The human T1R2-T1R3 sweet taste receptor (STR) plays an important role in recognizing various low-molecular-weight sweet-tasting sugars and proteins, resulting in the release of intracellular heterotrimeric G protein ...
The human T1R2-T1R3 sweet taste receptor (STR) plays an important role in recognizing various low-molecular-weight sweet-tasting sugars and proteins, resulting in the release of intracellular heterotrimeric G protein that in turn leads to the sweet taste perception. Xylitol and sorbitol, which are naturally occurring sugar alcohols (polyols) found in many fruits and vegetables, exhibit the potential caries-reducing effect and are widely used for diabetic patients as low-calorie sweeteners. In the present study, computational tools were applied to investigate the structural details of binary complexes formed between these two polyols and the T1R2-T1R3 heterodimeric STR. Principal component analysis revealed that the Venus flytrap domain (VFD) of T1R2 monomer was adapted by the induced-fit mechanism to accommodate the focused polyols, in which α-helical residues 233-268 moved significantly closer to stabilize ligands. This finding likely suggested that these structural transformations might be the important mechanisms underlying polyols-STR recognitions. The calculated free energies also supported the VFD of T1R2 monomer as the preferential binding site for such polyols, rather than T1R3 region, in accord with the lower number of accessible water molecules in the T1R2 pocket. The E302 amino acid residue in T1R2 was found to be the important recognition residue for polyols binding through a strongly formed hydrogen bond. Additionally, the binding affinity of xylitol toward the T1R2 monomer was significantly higher than that of sorbitol, making it a sweeter tasting molecule.
Currently, textile materials with multifunctional properties have considerably attracted more and more attention in scientific community. In this work, multi-properties of polypropylene (PP) spunbond nonwoven fabric i...
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Adhesion property of natural rubber (NR) and reclaimed natural rubber (RNR) based sealant with concrete was studied here. The effect of tackifier type and loading on the tensile properties of the rubber based sealant ...
Adhesion property of natural rubber (NR) and reclaimed natural rubber (RNR) based sealant with concrete was studied here. The effect of tackifier type and loading on the tensile properties of the rubber based sealant sandwished between two flat cements was evaluated. There are three different tackifiers including Coumarone-indene resin (CI), petro resin (PE) and gum rosin (GR). The result initially showed that at the 20 phr of tackifier both NR and RNR sealant mixed with CI consumed the highest force to separate the rubber based sealant from the concrete. This might be due to the highest compatiblility between CI and rubber. Regardless of the tackifier type, all NR based sealants showed the cohesive failure while all RNR based sealants only showed the adhesive failure. Moreover, the NR based sealant seemed to be stronger than the RNR based one. When considering the effect of CI loading on the adhesion, it was shown that for both NR and RNR based sealents, the highest stress was observed when the rubber based sealant loaded with the 20 phr of CI.
A series of imbiber terpolymer beads was prepared by radical suspension copolymerization of styrene–divinylbenzene with varied contents of acrylated vinyl monomers, n‐ butyl acrylate and 2‐ethyl hexyl acrylate, as ...
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Crosslinked poly(meth)acrylate polymers with a variety of morphologies were synthesized with two steps. In the first step, a microporous glass membrane (Shirasu Porous Glass, SPG) was employed to prepare uniform emuls...
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Crosslinked poly(meth)acrylate polymers with a variety of morphologies were synthesized with two steps. In the first step, a microporous glass membrane (Shirasu Porous Glass, SPG) was employed to prepare uniform emulsion droplets by applying an adequate pressure to the monomer phase, which was composed of the ADVN initiator, solvent of toluene or heptane or their mixture, and a mixture of (meth)acrylate monomers. The droplets were formed continuously through the membrane and suspended in the aqueous solution, which contained a PVA-127 suspending agent, SLS emulsifier, and NaNO 2 inhibitor to suppress the nucleation of secondary particles. SPG pore sizes of 0.90, 5.25, and 9.25 μm were used. Then the emulsion droplets were polymerized at 343 K with a rotation rate 160 rpm for 24 h. The (meth)acrylate monomers 2-ethylhexyl acrylate (2-EHA), 2-ethylhexyl methacrylate (2-EHMA), cyclohexyl acrylate (CHA), methyl methacrylate (MMA), lauryl acrylate (LA), and lauryl methacrylate (LMA) were used in this research. The influences of the ratios of the monomer and crosslinking agent EGDMA, the amount of diluents, the monomer type on the polymer particle morphology, the swelling degree, and the polymer particle size were investigated. It was found that an increase in the concentrations of EGDMA and heptane resulted in higher coarse porous spheres and smaller polymer particle sizes. A coefficient with a variation close to 10%, or a standard deviation of about 4, was obtained. The capacity of these spheres as solvent absorption materials was examined. The highest swelling degrees of heptane and toluene were obtained when LA was employed as the monomer with 30% (by weight) of EGDMA and 70% (by weight) of heptane as an inert solvent. The highest capacity of the solvent absorption was obtained when using a polymer particle size of 4.81 μm, as prepared by SPG pore size 0.9 μm. The polymer particles were able to absorb aliphatic hydrocarbon solvents, aromatic hydrocarbon solvents, and
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