Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

1.9K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
1.9K
Protein Folding01:22

Protein Folding

112.4K
Overview
112.4K
Protein Folding01:25

Protein Folding

8.8K
Proteins are chains of amino acids linked together by peptide bonds. Upon synthesis, a protein folds into a three-dimensional conformation, critical to its biological function. Interactions between its constituent amino acids guide protein folding, and hence the protein structure is primarily dependent on its amino acid sequence.
Protein Structure Is Critical to Its Biological Function
Proteins perform a wide range of biological functions such as catalyzing chemical reactions, providing...
8.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Mechanism of BCDX2-mediated RAD51 nucleation on short ssDNA stretches and fork DNA.

Nucleic acids research·2024
Same author

Comparison of Sonographic Findings with Diagnostic Mammography.

Journal of Nepal Health Research Council·2024
Same author

3D modelling of cavity-free lasing in nitrogen plasma filaments.

Optics express·2023
Same author

Normal mitochondrial function in <i>Saccharomyces cerevisiae</i> has become dependent on inefficient splicing.

eLife·2018
Same author

Fluorogenic RNA Mango aptamers for imaging small non-coding RNAs in mammalian cells.

Nature communications·2018
Same author

Bulky Lesion Bypass Requires Dpo4 Binding in Distinct Conformations.

Scientific reports·2017
Same journal

Tracking Synthetic Adhesins on Bacterial Surfaces with Immunofluorescence Microscopy.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Post-Selection Methods for Analyzing mRNA Display Selections and Optimization of Hits.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

High-Performance Computing in Tandem Mass Spectrometry (MS/MS) Peptide Identification.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Engineering and Adapting Disulfide-Containing Proteins to Enable Intracellular Functionality.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

AI-Driven Protein Research: From Prediction to Design.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Methods for the In Vitro Selection of Protein and Peptide Libraries Using mRNA Display.

Methods in molecular biology (Clifton, N.J.)·2026
See all related articles

Related Experiment Video

Updated: May 6, 2026

Nanomanipulation of Single RNA Molecules by Optical Tweezers
06:59

Nanomanipulation of Single RNA Molecules by Optical Tweezers

Published on: August 20, 2014

14.5K

RNA folding dynamics using laser-assisted single-molecule refolding.

Bishnu Paudel1, David Rueda

  • 1Department of Medicine, Section of Virology, Imperial College, London, UK.

Methods in Molecular Biology (Clifton, N.J.)
|October 19, 2013
PubMed
Summary
This summary is machine-generated.

We present detailed protocols for Laser-assisted single-molecule refolding (LASR), a technique combining temperature-jump kinetics and single-molecule detection to study complex RNA folding pathways and misfolded intermediates.

More Related Videos

OaAEP1-Mediated Enzymatic Synthesis and Immobilization of Polymerized Protein for Single-Molecule Force Spectroscopy
08:34

OaAEP1-Mediated Enzymatic Synthesis and Immobilization of Polymerized Protein for Single-Molecule Force Spectroscopy

Published on: February 5, 2020

6.1K
Thermodynamics of Membrane Protein Folding Measured by Fluorescence Spectroscopy
10:09

Thermodynamics of Membrane Protein Folding Measured by Fluorescence Spectroscopy

Published on: April 28, 2011

17.5K

Related Experiment Videos

Last Updated: May 6, 2026

Nanomanipulation of Single RNA Molecules by Optical Tweezers
06:59

Nanomanipulation of Single RNA Molecules by Optical Tweezers

Published on: August 20, 2014

14.5K
OaAEP1-Mediated Enzymatic Synthesis and Immobilization of Polymerized Protein for Single-Molecule Force Spectroscopy
08:34

OaAEP1-Mediated Enzymatic Synthesis and Immobilization of Polymerized Protein for Single-Molecule Force Spectroscopy

Published on: February 5, 2020

6.1K
Thermodynamics of Membrane Protein Folding Measured by Fluorescence Spectroscopy
10:09

Thermodynamics of Membrane Protein Folding Measured by Fluorescence Spectroscopy

Published on: April 28, 2011

17.5K

Area of Science:

  • Biochemistry and Molecular Biology
  • Biophysics

Background:

  • RNA folding pathways are complex, often involving kinetic traps and slow-to-resolve misfolded intermediates.
  • Understanding these pathways is crucial for elucidating RNA molecule biological functions.

Purpose of the Study:

  • To provide detailed protocols for performing Laser-assisted single-molecule refolding (LASR) experiments.
  • To enable researchers to characterize complex RNA folding pathways and misfolded intermediates.

Main Methods:

  • Laser-assisted single-molecule refolding (LASR) combines temperature-jump (T-jump) kinetics with single-molecule detection.
  • Single-molecule fluorescence resonance energy transfer (smFRET) is used to characterize conformational dynamics in real-time.
  • Protocols cover sample preparation, temperature calibration, and data analysis for LASR experiments.

Main Results:

  • Detailed protocols for LASR experiments are provided.
  • The protocols facilitate the characterization of RNA conformational dynamics.
  • The methods allow for the study of kinetic traps and misfolded intermediates in RNA folding.

Conclusions:

  • The provided LASR protocols offer a robust method for investigating complex RNA folding dynamics.
  • This technique is valuable for understanding how RNA molecules achieve their functional states.
  • Researchers can now more effectively characterize misfolded RNA intermediates and folding pathways.