- 标题
- 摘要
- 关键词
- 实验方案
- 产品
-
Dependance of Poly(acrylic acid) Interfacial Adhesion on the Nanostructure of Electrodeposited ZnO Films
摘要： Understanding the impact of the intricate morphology and surface chemistry of ZnO nanorod arrays on their interactions with polyelectrolyte polymers is crucial for the development of nascent ZnO-based adhesion-promoting materials. AFM based Single Molecule Force Spectroscopy (SMFS) was applied for the analysis of the adsorption of poly(acrylic acid) (PAA) on zinc oxide (ZnO) film covered stainless steel substrates in aqueous electrolytes at pH 7. Based on the electrodeposition process, the morphology of zinc oxide films could be varied ranging from platelet-like crystals to nanorods. This approach allowed for the morphology dependent analysis of macromolecular adsorption processes on complex ZnO nanostructures which have diverse applications in the field of adhesion-promoting thin films. The surface chemical composition, as determined by X-ray photoelectron spectroscopy, could be correlated to the AFM-based desorption studies. Only equilibrium desorption events (plateaus), centered at 42 pN, were observed on mirror polished, preconditioned stainless steel. However, for platelet-like ZnO films, the poly(acrylic acid) desorption showed a mixture of rupture events (mean rupture forces of about 350 pN) and equilibrium desorption, while ZnO nanorod structures showed solely rupture events with mean rupture forces of about 1300 pN. These results indicate that simultaneous multiple ruptures of carboxylate-zinc bonds occur due to the macromolecular coordination of poly(acrylic acid) to the ZnO nanorods. The analysis of the interfacial adhesion processes is further supported by the dwell time dependence of desorption processes.
关键词： poly(acrylic acid),Single Molecule Force Spectroscopy (SMFS),worm like chain (WLC) model,stainless steel,zinc oxide (ZnO),electrochemical deposition,molecular adhesion,adsorption free energy
更新于2025-09-19 17:15:36
-
[Methods in Molecular Biology] Atomic Force Microscopy Volume 1886 (Methods and Protocols) || Molecular Recognition Force Spectroscopy for Probing Cell Targeted Nanoparticles In Vitro
摘要： In the development and design of cell targeted nanoparticle-based systems the density of targeting moieties plays a fundamental role in allowing maximal cell-specific interaction. Here, we describe the use of molecular recognition force spectroscopy as a valuable tool for the characterization and optimization of targeted nanoparticles toward attaining cell-specific interaction. By tailoring the density of targeting moieties at the nanoparticle surface, one can correlate the unbinding event probability between nanoparticles tethered to an atomic force microscopy tip and cells to the nanoparticle vectoring capacity. This novel approach allows for a rapid and cost-effective design of targeted nanomedicines reducing the need for long and tedious in vitro tests.
关键词： Targeted nanoparticles,Tailored nanomedicine,Tip functionalization,Single molecule force spectroscopy,Drug delivery
更新于2025-09-09 09:28:46
-
Real-time parallel 3D multiple particle tracking with single molecule centrifugal force microscopy
摘要： Real-time tracking of multiple particles is key for quantitative analysis of dynamic biophysical processes and materials science via time-lapse microscopy image data, especially for single molecule biophysical techniques, such as magnetic tweezers and centrifugal force microscopy. However, real-time multiple particle tracking with high resolution is limited by the current imaging processes or tracking algorithms. Here, we demonstrate 1 nm resolution in three dimensions in real-time with a graphics-processing unit (GPU) based on a compute unified device architecture (CUDA) parallel computing framework instead of only a central processing unit (CPU). We also explore the trade-offs between processing speed and size of the utilized regions of interest and a maximum speedup of 137 is achieved with the GPU compared with the CPU. Moreover, we utilize this method with our recently self-built centrifugal force microscope (CFM) in experiments that track multiple DNA-tethered particles. Our approach paves the way for high-throughput single molecule techniques with high resolution and efficiency.
关键词： image processing,single molecule force spectroscopy,GPU,particle tracking
更新于2025-09-09 09:28:46
-
Quantifying the Initial Unfolding of Bacteriorhodopsin Reveals Retinal Stabilization
摘要： The forces that stabilize membrane proteins remain elusive to precise quantification. Particularly important but poorly resolved are the forces present during a membrane protein’s initial unfolding, where the most native set of interactions are present. We developed a high-precision, atomic force microscopy assay to study the initial unfolding of bacteriorhodopsin. We discovered rapid near-equilibrium folding between the first three unfolding states that corresponded to the unfolding of 5 and 8 amino-acids respectively when using a cantilever optimized for 2-μs resolution. Interestingly, the third of these states was retinal stabilized and previously undetected despite being the most mechanically stable state in the whole unfolding pathway, supporting 150 pN for >1 min. We expect that this ability to measure the rapid and reversible dynamics in the initial unfolding of bacteriorhodopsin provides a platform for quantifying the energetics of membrane proteins under native-like conditions.
关键词： protein folding,single molecule force spectroscopy,site-specific bioconjugation,membrane proteins,atomic force microscopy
更新于2025-09-04 15:30:14