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Photoswitching Proteins

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Cover of 'Photoswitching Proteins'

Table of Contents

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    Book Overview
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    Chapter 1 Photoinduced damage resulting from fluorescence imaging of live cells.
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    Chapter 2 Modification of purified proteins with photochemical protection compounds for high-resolution photoactivation of protein function in vitro and in vivo.
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    Chapter 3 Optochemical activation of kinase function in live cells.
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    Chapter 4 Photoswitching of cell surface receptors using tethered ligands.
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    Chapter 5 Photocontrol of AMPA receptors with a photochromic ligand.
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    Chapter 6 Photoconversion of CFP to Study Neuronal Tissue with Electron Microscopy.
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    Chapter 7 Light-inducible gene regulation with engineered zinc finger proteins.
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    Chapter 8 Manipulation of plasma membrane phosphoinositides using photoinduced protein-protein interactions.
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    Chapter 9 A roadmap to applying optogenetics in neuroscience.
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    Chapter 10 Salvaging ruins: reverting blind retinas into functional visual sensors.
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    Chapter 11 Photoactivated adenylyl cyclases as optogenetic modulators of neuronal activity.
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    Chapter 12 Structural basis of photoswitching in fluorescent proteins.
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    Chapter 13 Using Photoactivatable GFP to Track Axonal Transport Kinetics.
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    Chapter 14 In Vivo Cell Tracking Using PhOTO Zebrafish.
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    Chapter 15 In Vivo Optogenetics for Light-Induced Oxidative Stress in Transgenic Zebrafish Expressing the KillerRed Photosensitizer Protein.
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    Chapter 16 Photoactivatable Fluorescent Proteins for Super-resolution Microscopy.
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    Chapter 17 pcSOFI as a Smart Label-Based Superresolution Microscopy Technique.
Attention for Chapter 7: Light-inducible gene regulation with engineered zinc finger proteins.
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Chapter title
Light-inducible gene regulation with engineered zinc finger proteins.
Chapter number 7
Book title
Photoswitching Proteins
Published in
Methods in molecular biology, March 2014
DOI 10.1007/978-1-4939-0470-9_7
Pubmed ID
Book ISBNs
978-1-4939-0469-3, 978-1-4939-0470-9
Authors

Polstein LR, Gersbach CA, Lauren R. Polstein, Charles A. Gersbach Ph.D., Polstein, Lauren R., Gersbach, Charles A., Charles A. Gersbach

Editors

Sidney Cambridge

Abstract

The coupling of light-inducible protein-protein interactions with gene regulation systems has enabled the control of gene expression with light. In particular, heterodimer protein pairs from plants can be used to engineer a gene regulation system in mammalian cells that is reversible, repeatable, tunable, controllable in a spatiotemporal manner, and targetable to any DNA sequence. This system, Light-Inducible Transcription using Engineered Zinc finger proteins (LITEZ), is based on the blue light-induced interaction of GIGANTEA and the LOV domain of FKF1 that drives the localization of a transcriptional activator to the DNA-binding site of a highly customizable engineered zinc finger protein. This chapter provides methods for modifying LITEZ to target new DNA sequences, engineering a programmable LED array to illuminate cell cultures, and using the modified LITEZ system to achieve spatiotemporal control of transgene expression in mammalian cells.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Austria 1 4%
Unknown 26 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 19%
Researcher 3 11%
Student > Master 3 11%
Student > Bachelor 3 11%
Student > Doctoral Student 2 7%
Other 7 26%
Unknown 4 15%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 9 33%
Agricultural and Biological Sciences 8 30%
Unspecified 1 4%
Social Sciences 1 4%
Medicine and Dentistry 1 4%
Other 3 11%
Unknown 4 15%