Using nanoBRET and CRISPR/Cas9 to monitor proximity to a genome-edited protein in real-time
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Using nanoBRET and CRISPR/Cas9 to monitor proximity to a genome-edited protein in real-time
Authors
Keywords
-
Journal
Scientific Reports
Volume 7, Issue 1, Pages -
Publisher
Springer Nature
Online
2017-06-05
DOI
10.1038/s41598-017-03486-2
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- CXCR4 signaling is controlled by immobilization at the plasma membrane
- (2016) Elena Beletkaia et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- Targeted Elimination of G Proteins and Arrestins Defines Their Specific Contributions to Both Intensity and Duration of G Protein-coupled Receptor Signaling
- (2016) Elisa Alvarez-Curto et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The β-Arrestins: Multifunctional Regulators of G Protein-coupled Receptors
- (2016) Jeffrey S. Smith et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mutations of Vasopressin Receptor 2 Including Novel L312S Have Differential Effects on Trafficking
- (2016) Anatoly Tiulpakov et al. MOLECULAR ENDOCRINOLOGY
- The conformational signature of β-arrestin2 predicts its trafficking and signalling functions
- (2016) Mi-Hye Lee et al. NATURE
- β-Arrestin biosensors reveal a rapid, receptor-dependent activation/deactivation cycle
- (2016) Susanne Nuber et al. NATURE
- Versatile protein tagging in cells with split fluorescent protein
- (2016) Daichi Kamiyama et al. Nature Communications
- Monitoring G protein-coupled receptor and β-arrestin trafficking in live cells using enhanced bystander BRET
- (2016) Yoon Namkung et al. Nature Communications
- A simple method to generate stable cell lines for the analysis of transient protein-protein interactions
- (2016) Emilia Elizabeth Savage et al. BIOTECHNIQUES
- Fast and high resolution single-cell BRET imaging
- (2016) Elise Goyet et al. Scientific Reports
- NanoBRET—A Novel BRET Platform for the Analysis of Protein–Protein Interactions
- (2015) Thomas Machleidt et al. ACS Chemical Biology
- Self-Assembling NanoLuc Luciferase Fragments as Probes for Protein Aggregation in Living Cells
- (2015) Jia Zhao et al. ACS Chemical Biology
- Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System
- (2015) Bernd Zetsche et al. CELL
- Application of BRET to monitor ligand binding to GPCRs
- (2015) Leigh A Stoddart et al. NATURE METHODS
- Generation of knock-in primary human T cells using Cas9 ribonucleoproteins
- (2015) Kathrin Schumann et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Target engagement and drug residence time can be observed in living cells with BRET
- (2015) Matthew B. Robers et al. Nature Communications
- A generic strategy for CRISPR-Cas9-mediated gene tagging
- (2015) Daniel H. Lackner et al. Nature Communications
- CXCR4 over-expression and survival in cancer: A system review and meta-analysis
- (2015) Hongli Zhao et al. Oncotarget
- Rapid generation of endogenously driven transcriptional reporters in cells through CRISPR/Cas9
- (2015) Alejandro Rojas-Fernandez et al. Scientific Reports
- Genome editing of CXCR4 by CRISPR/cas9 confers cells resistant to HIV-1 infection
- (2015) Panpan Hou et al. Scientific Reports
- CRISPR/Cas9-mediated endogenous protein tagging for RESOLFT super-resolution microscopy of living human cells
- (2015) Michael Ratz et al. Scientific Reports
- Efficient CRISPR-Cas9-Mediated Generation of Knockin Human Pluripotent Stem Cells Lacking Undesired Mutations at the Targeted Locus
- (2015) Florian T. Merkle et al. Cell Reports
- A Protein-Tagging System for Signal Amplification in Gene Expression and Fluorescence Imaging
- (2014) Marvin E. Tanenbaum et al. CELL
- Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9
- (2014) Pankaj K. Mandal et al. Cell Stem Cell
- Comparative assessment of fluorescent transgene methods for quantitative imaging in human cells
- (2014) Robert Mahen et al. MOLECULAR BIOLOGY OF THE CELL
- One-Step Generation of Mice Carrying Reporter and Conditional Alleles by CRISPR/Cas-Mediated Genome Engineering
- (2013) Hui Yang et al. CELL
- DNA repair mechanisms in dividing and non-dividing cells
- (2013) Teruaki Iyama et al. DNA REPAIR
- The Bile Acid Receptor TGR5 Does Not Interact with β-Arrestins or Traffic to Endosomes but Transmits Sustained Signals from Plasma Membrane Rafts
- (2013) Dane D. Jensen et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Conformational biosensors reveal GPCR signalling from endosomes
- (2013) Roshanak Irannejad et al. NATURE
- DNA targeting specificity of RNA-guided Cas9 nucleases
- (2013) Patrick D Hsu et al. NATURE BIOTECHNOLOGY
- The transience of transient overexpression
- (2013) Toby J Gibson et al. NATURE METHODS
- Genome engineering using the CRISPR-Cas9 system
- (2013) F Ann Ran et al. Nature Protocols
- Multiplex Genome Engineering Using CRISPR/Cas Systems
- (2013) L. Cong et al. SCIENCE
- Engineered Luciferase Reporter from a Deep Sea Shrimp Utilizing a Novel Imidazopyrazinone Substrate
- (2012) Mary P. Hall et al. ACS Chemical Biology
- Effect of enhanced Renilla luciferase and fluorescent protein variants on the Förster distance of Bioluminescence resonance energy transfer (BRET)
- (2012) Helen Dacres et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Sensitive and High Resolution Localization and Tracking of Membrane Proteins in Live Cells with BRET
- (2012) Tien-Hung Lan et al. TRAFFIC
- Heteromerization of angiotensin receptors changes trafficking and arrestin recruitment profiles
- (2011) Enzo R. Porrello et al. CELLULAR SIGNALLING
- CXCR7/CXCR4 Heterodimer Constitutively Recruits β-Arrestin to Enhance Cell Migration
- (2011) Fabien M. Décaillot et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Efficient mutagenesis of the rhodopsin gene in rod photoreceptor neurons in mice
- (2011) Fung Chan et al. NUCLEIC ACIDS RESEARCH
- Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting
- (2011) Tomas Cermak et al. NUCLEIC ACIDS RESEARCH
- Internalization Dissociates β2-Adrenergic Receptors
- (2011) Tien-Hung Lan et al. PLoS One
- Application of G Protein-Coupled Receptor-Heteromer Identification Technology to Monitor β-Arrestin Recruitment to G Protein-Coupled Receptor Heteromers
- (2010) Heng B. See et al. ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES
- Multiplexing of Multicolor Bioluminescence Resonance Energy Transfer
- (2010) Billy Breton et al. BIOPHYSICAL JOURNAL
- Protein-protein interactions monitored in cells from transgenic mice using bioluminescence resonance energy transfer
- (2010) Martin Audet et al. FASEB JOURNAL
- Site-specific Phosphorylation of CXCR4 Is Dynamically Regulated by Multiple Kinases and Results in Differential Modulation of CXCR4 Signaling
- (2010) John M. Busillo et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- β2-Adrenergic Receptor Signaling in the Cardiac Myocyte is Modulated by Interactions With CXCR4
- (2010) Thomas J LaRocca et al. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
- Rab GTPases Bind at a Common Site within the Angiotensin II Type I Receptor Carboxyl-Terminal Tail: Evidence that Rab4 Regulates Receptor Phosphorylation, Desensitization, and Resensitization
- (2010) J. L. Esseltine et al. MOLECULAR PHARMACOLOGY
- CXCR7 heterodimerizes with CXCR4 and regulates CXCL12-mediated G protein signaling
- (2009) A. Levoye et al. BLOOD
- Agonist-Independent Interactions between β-Arrestins and Mutant Vasopressin Type II Receptors Associated with Nephrogenic Syndrome of Inappropriate Antidiuresis
- (2009) Martina Kocan et al. MOLECULAR ENDOCRINOLOGY
- Functional complementation of high-efficiency resonance energy transfer: a new tool for the study of protein binding interactions in living cells
- (2007) Paola Molinari et al. BIOCHEMICAL JOURNAL
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started