phase adsorbents, including those based on conventional and specialty materials like restricted access media (RAM), can increase analysis speed and improve assay performance. These types of materials, also known as internal reversed-phase packings, are especially useful for assaying target compounds in biological samples such as serum and plasma. They are chemically modified porous silicas that have hydrophilic external surfaces and restricted-access hydrophobic internal surfaces. The ratio of interior to external surface areas is large. Macromolecules such as proteins cannot enter the pores of the RAM (they are excluded from the hydrophobic internal surface) and they elute quickly through the column. However, the smaller analyte molecules that can enter the pores are retained via interactions with the hydrophobic bonded phase within... 

Modified silica with a C18 reversed-phase sorbent has historically been the most popular packing material, owing to its greater capacity compared to other bonded silicas, such as the C8 or CN types [22]. Applications of C18 sorbents include the isolation of hydrophobic species from aqueous solutions. The mechanism of interaction with such sorbents depends on van der Waals forces, and secondary interactions such as hydrogen bonding and dipole-dipole interactions. Nevertheless, the main drawbacks of such sorbents are their limited breakthrough volumes for polar analytes, and their narrow pH stability range. For these reasons, reversed-phase polymeric sorbents are also used frequently in environmental applications for the trace enrichment of soluble molecules that are not isolated by reversed-phase sorbents such as C18. 

Thus, lipoproteins could be injected over the surface of a lipid covered SPR sensor in a detergent free buffer solution and showed spontaneous insertion into the artificial membrane.171 Again two hydro-phobic modifications are necessary for stable insertion into the lipid layer, whereas lipoproteins with a farnesyl group only dissociate significantly faster out of the membrane. Therefore the isoprenylation of a protein is sufficient to allow interaction with membraneous structures, while trapping of the molecule at a particular location requires a second hydrophobic anchor. Interaction between the Ras protein and its effector Raf-kinase depends on complex formation of Ras with GTP (instead of the Ras GDP complex, present in the resting cell). If a synthetically modified Ras protein with a palmi-... 

Anions and uncharged analytes tend to spend more time in the buffered solution and as a result their movement relates to this. While these are useful generalizations, various factors contribute to the migration order of the analytes. These include the anionic or cationic nature of the surfactant, the influence of electroendosmosis, the properties of the buffer, the contributions of electrostatic versus hydrophobic interactions and the electrophoretic mobility of the native analyte. In addition, organic modifiers, e.g. methanol, acetonitrile and tetrahydrofuran are used to enhance separations and these increase the affinity of the more hydrophobic analytes for the liquid rather than the micellar phase. The effect of chirality of the analyte on its interaction with the micelles is utilized to separate enantiomers that either are already present in a sample or have been chemically produced. Such pre-capillary derivatization has been used to produce chiral amino acids for capillary electrophoresis. An alternative approach to chiral separations is the incorporation of additives such as cyclodextrins in the buffer solution. 

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