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141.
An amphiphilic poly(L ‐lysine·HBr)‐block‐poly(L ‐leucine) (KL) diblock copolypeptide and its supramolecular assembly are used as a template to direct silica formation, which proceeds by a cooperative process involving biomimetic mineralization and copolypetide reassembly under ambient conditions. Various silica structures can be obtained by using different counterions, changing the chain length of the KL diblocks, and applying a sol–gel mineralization method. We find that the chain length of the KL diblock is an important factor in terms of controlling biosilica morphologies. We also find that the nature of the counterions strongly affects the resulting silica structures. For the same KL diblock, variation of anions from phosphate to sulfate and to carbonate can produce hexagonal silica platelets, silica rods, and fused silica platelets, respectively. In contrast, application of a sol–gel method can replicate the copolypeptide fibril network morphology in water, while employment of ultrasonication to the sol–gel medium transforms the silica fibrils to rigid silica rods. The resulting silica morphology has been systematically characterized using SEM and TEM, and the polypeptide conformation is explored using FT‐IR and CD spectroscopy.
142.
Wei‐Shi Li Prof. Dr. Akinori Saeki Dr. Yohei Yamamoto Dr. Takanori Fukushima Dr. Shu Seki Prof. Dr. Noriyuki Ishii Dr. Kenichi Kato Dr. Masaki Takata Prof. Dr. Takuzo Aida Prof. Dr. 《化学:亚洲杂志》2010,5(7):1566-1572
To tailor organic p/n heterojunctions with molecular‐level precision, a rational design strategy using side‐chain incompatibility of a covalently connected donor–acceptor (D–A) dyad has been successfully carried out. An oligothiophene–perylenediimide dyad, when modified with triethylene glycol side chains at one terminus and dodecyl side chains at the other ( 2 Amphi ), self‐assembles into nanofibers with a long‐range D/A heterojunction. In contrast, when the dyad is modified with dodecyl side chains at both termini ( 2 Lipo ), ill‐defined microfibers result. In steady‐state measurements using microgap electrodes, a cast film of the nanofiber of 2 Amphi displays far better photoconducting properties than that of the microfiber of 2 Lipo . Flash‐photolysis time‐resolved microwave conductivity measurements, in conjunction with transient absorption spectroscopy, clearly indicate that the nanofiber of 2 Amphi intrinsically allows for better carrier generation and transport properties than the microfibrous assembly of 2 Lipo . 相似文献
143.
Emilie Barriau Alejandra García Marcos Holger Kautz Holger Frey 《Macromolecular rapid communications》2005,26(11):862-867
Summary: A convenient three‐step strategy has been developed for the preparation of well‐defined amphiphilic, linear‐hyperbranched block copolymers by hypergrafting. The synthetic procedure is based on a combination of carbanionic polymerization with the alkoxide‐based, controlled ring‐opening multibranching polymerization of glycidol. A linear AB diblock copolymer polystyrene‐block‐polybutadiene (PS‐b‐PB) with narrow polydispersity was obtained by anionic copolymerization. Subsequent hydroxylation by hydroboration led to PS508‐b‐(PB‐OH)56, used as macroinitiator for the polymerization of glycidol under slow monomer addition conditions.
144.
Dr. Lubna Ghani Dr. Seonghoon Kim Dr. Haoqing Wang Hyun Sung Lee Dr. Jonas S. Mortensen Dr. Satoshi Katsube Dr. Yang Du Dr. Aiman Sadaf Dr. Waqar Ahmed Prof. Bernadette Byrne Prof. Lan Guan Prof. Claus J. Loland Prof. Brian K. Kobilka Prof. Wonpil Im Prof. Pil Seok Chae 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(21):e202200116
Membrane proteins are of biological and pharmaceutical significance. However, their structural study is extremely challenging mainly due to the fact that only a small number of chemical tools are suitable for stabilizing membrane proteins in solution. Detergents are widely used in membrane protein study, but conventional detergents are generally poor at stabilizing challenging membrane proteins such as G protein-coupled receptors and protein complexes. In the current study, we prepared tandem triazine-based maltosides (TZMs) with two amphiphilic triazine units connected by different diamine linkers, hydrazine (TZM−Hs) and 1,2-ethylenediamine (TZM−Es). These TZMs were consistently superior to a gold standard detergent (DDM) in terms of stabilizing a few membrane proteins. In addition, the TZM−Es containing a long linker showed more general protein stabilization efficacy with multiple membrane proteins than the TZM−Hs containing a short linker. This result indicates that introduction of the flexible1,2-ethylenediamine linker between two rigid triazine rings enables the TZM−Es to fold into favourable conformations in order to promote membrane protein stability. The novel concept of detergent foldability introduced in the current study has potential in rational detergent design and membrane protein applications. 相似文献
145.
Enzo Bomal Dr. Vincent Croué Dr. Reuben Yeo Dr. Rosario Scopelliti Prof. Holger Frauenrath 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(41):8907-8915
Oligoynes with two or more conjugated carbon–carbon triple bonds are useful precursors for carbon-rich nanomaterials. However, their range of applications has so far been severely limited by the challenging syntheses, particularly in the case of oligoynes with functional groups. Here, we report a universal synthetic approach towards both symmetric and unsymmetric, functionalized hexaynes through the use of a modified Eglinton–Galbraith coupling and a sacrificial building block. We demonstrate the versatility of this approach by preparing hexaynes functionalized with phosphonic acid, carboxylic acid, ammonium, or thiol head groups, which serve as neutral, cationogenic, or anionogenic interfacially active groups. We show that these hexaynes are carbon-rich amphiphiles or bolaamphiphiles that self-assemble at liquid–liquid interfaces, on solid surfaces, as well as in aqueous media. 相似文献
146.
Anton Zalygin Daria Solovyeva Ivan Vaskan Dr. Stephen Henry Dr. Marcel Schaefer Dr. Pavel Volynsky Dr. Alexander Tuzikov Dr. Elena Korchagina Dr. Ivan Ryzhov Dr. Alexey Nizovtsev Dr. Konstantin Mochalov Prof. Roman Efremov Dr. Eleonora Shtykova Dr. Vladimir Oleinikov Prof. Nicolai Bovin 《ChemistryOpen》2020,9(6):641-648
The synthetic function-spacer-lipid (FSL) amphiphile biotin-CMG-DOPE is widely used for delicate ligation of living cells with biotin residues under physiological conditions. Since this molecule has an “apolar-polar-hydrophobic” gemini structure, the supramolecular organization is expected to differ significantly from the classical micelle. Its organization is investigated with experimental methods and molecular dynamics simulations (MDS). Although the linear length of a single biotin-CMG-DOPE molecule is 9.5 nm, the size of the dominant supramer globule is only 14.6 nm. Investigations found that while the DOPE tails form a hydrophobic core, the polar CMG spacer folds back upon itself and predominantly places the biotin reside inside the globule or planar layer. MDS demonstrates that <10 % of biotin residues on the highly water dispersible globules and only 1 % of biotin residues in layer coatings are in an linear conformation and exposing biotin into the aqueous medium. This explains why in biotin-CMG-DOPE apolar biotin residues both in water dispersible globules and coatings on solid surfaces are still capable of interacting with streptavidin. 相似文献
147.
We designed multiblock amphiphiles AmF and AmH , which consist of perfluorinated and non-fluorinated hydrophobic units, respectively. Absorption spectroscopy revealed that both amphiphiles are molecularly dispersed in organic solvent, while they form aggregates under aqueous conditions. Furthermore, we investigated whether AmF and AmH can be incorporated into DOPC lipid bilayer membranes, and found that the maximum concentration of AmF that can be incorporated into DOPC lipid bilayer membranes is 43 times higher than that of AmH . 相似文献
148.
Kolattukudy Poulose Santo Andriy Kovalenko Maria Stepanova 《Macromolecular theory and simulations》2010,19(5):228-239
Three‐dimensional mesoscopic morphologies and the thermodynamics of structural phase transitions of amphiphilic lipids at air‐water interfaces are studied using self‐consistent field theory. Changing the relative amount of lipids in the system led to a series of 3D morphologic phases with varying average interfacial area per molecule, mimicking a compression of the model membranes. Membranes of both saturated and unsaturated lipids undergo a transition from cylindrical micelle to lamella when the lipid content in the system increases from 2% to about 19–20%. With further increase in the lipid content, saturated lipids first develop non‐uniform quasi‐2D distributions in the lamella and then gradually transform into a hybrid morphology containing quasi‐planar lamellae. In contrast, unsaturated lipids develop reverse‐micellar morphologies.
149.