Literature DB >> 26962999

Photophysics of the LOV-Based Fluorescent Protein Variant iLOV-Q489K Determined by Simulation and Experiment.

Mehdi D Davari1, Benita Kopka2, Marcus Wingen2, Marco Bocola1, Thomas Drepper2, Karl-Erich Jaeger2,3, Ulrich Schwaneberg1,4, Ulrich Krauss2.   

Abstract

Light, oxygen, voltage (LOV) based fluorescent proteins (FPs) represent a promising alternative to fluorescent reporters of the green fluorescent protein family. For certain applications like multicolor imaging or the design of FRET-based biosensors, the generation of spectrally shifted LOV-based FPs would be required. In a recent theoretical study ( Khrenova J. Phys. Chem. B 2015 , 119 ( 16 ), pp 5176 - 5183 ), the photophysical properties of a variant of the LOV-based fluorescent protein iLOV were predicted using quantum mechanics/molecular mechanics (QM/MM) approaches. The variant contained a lysine residue at the position of a highly conserved glutamine residue (Q489K), which directly interacts with the O4 and N5 atom of the flavin mononucleotide (FMN) chromophore. On the basis of QM/MM calculations, iLOV-Q489K was suggested to possess substantially red-shifted absorption and fluorescence-emission maxima with respect to parental iLOV. Here, we describe the experimental characterization of this variant, which, surprisingly contrary to the theoretical prediction, shows blue-shifted absorption and fluorescence-emission maxima. Using molecular dynamics (MD) simulations and QM/MM calculations, the molecular basis for the contradictory theoretical and experimental results is presented. Essentially, our computational analysis suggests that, in the Q489K variant, two possible side-chain conformers exist: (i) a least populated conformer K489in forming a hydrogen bond with the O4 atom of FMN chromophore and (ii) a most populated conformer K489out with the side-chain amino group flipped away from the FMN chromophore forming a new hydrogen bond with the backbone oxygen of G487. QM/MM calculated spectra of the K489out conformer are blue-shifted compared to the calculated spectra of parental iLOV, which is in accordance with experimental data. This suggests that the change in the conformation of K489 from K498in to K489out accounts for the change in the direction of the spectral shift from red to blue, thus reconciling theory and experiment.

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Year:  2016        PMID: 26962999     DOI: 10.1021/acs.jpcb.6b01512

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  9 in total

Review 1.  Blue-Light Receptors for Optogenetics.

Authors:  Aba Losi; Kevin H Gardner; Andreas Möglich
Journal:  Chem Rev       Date:  2018-07-09       Impact factor: 60.622

2.  Experimental Characterization of In Silico Red-Shift-Predicted iLOVL470T/Q489K and iLOVV392K/F410V/A426S Mutants.

Authors:  Pierre Wehler; Daniel Armbruster; Andreas Günter; Erik Schleicher; Barbara Di Ventura; Mehmet Ali Öztürk
Journal:  ACS Omega       Date:  2022-06-01

3.  Insertion position as well as the inserted TRS and gene sequences differentially affect the retention of foreign gene expression by simian hemorrhagic fever virus (SHFV).

Authors:  Han Di; Esther K Morantz; Heena Sadhwani; Joseph C Madden; Margo A Brinton
Journal:  Virology       Date:  2018-10-01       Impact factor: 3.616

Review 4.  Beyond the Green Fluorescent Protein: Biomolecular Reporters for Anaerobic and Deep-Tissue Imaging.

Authors:  Harun F Ozbakir; Nolan T Anderson; Kang-Ching Fan; Arnab Mukherjee
Journal:  Bioconjug Chem       Date:  2019-12-23       Impact factor: 4.774

5.  The molecular basis of spectral tuning in blue- and red-shifted flavin-binding fluorescent proteins.

Authors:  Katrin Röllen; Joachim Granzin; Alina Remeeva; Mehdi D Davari; Thomas Gensch; Vera V Nazarenko; Kirill Kovalev; Andrey Bogorodskiy; Valentin Borshchevskiy; Stefanie Hemmer; Ulrich Schwaneberg; Valentin Gordeliy; Karl-Erich Jaeger; Renu Batra-Safferling; Ivan Gushchin; Ulrich Krauss
Journal:  J Biol Chem       Date:  2021-04-13       Impact factor: 5.157

6.  Electron transfer pathways in a light, oxygen, voltage (LOV) protein devoid of the photoactive cysteine.

Authors:  Benita Kopka; Kathrin Magerl; Anton Savitsky; Mehdi D Davari; Katrin Röllen; Marco Bocola; Bernhard Dick; Ulrich Schwaneberg; Karl-Erich Jaeger; Ulrich Krauss
Journal:  Sci Rep       Date:  2017-10-17       Impact factor: 4.379

7.  Computational Investigation of Structural and Spectroscopic Properties of LOV-Based Proteins with Improved Fluorescence.

Authors:  Felipe Cardoso Ramos; Lorenzo Cupellini; Benedetta Mennucci
Journal:  J Phys Chem B       Date:  2021-02-10       Impact factor: 2.991

8.  Probing the Electron Transfer between iLOV Protein and Ag Nanoparticles.

Authors:  Xia Ran; Qianqian Zhang; Yu Zhang; Jin Chen; Zhongran Wei; Yulu He; Lijun Guo
Journal:  Molecules       Date:  2020-05-29       Impact factor: 4.411

9.  An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria.

Authors:  Stephan Endres; Marcus Wingen; Joaquim Torra; Rubén Ruiz-González; Tino Polen; Gabriela Bosio; Nora Lisa Bitzenhofer; Fabienne Hilgers; Thomas Gensch; Santi Nonell; Karl-Erich Jaeger; Thomas Drepper
Journal:  Sci Rep       Date:  2018-10-09       Impact factor: 4.379

  9 in total

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