Results 71 to 80 of about 5,402,175 (290)

USP29‐regulated noncanonical stabilization of the hypoxia‐inducible factor‐α in aggressive prostate cancer

open access: yesMolecular Oncology, EarlyView.
We identify USP29 as the only DUB mirroring CA9 expression, a marker of hypoxia and HIF pathway activation associated with PCA aggressiveness. USP29 stabilizes HIF‐1α and HIF‐2α via a noncanonical mechanism that is independent of PHD/pVHL activity yet relies on proteasomal regulation, establishing USP29 as a previously unrecognized regulator of hypoxic
Amelie S Schober   +16 more
wiley   +1 more source

Monitoring multiple distances within a single molecule using switchable FRET [PDF]

open access: yes, 2010
Uphoff S, Holden SJ, Le Reste L, et al. Monitoring multiple distances within a single molecule using switchable FRET. NATURE METHODS. 2010;7(10):831-836.The analysis of structure and dynamics of biomolecules is important for understanding their function.
Mike Heilemann   +21 more
core   +1 more source

ABCE1 Controls Ribosome Recycling by an Asymmetric Dynamic Conformational Equilibrium

open access: yesCell Reports, 2019
Summary: The twin-ATPase ABCE1 has a vital function in mRNA translation by recycling terminated or stalled ribosomes. As for other functionally distinct ATP-binding cassette (ABC) proteins, the mechanochemical coupling of ATP hydrolysis to conformational
Giorgos Gouridis   +7 more
doaj   +1 more source

Time-resolved burst variance analysis

open access: yesBiophysical Reports, 2023
Quantifying biomolecular dynamics has become a major task of single-molecule fluorescence spectroscopy methods. In single-molecule Förster resonance energy transfer (smFRET), kinetic information is extracted from the stream of photons emitted by attached
Ivan Terterov   +3 more
doaj   +1 more source

Single-molecule FRET measures bends and kinks in DNA [PDF]

open access: yesProceedings of the National Academy of Sciences, 2008
We present advances in the use of single-molecule FRET measurements with flexibly linked dyes to derive full 3D structures of DNA constructs based on absolute distances. The resolution obtained by this single-molecule approach harbours the potential to study in detail also protein- or damage-induced DNA bending.
Wozniak, Anna K.   +4 more
openaire   +4 more sources

Single‐molecule DNA flow‐stretch assays for high‐throughput DNA–protein interaction studies

open access: yesFEBS Open Bio, EarlyView.
We describe an optimised single‐molecule DNA flow‐stretch assay that visualises DNA–protein interactions in real time. Linear DNA fragments are tethered to a surface and stretched by buffer flow for fluorescence imaging. Using λ and φX174 DNA, this protocol enhances reproducibility and accessibility, providing a versatile approach for studying diverse ...
Ayush Kumar Ganguli   +8 more
wiley   +1 more source

Identification of binding mechanisms in single molecule-DNA complexes [PDF]

open access: yes, 2003
Eckel R, Ros R, Ros A, Wilking SD, Sewald N, Anselmetti D. Identification of binding mechanisms in single molecule-DNA complexes. Biophysical journal. 2003;85(3):1968-1973.Changes in the elastic properties of single deoxyribonucleic acid (DNA) molecules ...
Anselmetti, Dario   +14 more
core   +1 more source

ABEL-FRET: tether-free single-molecule FRET with hydrodynamic profiling

open access: yes, 2021
Raw Data related to the manuscript: "ABEL-FRET: tether-free single-molecule FRET with hydrodynamic profiling" Contains the following files: ReadMe.txt - a quick introduction to the upload ABEL-FRET-data-format-exampleCode.docx - a detailed ...
Wilson, Hugh, Wang, Quan
core   +1 more source

Optimal Background Estimators in Single-Molecule FRET Microscopy [PDF]

open access: yesBiophysical Journal, 2016
Single-molecule total internal reflection fluorescence (TIRF) microscopy constitutes an umbrella of powerful tools that facilitate direct observation of the biophysical properties, population heterogeneities, and interactions of single biomolecules without the need for ensemble synchronization.
Preus, Soren   +2 more
openaire   +3 more sources

Optimizing photoactivation of PA‐mCherry for optical pooled CRISPR screens

open access: yesFEBS Open Bio, EarlyView.
Photoactivatable PA‐mCherry finds widespread use to optically tag individual cells. However, confocal 405 nm UV laser‐scanning (normal scan) is much less efficient than widefield UV illumination, limiting the use of PA‐mCherry on confocal instruments. We remedy this limitation by reporting that rapid and repeated confocal scanning with a low‐intensity,
Sravasti Mukherjee   +3 more
wiley   +1 more source

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