|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Use ofbiomolecular templates for the fabrication of metal nanowires显示文摘 | Ehud Gazit | 2007 | FEBS Journal2007，274，： | 1 |
| 2 | Spacer driven morphological twist in Phe-Phe dipeptide conjugates 显示文摘 | Surajit Ghosh Lihi Adler-Abramovich Ehud Gazit | 2013 | Tetrahedron2013，69，8： | 1 |
| 3 | Casting metal nanowires within discrete self-assembled peptide nanotubes显示文摘 | Meital Reches Ehud Gazit | 2003 | Science2003，300，5619： | 1 |
| 4 | Global analysis of tandenm aromatic octapeptide repeats:The significance ofthe aromatic-glycine motif显示文摘 | Ehud Gazit | 2002 | Discovery Note2002，18，6： | 1 |
| 5 | Improved design of the Vivaldi antenna 显示文摘 | Ehud Gazit | 1988 | IEE Proceedings1988，135，2： | 1 |
| 6 | Piezoelectric Peptide and Metabolite Materials显示文摘Piezoelectric materials are important for many physical and electronic devices.Although many piezoelectric ceramics exhibit good piezoelectricity,they often show poor compatibility with biological systems that limits their biomedical applications.Piezoelectric peptide and metabolite materials benefit from their intrinsic biocompatibility,degradability,and convenient biofunctionalization and are promising candidates for biological and medical applications.Herein,we provide an account of the recent progress of research works on piezoelectric peptide and metabolite materials.This review focuses on the growth mechanism of peptide and metabolite micro-and nanomaterials.The influence of self-assembly processes on their piezoelectricity is discussed.Peptide and metabolite materials demonstrate not only outstanding piezoelectric properties but also unique electronic,optical,and physical properties,enabling their applications in nanogenerators,sensors,and optical waveguiding devices. | Hui Yuan Peipei Han Kai Tao Shuhai Liu Ehud Gazit Rusen Yang | 2019 | Research2019，，1： | 0 |
| 7 | 作为基础的生物学的广阔发展空间显示文摘作为21世纪最重要的两门学科,纳米科技与生物科技受到了全世界科学家的关注与研究。本书为广大读者呈现的是将纳米科技与生物科技融为一体的新学科——生物纳米科技/纳米生物科技。 | Ehud Gazit 程恩隽 | 2008 | 国外科技新书评介2008，，9： | 0 |
| 8 | Modulating vectored non-covalent interactions for layered assembly with engineerable properties显示文摘Vectored non-covalent interactions—mainly hydrogen bonding and aromatic interactions—extensively contribute to(bio)-organic self-assembling processes and significantly impact the physicochemical properties of the associated superstructures.However,vectored non-covalent interaction-driven assembly occursmainly along one-dimensional(1D)or three-dimensional(3D)directions,and a two-dimensional(2D)orientation,especially that of multilayered,graphene-like assembly,has been reported less.In this present research,by introducing amino,hydroxyl,and phenyl moieties to the triazine skeleton,supramolecular layered assembly is achieved by vectored non-covalent interactions.The planar hydrogen bonding network results in high stability,with a thermal sustainability of up to about 330°C and a Young’s modulus of up to about 40 GPa.Upon introducing wrinkles by biased hydrogen bonding or aromatic interactions to disturb the planar organization,the stability attenuates.However,the intertwined aromatic interactions prompt a red edge excitation shift effect inside the assemblies,inducing broad-spectrum fluorescence covering nearly the entire visible light region(400–650 nm).We show that bionic,superhydrophobic,pillar-like arrays with contact angles of up to about 170°can be engineered by aromatic interactions using a physical vapor deposition approach,which cannot be realized through hydrogen bonding.Our findings show the feasibility of 2D assembly with engineerable properties by modulating vectored non-covalent interactions. | Jiahao Zhang Sarah Guerin Haoran Wu Bin Xue Yi Cao Syed A.M.Tofail Yancheng Wang Damien Thompson Wei Wang Kai Tao Deqing Mei Ehud Gazit | 2022 | Bio-Design and Manufacturing2022，5，3： | 0 |
| 9 | Rational Design of Biological Crystals with Enhanced Physical Properties by Hydrogen Bonding Interactions显示文摘Hydrogen bonds are non-covalent interactions and essential for assembling supermolecules into ordered structures in biological systems,endowing crystals with fascinating physical properties,and inspiring the construction of eco-friendly electromechanical devices.However,the interplay between hydrogen bonding and the physical properties is not fully understood at the molecular level.Herein,we demonstrate that the physical property of biological crystals with double-layer structures could be enhanced by rationally controlling hydrogen bonding interactions between amino and carboxyl groups.Different hydrogen bonding interactions result in various thermal,mechanical,electronic,and piezoelectric properties.In particular,the weak interaction between O and H atoms contributes to low mechanical strength that permits important ion displacement under stress,giving rise to a strong piezoelectric response.This study not only reveals the correlation between the hydrogen bonding and physical properties in double-layer structures of biological crystals but also demonstrates the potential of these crystals as functional biomaterials for high-performance energy-harvesting devices.Theoretical calculations and experimental verifications in this work provide new insights into the rational design of biomaterials with desirable physical properties for bioelectrical devices by modulating intermolecular interactions. | Hui Yuan Bin Xue Dingyi Yang Sigal Rencus-Lazar Yi Cao Ehud Gazit Dan Tan Rusen Yang | 2023 | Research2023，，3： | 0 |
| 10 | Bio-organic adaptive photonic crystals enable supramolecular solvatochromism显示文摘Photonic crystals(PCs)exhibit promising structural coloration properties and possess extensive application prospects in diverse optical fields.However,state-of-the-art inorganic or polymeric PCs show limited adaptivity as their configurations are fixed once formed.Herein,bio-organic adaptive PCs are fabricated via drop-casting of amphiphilic guanine-based peptide nucleic acid selfassembled microspheres.The high formation activation energy of up to 81.8 kJ·mol−1 suggests that the self-assembly step dominates the entire process.Therefore,the configurations along with the structural coloration of the supramolecular PCs are sensitive to self-assembly influencing parameters,showing temperature-encoded structural color evolution and solvent polaritydependent solvatochromism.Our findings demonstrate that the supramolecular PCs are adaptive,thus showing promising potential for detection of organic solvents of different polarities in a visual and real-time manner for environmental protection or optical applications. | Jiahao Zhang Yan Zhang Yancheng Wang Sigal Rencus-Lazar Deqing Mei Ehud Gazit Kai Tao | 2023 | Nano Research2023，16，10： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员