Synthesis, structures and magnetism of a series of dinuclear and one-dimensional Ni–Ln complexes: single-molecule magnetic behavior in one-dimensional nitrate-bridged Dy analogue

2015 ◽  
Vol 39 (11) ◽  
pp. 8356-8363 ◽  
Author(s):  
Min-Xia Yao ◽  
Xing-Yun Lu ◽  
Zhao-Xia Zhu ◽  
Xiao-Wei Deng ◽  
Su Jing

By using a salen-type ligand and changing the reaction solvent, a series of NiII–LnIII complexes have been obtained and structurally and magnetically characterized.

2021 ◽  
Vol 22 (5) ◽  
pp. 2398
Author(s):  
Wooyoung Kang ◽  
Seungha Hwang ◽  
Jin Young Kang ◽  
Changwon Kang ◽  
Sungchul Hohng

Two different molecular mechanisms, sliding and hopping, are employed by DNA-binding proteins for their one-dimensional facilitated diffusion on nonspecific DNA regions until reaching their specific target sequences. While it has been controversial whether RNA polymerases (RNAPs) use one-dimensional diffusion in targeting their promoters for transcription initiation, two recent single-molecule studies discovered that post-terminational RNAPs use one-dimensional diffusion for their reinitiation on the same DNA molecules. Escherichia coli RNAP, after synthesizing and releasing product RNA at intrinsic termination, mostly remains bound on DNA and diffuses in both forward and backward directions for recycling, which facilitates reinitiation on nearby promoters. However, it has remained unsolved which mechanism of one-dimensional diffusion is employed by recycling RNAP between termination and reinitiation. Single-molecule fluorescence measurements in this study reveal that post-terminational RNAPs undergo hopping diffusion during recycling on DNA, as their one-dimensional diffusion coefficients increase with rising salt concentrations. We additionally find that reinitiation can occur on promoters positioned in sense and antisense orientations with comparable efficiencies, so reinitiation efficiency depends primarily on distance rather than direction of recycling diffusion. This additional finding confirms that orientation change or flipping of RNAP with respect to DNA efficiently occurs as expected from hopping diffusion.


2014 ◽  
Vol 53 (6) ◽  
pp. 2976-2982 ◽  
Author(s):  
Felix J. Klinke ◽  
Animesh Das ◽  
Serhiy Demeshko ◽  
Sebastian Dechert ◽  
Franc Meyer

1986 ◽  
Vol 108 (3) ◽  
pp. 368-371 ◽  
Author(s):  
Tadashi. Sugawara ◽  
Shunji. Bandow ◽  
Keisaku. Kimura ◽  
Hiizu. Iwamura ◽  
Koichi. Itoh

2017 ◽  
Vol 2017 (41) ◽  
pp. 4879-4883 ◽  
Author(s):  
Haitao Han ◽  
Xiao-Lei Li ◽  
Xiaofei Zhu ◽  
Guoshuai Zhang ◽  
Xinxin Hang ◽  
...  

1980 ◽  
Vol 34 (8) ◽  
pp. 667-670 ◽  
Author(s):  
J.C. Schouten ◽  
H. Hadders ◽  
K. Kopinga ◽  
W.J.M. de Jonge

Biomolecules ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 23 ◽  
Author(s):  
Dhawal Choudhary ◽  
Alessandro Mossa ◽  
Milind Jadhav ◽  
Ciro Cecconi

In the past three decades, the ability to optically manipulate biomolecules has spurred a new era of medical and biophysical research. Optical tweezers (OT) have enabled experimenters to trap, sort, and probe cells, as well as discern the structural dynamics of proteins and nucleic acids at single molecule level. The steady improvement in OT’s resolving power has progressively pushed the envelope of their applications; there are, however, some inherent limitations that are prompting researchers to look for alternatives to the conventional techniques. To begin with, OT are restricted by their one-dimensional approach, which makes it difficult to conjure an exhaustive three-dimensional picture of biological systems. The high-intensity trapping laser can damage biological samples, a fact that restricts the feasibility of in vivo applications. Finally, direct manipulation of biological matter at nanometer scale remains a significant challenge for conventional OT. A significant amount of literature has been dedicated in the last 10 years to address the aforementioned shortcomings. Innovations in laser technology and advances in various other spheres of applied physics have been capitalized upon to evolve the next generation OT systems. In this review, we elucidate a few of these developments, with particular focus on their biological applications. The manipulation of nanoscopic objects has been achieved by means of plasmonic optical tweezers (POT), which utilize localized surface plasmons to generate optical traps with enhanced trapping potential, and photonic crystal optical tweezers (PhC OT), which attain the same goal by employing different photonic crystal geometries. Femtosecond optical tweezers (fs OT), constructed by replacing the continuous wave (cw) laser source with a femtosecond laser, promise to greatly reduce the damage to living samples. Finally, one way to transcend the one-dimensional nature of the data gained by OT is to couple them to the other large family of single molecule tools, i.e., fluorescence-based imaging techniques. We discuss the distinct advantages of the aforementioned techniques as well as the alternative experimental perspective they provide in comparison to conventional OT.


RSC Advances ◽  
2015 ◽  
Vol 5 (67) ◽  
pp. 54403-54411 ◽  
Author(s):  
Krishanu Ray ◽  
Ramachandram Badugu ◽  
Joseph R. Lakowicz

Single particle fluorescence studies demonstrate increased brightness and reduced emission lifetime of individual QD575 on one-dimensional photonic crystal substrate.


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