scholarly journals Light-Induced Self-Assembly: Silver-Nanowire-Based Interferometric Optical Tweezers for Enhanced Optical Trapping and Binding of Nanoparticles (Adv. Funct. Mater. 7/2019)

2019 ◽  
Vol 29 (7) ◽  
pp. 1970043 ◽  
Author(s):  
Fan Nan ◽  
Zijie Yan
Author(s):  
Thomas Quail ◽  
Stefan Golfier ◽  
Maria Elsner ◽  
Keisuke Ishihara ◽  
Vasanthanarayan Murugesan ◽  
...  

AbstractInteractions between liquids and surfaces generate forces1,2 that are crucial for many processes in biology, physics and engineering, including the motion of insects on the surface of water3, modulation of the material properties of spider silk4 and self-assembly of microstructures5. Recent studies have shown that cells assemble biomolecular condensates via phase separation6. In the nucleus, these condensates are thought to drive transcription7, heterochromatin formation8, nucleolus assembly9 and DNA repair10. Here we show that the interaction between liquid-like condensates and DNA generates forces that might play a role in bringing distant regulatory elements of DNA together, a key step in transcriptional regulation. We combine quantitative microscopy, in vitro reconstitution, optical tweezers and theory to show that the transcription factor FoxA1 mediates the condensation of a protein–DNA phase via a mesoscopic first-order phase transition. After nucleation, co-condensation forces drive growth of this phase by pulling non-condensed DNA. Altering the tension on the DNA strand enlarges or dissolves the condensates, revealing their mechanosensitive nature. These findings show that DNA condensation mediated by transcription factors could bring distant regions of DNA into close proximity, suggesting that this physical mechanism is a possible general regulatory principle for chromatin organization that may be relevant in vivo.


Author(s):  
Yuki Uenobo ◽  
Tatsuya Shoji ◽  
Ayaka Mototsuji ◽  
Sawa Komoto ◽  
Tatsuya Nagai ◽  
...  

1997 ◽  
Vol 43 (2) ◽  
pp. 379-383 ◽  
Author(s):  
Kristian Helmerson ◽  
Rani Kishore ◽  
William D Phillips ◽  
Howard H Weetall

Abstract We used optical tweezers (optical trapping technology) to measure the force required to separate antigen–antibody bonds. Under competitive-binding conditions, we used the force determination to detect and measure protein antigen concentrations as small as 1 fmol/L (10−15 mol/L).


Author(s):  
Hui Jia ◽  
Xiao Yang ◽  
Qing-Qiang Kong ◽  
Li-Jing Xie ◽  
Quan-Gui Guo ◽  
...  

A free-standing graphene oxide/Ag nanowire film with a dense sandwich-like structure was fabricated via vacuum-assisted self-assembly. The EMI SE is up to 62 dB when the thickness is merely 8 μm in 8–40 GHz. The corresponding specific SE (EMI SE/t) is up to 77 500 dB cm−1.


Carbon ◽  
2013 ◽  
Vol 58 ◽  
pp. 198-207 ◽  
Author(s):  
Hsi-Wen Tien ◽  
Sheng-Tsung Hsiao ◽  
Wei-Hao Liao ◽  
Yi-Hsiuan Yu ◽  
Fong-Chi Lin ◽  
...  

2010 ◽  
Vol 19 (02) ◽  
pp. 371-378 ◽  
Author(s):  
P. YOUPLAO ◽  
T. PHATTARAWORAMET ◽  
S. MITATHA ◽  
C. TEEKA ◽  
P. P. YUPAPIN

We propose a novel system of an optical trapping tool using a dark-bright soliton pulse-propagating within an add/drop optical filter. The multiplexing signals with different wavelengths of the dark soliton are controlled and amplified within the system. The dynamic behavior of dark bright soliton interaction is analyzed and described. The storage signal is controlled and tuned to be an optical probe which can be configured as the optical tweezer. The optical tweezer storage is embedded within the add/drop optical filter system. By using some suitable parameters, we found that the tweezers storage time of 1.2 ns is achieved. Therefore, the generated optical tweezers can be stored and amplified within the design system. In application, the optical tweezers can be stored and trapped light/atom, which can be transmitted and recovered by using the proposed system.


2002 ◽  
Vol 01 (05n06) ◽  
pp. 465-469 ◽  
Author(s):  
TOSHIMI SHIMIZU ◽  
GEORGE JOHN ◽  
AKIHIRO FUKAGAWA ◽  
KOHZO ITO ◽  
HIROSHI FRUSAWA

Self-assembling behavior of both a cardanol-appended glycolipid mixture and the fractionated four components has been examined in aqueous solutions. The cardanyl glucoside mixture differing in the degree of unsaturation in the hydrophobic chain was found to self-assemble in water to form open-ended nanotube structures with 10–15 nm inner diameters. The pure saturated homologue produced twisted helical ribbons through self-assembly, whereas the monoene derivative gave tubular structures. The rational control of helical and tubular morphologies has been achieved by a combinatorial approach through the binary self-assembly of the saturated and monoene derivatives. The flexural rigidity of a single lipid nanotube was first evaluated using optical tweezers manipulation and then compared with that of natural microtubules.


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