Bipartite Nls

A bipartite nuclear localization signal (NLS) is a protein-targeting sequence that directs cargo into the cell nucleus, where many processes such as gene regulation and DNA replication occur. It contains two clusters of basic amino acids, typically lysine or arginine residues, separated by a spacer region; importin-α recognizes the signal and, with importin-β, mediates transport through the nuclear pore complex. Bipartite NLSs help regulate the intracellular distribution and activity of transcription factors, signaling proteins, and other nuclear cargo. Identifying these motifs supports studies of protein localization, nuclear transport, and mechanisms of cellular regulation.

Bipartite Nls - Related Videos

Research

JoVE Journal - Bioengineering

Initial Evaluation of Antibody-conjugates Modified with Viral-derived Peptides for Increasing Cellular Accumulation and Improving Tumor Targeting

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Cited by 5 •

2018

Viral-derived peptides coupled to antibody-conjugates (ACs) is an approach gaining momentum due to the potential of delivering molecular payloads with increased tumor cell accumulation. Utilizing common methods to evaluate peptide conjugation, AC and payload intracellular accumulation, and tumor targeting, this protocol helps researchers during the key initial development phases.

Assays for the Degradation of Misfolded Proteins in Cells

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Cited by 5 •

2016

This report describes protocols for measuring degradation rates of misfolded proteins by either western blot or fluorescence-based assays. The methods can be applied to analysis of other misfolded proteins and for high throughput screening.

Evaluating the Intracellular Distribution of Virus-Derived Peptide-Modified Antibody Conjugates

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2025

This video demonstrates the process of assessing the intracellular distribution of virus-derived peptide-modified antibody conjugates using confocal microscopy. The viral-derived nuclear localization sequence directs antibody-conjugates within the cytoplasm, confirmed through immunostaining and fluorescence measurement.

Quantitative Analysis and Characterization of Atherosclerotic Lesions in the Murine Aortic Sinus

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Cited by 51 •

2013

We describe procedures to quantify and characterize atherosclerotic lesions in mouse models using precision sectioning of the aortic sinus and ascending aorta combined with histochemical and immunohistochemical analysis.

Measuring the Kinetics of mRNA Transcription in Single Living Cells

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Cited by 6 •

2011

RNA polymerase II transcriptional kinetics are measured on specific genes in living cells. mRNAs transcribed from the gene of interest are fluorescently tagged and using Fluorescence Recovery After Photobleaching (FRAP) the in vivo kinetics of transcriptional elongation are obtained.

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