scholarly journals Monitoring G-quadruplex formation with DNA carriers and solid-state nanopores

2019 ◽  
Author(s):  
Filip Bošković ◽  
Jinbo Zhu ◽  
Kaikai Chen ◽  
Ulrich F. Keyser

ABSTRACTG-quadruplexes (Gq) are guanine-rich DNA structures formed by single-stranded DNA. They are of paramount significance to gene expression regulation, but also drug targets for cancer and human viruses. Current ensemble and single-molecule methods require fluorescent labels, which can affect Gq folding kinetics. Here we introduce, a single-molecule Gq nanopore assay (smGNA) to detect Gqs and kinetics of Gq formation. We use ~5 nm solid-state nanopores to detect various Gq structural variants attached to designed DNA carriers. Gqs can be identified by localizing their positions along designed DNA carriers establishing smGNA as a tool for Gq mapping. In addition, smGNA allows for discrimination of (un-)folded Gq structures, provides insights into single-molecule kinetics of G-quadruplex folding, and probes quadruplex-to-duplex structural transitions. smGNA can elucidate the formation of G-quadruplexes at the single-molecule level without labelling and has potential implications on the study of these structures both in single-stranded DNA and in genomic samples.

2017 ◽  
Vol 53 (2) ◽  
pp. 436-439 ◽  
Author(s):  
Jinglin Kong ◽  
Jinbo Zhu ◽  
Ulrich F. Keyser

A novel nanopore-DNA carrier method is demonstrated for SNP detection and following DNA strand displacement kinetics at the single molecule level.


2010 ◽  
Vol 39 (9) ◽  
pp. 1343-1350 ◽  
Author(s):  
A. C. Krüger ◽  
M. K. Raarup ◽  
M. M. Nielsen ◽  
M. Kristensen ◽  
F. Besenbacher ◽  
...  

Author(s):  
Ilina Bareja ◽  
Hugo Wioland ◽  
Miro Janco ◽  
Philip R. Nicovich ◽  
Antoine Jégou ◽  
...  

ABSTRACTTropomyosins regulate dynamics and functions of the actin cytoskeleton by forming long chains along the two strands of actin filaments that act as gatekeepers for the binding of other actin-binding proteins. The fundamental molecular interactions underlying the binding of tropomyosin to actin are still poorly understood. Using microfluidics and fluorescence microscopy, we observed the binding of fluorescently labelled tropomyosin isoform Tpm1.8 to unlabelled actin filaments in real time. This approach in conjunction with mathematical modeling enabled us to quantify the nucleation, assembly and disassembly kinetics of Tpm1.8 on single filaments and at the single molecule level. Our analysis suggests that Tpm1.8 decorates the two strands of the actin filament independently. Nucleation of a growing tropomyosin domain proceeds with high probability as soon as the first Tpm1.8 molecule is stabilised by the addition of a second molecule, ultimately leading to full decoration of the actin filament. In addition, Tpm1.8 domains are asymmetrical, with enhanced dynamics at the edge oriented towards the barbed end of the actin filament. The complete description of Tpm1.8 kinetics on actin filaments presented here provides molecular insight into actin-tropomyosin filament formation and the role of tropomyosins in regulating actin filament dynamics.


2019 ◽  
Vol 40 (16-17) ◽  
pp. 2117-2124 ◽  
Author(s):  
Wei Si ◽  
Haojie Yang ◽  
Jingjie Sha ◽  
Yin Zhang ◽  
Yunfei Chen

2018 ◽  
Vol 115 (33) ◽  
pp. 8346-8351 ◽  
Author(s):  
Xiang Li ◽  
Yu Jiang ◽  
Shaorong Chong ◽  
David R. Walt

In this paper, we report an example of the engineered expression of tetrameric β-galactosidase (β-gal) containing varying numbers of active monomers. Specifically, by combining wild-type and single-nucleotide polymorphism plasmids at varying ratios, tetrameric β-gal was expressed in vitro with one to four active monomers. The kinetics of individual enzyme molecules revealed four distinct populations, corresponding to the number of active monomers in the enzyme. Using single-molecule-level enzyme kinetics, we were able to measure an accurate in vitro mistranslation frequency (5.8 × 10−4 per base). In addition, we studied the kinetics of the mistranslated β-gal at the single-molecule level.


2020 ◽  
Vol 142 (30) ◽  
pp. 13201-13209
Author(s):  
Yi Xiao ◽  
Jaeyoung Hong ◽  
Xiao Wang ◽  
Tao Chen ◽  
Taeghwan Hyeon ◽  
...  

2020 ◽  
Vol 1 (8) ◽  
pp. 2908-2916 ◽  
Author(s):  
Rameshwar L. Kumawat ◽  
Biswarup Pathak

The TOC features a scheme of solid-state nanochannel-based DNA sequencing techniques. DNA nucleobases can be analyzed at the single-molecule level by adsorption on topologically extended line defects in the graphene-based electrode setup.


2019 ◽  
Vol 40 (16-17) ◽  
Author(s):  
Wei Si ◽  
Haojie Yang ◽  
Jingjie Sha ◽  
Yin Zhang ◽  
Yunfei Chen

Sign in / Sign up

Export Citation Format

Share Document