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NanoFAST: structure-based design of a small fluorogen-activating protein with only 98 amino acids.

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TLDR
The shortened FAST is designed, which is composed of only 98 amino acids, the shortest genetically encoded tag among all known fluorescent and fluorogen-activating proteins, by truncating 26 N-terminal residues.
Abstract
One of the essential characteristics of any tag used in bioscience and medical applications is its size. The larger the label, the more it may affect the studied object, and the more it may distort its behavior. In this paper, using NMR spectroscopy and X-ray crystallography, we have studied the structure of fluorogen-activating protein FAST both in the apo form and in complex with the fluorogen. We showed that significant change in the protein occurs upon interaction with the ligand. While the protein is completely ordered in the complex, its apo form is characterized by higher mobility and disordering of its N-terminus. We used structural information to design the shortened FAST (which we named nanoFAST) by truncating 26 N-terminal residues. Thus, we created the shortest genetically encoded tag among all known fluorescent and fluorogen-activating proteins, which is composed of only 98 amino acids.

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Multifunctional stimuli-responsive chemogenetic platform for conditional multicolor cell-selective labeling

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Beyond DNA: new probes for PAINT super-resolution microscopy

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Fluorescence-Activating and Absorption-Shifting Tags for Advanced Imaging and Biosensing.

TL;DR: This Account presents the growing toolbox of fluorescence-activating and absorption-shifting tags (FASTs), small monomeric proteins of 14 kDa (125 amino acids residues) that can be used as markers to monitor gene expression and protein localization in live cells and organisms.
References
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Journal ArticleDOI

HaloTag: A Novel Protein Labeling Technology for Cell Imaging and Protein Analysis

TL;DR: The utility of this modular protein tagging system for cellular imaging and protein immobilization is demonstrated by analyzing multiple molecular processes associated with NF-kappaB-mediated cellular physiology, including imaging of subcellular protein translocation and capture of protein--protein and protein--DNA complexes.
Journal ArticleDOI

A general method for the covalent labeling of fusion proteins with small molecules in vivo

TL;DR: A general method for the covalent labeling of fusion proteins in vivo that complements existing methods for noncovalentlabeling of proteins and that may open up new ways of studying proteins in living cells is described.
Journal ArticleDOI

Fluorescent Proteins and Their Applications in Imaging Living Cells and Tissues

TL;DR: The structure, evolution, and function of GFP-like proteins and their numerous applications for in vivo imaging are focused on, with particular attention to recent techniques.
Journal ArticleDOI

RNA Mimics of Green Fluorescent Protein

TL;DR: The generation of RNA aptamers that bind fluorophores resembling the fluorophore in GFP provide an approach for genetic encoding of fluorescent RNAs and create a palette that spans the visible spectrum.
Journal ArticleDOI

A bright monomeric green fluorescent protein derived from Branchiostoma lanceolatum.

TL;DR: In this article, a monomeric yellow green fluorescent protein, mNeonGreen, derived from a tetrameric fluorescent protein from the cephalochordate Branchiostoma lanceolatum, was described.
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