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Technology Development Initiative – Paper of the Month – March 2024

A figure from this article - Image Copyright: Nature Methods

Image Copyright: Nature Methods

Adaptable, turn-on maturation (ATOM) fluorescent biosensors for multiplexed detection in cells

Published in Nature Methods (2023)

Authors

Harsimranjit Sekhon, Jeung-Hoi Ha, Maria F Presti, Spencer B Procopio, Ava R Jarvis, Paige O Mirsky, Anna M John, Stewart N Loh

Paper presented by Dr. Reinis Svarcbahs and selected by the NIDA TDI Paper of the Month Committee

Publication Brief Description

Turn-on fluorescent protein-based biosensors typically require long, painstaking engineering and cannot be easily adapted to different targets. In this paper, authors developed a single-molecule, turn-on maturation fluorescent protein-based platform that can be adapted to recognize different proteins of choice. These biosensors consist of a fluorescent protein and circularly permuted nanobody or monobody, named adaptable, turn-on maturation (ATOM) biosensors. Biosensors are based on an observation that a yellow fluorescent protein with a circularly permuted FK506-binding protein exhibited a 35-fold turn-on of yellow fluorescence with the addition of FK506 or its analog rapamycin. The authors furthered the approach by circularly permuting nanobodies and monobodies with cyan, yellow, and red fluorescent proteins. As a proof of concept, they generated circularly permuted monobody of human proteins hRAS, c-Abl Src homology 2 (SH2) domain and WD repeat-containing protein 5 (WDR5), and mCherry recognizing nanobody that are localized to different cell compartments. All sensors displayed up to 60-fold increase in fluorescence upon binding to the target in cells and more than 100-fold increase in vitro. Overall, the authors describe reagents to create a turn-on biosensor from a monobody or nanobody that recognizes your protein of interest.


Sekhon, Harsimranjit; Ha, Jeung-Hoi; Presti, Maria F; Procopio, Spencer B; Jarvis, Ava R; Mirsky, Paige O; John, Anna M; Loh, Stewart N

Adaptable, turn-on maturation (ATOM) fluorescent biosensors for multiplexed detection in cells Journal Article

In: Nat Methods, vol. 20, no. 12, pp. 1920–1929, 2023, ISSN: 1548-7105.

Abstract | Links

@article{pmid37945909,
title = {Adaptable, turn-on maturation (ATOM) fluorescent biosensors for multiplexed detection in cells},
author = {Harsimranjit Sekhon and Jeung-Hoi Ha and Maria F Presti and Spencer B Procopio and Ava R Jarvis and Paige O Mirsky and Anna M John and Stewart N Loh},
url = {https://pubmed.ncbi.nlm.nih.gov/37945909/},
doi = {10.1038/s41592-023-02065-w},
issn = {1548-7105},
year = {2023},
date = {2023-12-01},
urldate = {2023-12-01},
journal = {Nat Methods},
volume = {20},
number = {12},
pages = {1920--1929},
abstract = {A grand challenge in biosensor design is to develop a single-molecule, fluorescent protein-based platform that can be easily adapted to recognize targets of choice. Here, we created a family of adaptable, turn-on maturation (ATOM) biosensors consisting of a monobody (circularly permuted at one of two positions) or a nanobody (circularly permuted at one of three positions) inserted into a fluorescent protein at one of three surface loops. Multiplexed imaging of live human cells coexpressing cyan, yellow and red ATOM sensors detected biosensor targets that were specifically localized to various subcellular compartments. Fluorescence activation involved ligand-dependent chromophore maturation with turn-on ratios of up to 62-fold in cells and 100-fold in vitro. Endoplasmic reticulum- and mitochondria-localized ATOM sensors detected ligands that were targeted to those organelles. The ATOM design was validated with three monobodies and one nanobody inserted into distinct fluorescent proteins, suggesting that customized ATOM sensors can be generated quickly.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}

Close

A grand challenge in biosensor design is to develop a single-molecule, fluorescent protein-based platform that can be easily adapted to recognize targets of choice. Here, we created a family of adaptable, turn-on maturation (ATOM) biosensors consisting of a monobody (circularly permuted at one of two positions) or a nanobody (circularly permuted at one of three positions) inserted into a fluorescent protein at one of three surface loops. Multiplexed imaging of live human cells coexpressing cyan, yellow and red ATOM sensors detected biosensor targets that were specifically localized to various subcellular compartments. Fluorescence activation involved ligand-dependent chromophore maturation with turn-on ratios of up to 62-fold in cells and 100-fold in vitro. Endoplasmic reticulum- and mitochondria-localized ATOM sensors detected ligands that were targeted to those organelles. The ATOM design was validated with three monobodies and one nanobody inserted into distinct fluorescent proteins, suggesting that customized ATOM sensors can be generated quickly.

Close

  • https://pubmed.ncbi.nlm.nih.gov/37945909/
  • doi:10.1038/s41592-023-02065-w

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