Evidence map›Paper›PMID 34185946›Full record

ArticleChemphyschem : a European journal of chemical physics and physical chemistry2021

Molecular and Spectroscopic Characterization of Green and Red Cyanine Fluorophores from the Alexa Fluor and AF Series*.

Christian Gebhardt, Martin Lehmann, Maria M Reif, Martin Zacharias, Gerd Gemmecker, Thorben Cordes

Abstract read
In one paragraph

Article in Chemphyschem : a European journal of chemical physics and physical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

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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

6 authors.

Christian GebhardtPhysical and Synthetic Biology, Faculty of Biology, Ludwig-Maximilians-Universität München, Großhadernerstr. 2-4, 82152, Planegg-Martinsried, Germany.
Martin LehmannPlant Molecular Biology, Faculty of Biology, Ludwig-Maximilians-Universität München, Großhadernerstr. 2-4, 82152, Planegg-Martinsried, Germany.
Maria M ReifTheoretical Biophysics (T38), Physics Department, Technical University of Munich, Center for Functional Protein Assemblies (CPA), Ernst-Otto-Fischer-Str. 8, 85748, Garching, Germany.
Martin ZachariasTheoretical Biophysics (T38), Physics Department, Technical University of Munich, Center for Functional Protein Assemblies (CPA), Ernst-Otto-Fischer-Str. 8, 85748, Garching, Germany.
Gerd GemmeckerBavarian NMR Center (B NMRZ), Department of Chemistry, Technical University of Munich, Lichtenbergstr. 4, 85748, Garching, Germany.
Thorben CordesPhysical and Synthetic Biology, Faculty of Biology, Ludwig-Maximilians-Universität München, Großhadernerstr. 2-4, 82152, Planegg-Martinsried, Germany.ORCID 0000-0002-8598-5499

Funding

Bayerisches NMR-Zentrum (B NMRZ)Center for integrated protein science Munich (CiPSM)Center for Nanoscience (CeNS)Deutsche Forschungsgemeinschaft A10Deutsche Forschungsgemeinschaft A13Deutsche Forschungsgemeinschaft A13-111166240Deutsche Forschungsgemeinschaft C03Deutsche Forschungsgemeinschaft GRK2062Deutsche Forschungsgemeinschaft SFB863ERC ERC-StG 638536Helmholtz Zentrum für Gesundheit und UmweltRegionales Rechenzentrum Erlangen (RRZE)Studienstiftung des deutschen VolkesTU München
6 · The paper itself

Abstract

The use of fluorescence techniques has an enormous impact on various research fields including imaging, biochemical assays, DNA-sequencing and medical technologies. This has been facilitated by the development of numerous commercial dyes with optimized photophysical and chemical properties. Often, however, information about the chemical structures of dyes and the attached linkers used for bioconjugation remain a well-kept secret. This can lead to problems for research applications where knowledge of the dye structure is necessary to predict or understand (unwanted) dye-target interactions, or to establish structural models of the dye-target complex. Using a combination of optical spectroscopy, mass spectrometry, NMR spectroscopy and molecular dynamics simulations, we here investigate the molecular structures and spectroscopic properties of dyes from the Alexa Fluor (Alexa Fluor 555 and 647) and AF series (AF555, AF647, AFD647). Based on available data and published structures of the AF and Cy dyes, we propose a structure for Alexa Fluor 555 and refine that of AF555. We also resolve conflicting reports on the linker composition of Alexa Fluor 647 maleimide. We also conducted a comprehensive comparison between Alexa Fluor and AF dyes by continuous-wave absorption and emission spectroscopy, quantum yield determination, fluorescence lifetime and anisotropy spectroscopy of free and protein-attached dyes. All these data support the idea that Alexa Fluor and AF dyes have a cyanine core and are a derivative of Cy3 and Cy5. In addition, we compared Alexa Fluor 555 and Alexa Fluor 647 to their structural homologs AF555 and AF(D)647 in single-molecule FRET applications. Both pairs showed excellent performance in solution-based smFRET experiments using alternating laser excitation. Minor differences in apparent dye-protein interactions were investigated by molecular dynamics simulations. Our findings clearly demonstrate that the AF-fluorophores are an attractive alternative to Alexa- and Cy-dyes in smFRET studies or other fluorescence applications.

Indexed as

CarbocyaninesCysteineFluorescence PolarizationFluorescence Resonance Energy TransferFluorescent DyesMagnetic Resonance SpectroscopyMass SpectrometryMolecular Dynamics SimulationMolecular StructureProteinsRhodaminesSingle Molecule ImagingSulfonic AcidsAlexa Fluor 555Alexa Fluor 647Carbocyaninescyanine dye 3CysteineFluorescent DyesProteinsRhodaminesSulfonic AcidsAlexa dyesbiolabelingfluorescence spectroscopyFörster resonance energy transferorganic fluorophores

Identifiers

PMID34185946
PMCPMC8457111

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.