Exploring transduction mechanisms of protein transduction domains (PTDs) in living cells utilizing single-quantum dot tracking (SQT) technology (Q37988482)

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scientific article published on 05 January 2012

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English	Exploring transduction mechanisms of protein transduction domains (PTDs) in living cells utilizing single-quantum dot tracking (SQT) technology	scientific article published on 05 January 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

26 August 2017

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1 October 2019

Exploring transduction mechanisms of protein transduction domains (PTDs) in living cells utilizing single-quantum dot tracking (SQT) technology (English)

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Europe PubMed Central

PMC publication ID

26 August 2017

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manufactured product

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1 October 2019

author name string

Yasuhiro Suzuki

1

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Europe PubMed Central

PMC publication ID

26 August 2017

language of work or name

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publication date

5 January 2012

3 references

Europe PubMed Central

PMC publication ID

26 August 2017

1 October 2019

1 May 2020

3 references

Europe PubMed Central

PMC publication ID

26 August 2017

1 October 2019

1 May 2020

12

1 reference

Europe PubMed Central

PMC publication ID

26 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

26 August 2017

549-572

1 reference

Europe PubMed Central

PMC publication ID

26 August 2017

copyright license

Creative Commons Attribution

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1 October 2019

1 May 2020

copyright status

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Recent advances in protein transduction technology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3279229

6 September 2017

Delivering quantum dots to cells: bioconjugated quantum dots for targeted and nonspecific extracellular and intracellular imaging

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Probing cellular events, one quantum dot at a time

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Arginine-rich cell-penetrating peptides.

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Non-blinking semiconductor nanocrystals

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Advances in single-molecule fluorescence methods for molecular biology

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Molecular dynamics simulations suggest a mechanism for translocation of the HIV-1 TAT peptide across lipid membranes

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Dynamic recruitment of phospholipase C gamma at transiently immobilized GPI-anchored receptor clusters induces IP3-Ca2+ signaling: single-molecule tracking study 2

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GPI-anchored receptor clusters transiently recruit Lyn and G alpha for temporary cluster immobilization and Lyn activation: single-molecule tracking study 1

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Transcellular protein transduction using the Tat protein of HIV-1.

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Quantum dots for live cells, in vivo imaging, and diagnostics

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Interaction of the protein transduction domain of HIV-1 TAT with heparan sulfate: binding mechanism and thermodynamic parameters

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A brief introduction to cell-penetrating peptides

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Protein transduction domains of HIV-1 and SIV TAT interact with charged lipid vesicles. Binding mechanism and thermodynamic analysis

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Nuclear targeting of macromolecular polyanions by an HIV-Tat derived peptide. Role for cell-surface proteoglycans.

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Heparin binding by the HIV-1 tat protein transduction domain

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Molecular diversity of heparan sulfate

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TAT peptide on the surface of liposomes affords their efficient intracellular delivery even at low temperature and in the presence of metabolic inhibitors

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Selective CXCR4 antagonism by Tat: implications for in vivo expansion of coreceptor use by HIV-1

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Internalization of HIV-1 tat requires cell surface heparan sulfate proteoglycans

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Tat-mediated delivery of heterologous proteins into cells

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Autonomous functional domains of chemically synthesized human immunodeficiency virus tat trans-activator protein

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Endocytosis and targeting of exogenous HIV-1 Tat protein

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1 reference

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Identifiers

10.3390/S120100549

1 reference

Europe PubMed Central

PMC publication ID

26 August 2017

DBLP publication ID

journals/sensors/Suzuki12

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

26 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

26 August 2017

ResearchGate publication ID

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