Evidence map›Paper›PMID 34884694›Full record

ArticleInternational journal of molecular sciences2021

LSSmScarlet, dCyRFP2s, dCyOFP2s and CRISPRed2s, Genetically Encoded Red Fluorescent Proteins with a Large Stokes Shift.

Oksana M Subach, Anna V Vlaskina, Yuliya K Agapova, Pavel V Dorovatovskii, Alena Y Nikolaeva, Olga I Ivashkina, Vladimir O Popov, Kiryl D Piatkevich, Maria G Khrenova, Tatiana A Smirnova and 2 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 2 countries.

Oksana M SubachComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Anna V VlaskinaComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Yuliya K AgapovaComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Pavel V DorovatovskiiComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Alena Y NikolaevaComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Olga I IvashkinaComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Vladimir O PopovComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Kiryl D PiatkevichSchool of Life Sciences, Westlake University, Hangzhou 310024, China.ORCID 0000-0002-7777-9468
Maria G KhrenovaBach Institute of Biochemistry, Research Centre of Biotechnology of the Russian Academy of Sciences, 119071 Moscow, Russia.ORCID 0000-0001-7117-3089
Tatiana A SmirnovaCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Russian Academy of Sciences, 119334 Moscow, Russia.ORCID 0000-0002-7575-8591
Konstantin M BoykoBach Institute of Biochemistry, Research Centre of Biotechnology of the Russian Academy of Sciences, 119071 Moscow, Russia.ORCID 0000-0001-8229-189X
Fedor V SubachComplex of NBICS Technologies, National Research Center "Kurchatov Institute", 123182 Moscow, Russia.ORCID 0000-0003-2720-7821
Kurchatov Institute · RULomonosov Moscow State University · RUA N Bach Institute of Biochemistry · RUInstitute of Gene Biology · RUWestlake University · CN

Funding

2020 BBRF Young Investigator Grant Kiryl D. Piatkevichan internal grant of the National Research Center Kurchatov Institute №1056 of 02.07.2020MRIC Funding 103536022023National Natural Science Foundation of China 32050410298RFBR grant № 20-015-00427Russian Foundation for Basic Research 18-29-13006Russian Foundation for Basic Research 19-04-00395Russian Science Foundation 21-74-20135start-up funding from the Foundation of Westlake University Kiryl D. Piatkevichthe Ministry of Science and Higher Education of the Russian Federation grant №075-15-2019-1661
6 · The paper itself

Abstract

Genetically encoded red fluorescent proteins with a large Stokes shift (LSSRFPs) can be efficiently co-excited with common green FPs both under single- and two-photon microscopy, thus enabling dual-color imaging using a single laser. Recent progress in protein development resulted in a great variety of novel LSSRFPs; however, the selection of the right LSSRFP for a given application is hampered by the lack of a side-by-side comparison of the LSSRFPs' performance. In this study, we employed rational design and random mutagenesis to convert conventional bright RFP mScarlet into LSSRFP, called LSSmScarlet, characterized by excitation/emission maxima at 470/598 nm. In addition, we utilized the previously reported LSSRFPs mCyRFP1, CyOFP1, and mCRISPRed as templates for directed molecular evolution to develop their optimized versions, called dCyRFP2s, dCyOFP2s and CRISPRed2s. We performed a quantitative assessment of the developed LSSRFPs and their precursors in vitro on purified proteins and compared their brightness at 488 nm excitation in the mammalian cells. The monomeric LSSmScarlet protein was successfully utilized for the confocal imaging of the structural proteins in live mammalian cells and multicolor confocal imaging in conjugation with other FPs. LSSmScarlet was successfully applied for dual-color two-photon imaging in live mammalian cells. We also solved the X-ray structure of the LSSmScarlet protein at the resolution of 1.4 Å that revealed a hydrogen bond network supporting excited-state proton transfer (ESPT). Quantum mechanics/molecular mechanics molecular dynamic simulations confirmed the ESPT mechanism of a large Stokes shift. Structure-guided mutagenesis revealed the role of R198 residue in ESPT that allowed us to generate a variant with improved pH stability. Finally, we showed that LSSmScarlet protein is not appropriate for STED microscopy as a consequence of LSSRed-to-Red photoconversion with high-power 775 nm depletion light.

Indexed as

Cloning, MolecularHeLa CellsHumansLuminescent AgentsLuminescent ProteinsMolecular Dynamics SimulationMolecular StructureRed Fluorescent ProteinLuminescent AgentsLuminescent ProteinsRed Fluorescent ProteinCRISPRed2sdCyOFP2sdCyRFP2sfluorescence imagingfluorescent proteingenetically encoded red fluorescent proteinslarge Stokes shiftLSSmScarletprotein engineeringred fluorescent

Identifiers

PMID34884694
PMCPMC8657457
OpenAlexW3214868139

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.