15n-labeled Proteins

15N-labeled proteins are proteins containing the stable nitrogen isotope 15N instead of, or in addition to, naturally abundant 14N, enabling researchers to track nitrogen-containing residues with analytical methods. They are typically produced by expressing recombinant proteins in microorganisms grown on 15N-enriched media, allowing the isotope to become incorporated during biosynthesis. This labeling supports protein characterization by nuclear magnetic resonance spectroscopy, including 15N-1H correlation experiments, and by mass spectrometry. Researchers use 15N-labeled proteins to examine three-dimensional structure, folding, molecular interactions, conformational changes, and dynamics, making them valuable tools in biochemistry, structural biology, and biological technique development.

15n-labeled Proteins - Related Videos

Research

JoVE Journal - Immunology and Infection

Antibody Labeling with Fluorescent Dyes Using Magnetic Protein A and Protein G Beads

0 Views •

Cited by 3 •

2016

The on-bead method for labeling antibodies with small molecules enables labeling of a small amount of antibodies directly from cell media. This method is compatible with amine and thiol chemistry, and can handle multiple samples in parallel, manually or using automated platforms.

Research

JoVE Journal - Biology
Free Sample

Live Imaging of GFP-labeled Proteins in Drosophila Oocytes

0 Views •

Cited by 5 •

2013

A protocol for live imaging of GFP-tagged proteins or autofluorescent structures in individual Drosophila oocytes is described.

PIP-on-a-chip: A Label-free Study of Protein-phosphoinositide Interactions

0 Views •

Cited by 7 •

2017

Here we present a supported lipid bilayer in the context of a microfluidic platform to study protein-phosphoinositide interactions using a label-free method based on pH modulation.

Quantitative Flow Cytometry to Study Labeled Protein-Phospholipid Vesicle Interactions

0 Views •

2025

In this video, we demonstrate the interaction between proteins and artificial phospholipid vesicles using quantitative flow cytometry. The binding of fluorescently-labeled proteins to fluorescently-labeled phospholipid vesicles increases the mean fluorescence intensity, and this increase is detected by a flow cytometer.

AirID-Based Proximity Labeling for Protein-Protein Interaction in Plants

0 Views •

Cited by 1 •

2022

Here, we present a step-by-step protocol for performing the proximity labeling (PL) experiment in cucumber (Cucumis sativus L.) using AT4G18020 (APRR2)-AirID protein as a model. The method describes the construction of a vector, the transformation of a construct through agroinfiltration, biotin infiltration, protein extraction, and purification of biotin-labeled proteins through affinity purification technique.

View All Results

FAQs

Related Topics