A Bright Monomeric Near-Infrared Fluorescent Protein with an Excitation Peak at 633 nm for Labeling Cellular Protein and Reporting Protein-Protein Interaction.

ACS Sens

Guangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology & Center for Biomedical Optics and Molecular Imaging & CAS Key Laboratory of Health Informatics, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.

Published: July 2022

AI Article Synopsis

  • Bright monomeric near-infrared fluorescent proteins (NIR-FPs) are valuable for labeling proteins and cells and monitoring molecular activities in living organisms, but current versions struggle with brightness under common laser excitation.
  • Researchers introduced a new NIR-FP called mIFP663, which shows enhanced brightness at 633 nm and performs 3-6 times better than similar proteins in cellular applications.
  • mIFP663 can label important cellular and viral proteins without interfering with their functions and has been used to develop improved systems to study protein interactions in live cells.

Article Abstract

Bright monomeric near-infrared fluorescent proteins (NIR-FPs) are useful as markers for labeling proteins and cells and as sensors for reporting molecular activities in living cells and organisms. However, current monomeric NIR-FPs are dim under excitation with common 633/635/640 nm lasers, limiting their broad use in cellular/subcellular level imaging. Here, we report a bright monomeric NIR-FP with maximum excitation at 633 nm, named mIFP663, engineered from pv phytochrome (BphP). mIFP663 has high molecular brightness with a large extinction coefficient (86,600 M cm) and a decent quantum yield (19.4%), and high cellular brightness that is 3-6 times greater than those of spectrally similar NIR-FPs in HEK293T cells in the presence of exogenous BV. Moreover, we demonstrate that mIFP663 is able to label critical cellular and viral proteins without perturbing subcellular localization and virus replication, respectively. Finally, with mIFP663, we engineer improved bimolecular fluorescence complementation (BiFC) and new bioluminescent resonance energy transfer (BRET) systems to detect protein-protein interactions in living cells.

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Source
http://dx.doi.org/10.1021/acssensors.2c00286DOI Listing

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