Tuning Two-Photon Absorption in Rhodopsin Chromophore via Backbone Modification: The Story Told by CC2 and TD-DFT

We investigate here a systematic way to tune two-photon transition strengths (δ<sup>2PA</sup>) and two-photon absorption (2PA) cross sections (σ<sup>2PA</sup>) of the rhodopsin's chromophore 11-<i>cis</i>-retinal protonated Schiff base (RPSB) via the modulation of the methyl groups pattern along its polyene chain. Our team employed the resolution of identity, coupled cluster approximate second order (RI-CC2) method with Dunning's aug-cc-pVDZ basis set, to determine the structural impact on δ<sup>2PA</sup>, as well as its correlation to both transition dipole moments and permanent electric dipole moments. Seven structures were probed in vacuo, including five-double-bond-conjugated model of the native chromophore, shortened by the β-ionone ring (RPSB5), and its de/methylated analogues: 9-methyl, 13-methyl, planar and twisted models of 9,10-dimethyl and 9,10,13-trimethyl. Our results demonstrate that the magnitude of δ<sup>2PA</sup> is dictated by both the position and number of methylated groups attached to its polyene chain as well as the degree of dihedral twist that is introduced due to the de/methylation. In fact, a strong correlation between δ<sup>2PA</sup> enhancement and the presence of a C13-methyl group in the planar RPSB5 species is found. Trends in δ<sup>2PA</sup> values follow the trends observed in their corresponding changes in the permanent dipole moment upon the S0-S1 excitation nearly exactly. The assessment of four DFT functionals, i.e., M11, MN15, CAM-B3LYP, and BHandHLYP, previously found most successful in predicting 2PA properties in biological chromophores, points to a long-range-corrected hybrid meta-GGA M11 as the top-performing functional, albeit still delivering underestimated δ<sup>2PA</sup> and σ<sup>2PA</sup> values by a factor of 3.3-5.3 with respect to the CC2 results. In the case of global-hybrid meta-NGA (MN15), as well as CAM-B3LYP and BHandHLYP functionals, this factor deteriorates significantly to 6.7-20.9 and is mostly related to significantly lower quality of the ground- and excited-state dipole moments.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2024-09-13
DOI
https://doi.org/10.1021/acs.jctc.4c00675
Citations
2
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
0.54
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article

Tuning Two-Photon Absorption in Rhodopsin Chromophore via Backbone Modification: The Story Told by CC2 and TD-DFT

Saruti Sirimatayanant, Tadeusz Andruniów
2 citations
Journal of Chemical Theory and Computation
Photoreceptor and optogenetics research
0.54
article

Tuning Two-Photon Absorption in Rhodopsin Chromophore via Backbone Modification: The Story Told by CC2 and TD-DFT

Saruti Sirimatayanant, Tadeusz Andruniów
article en
2 citations

Abstract

We investigate here a systematic way to tune two-photon transition strengths (δ<sup>2PA</sup>) and two-photon absorption (2PA) cross sections (σ<sup>2PA</sup>) of the rhodopsin's chromophore 11-<i>cis</i>-retinal protonated Schiff base (RPSB) via the modulation of the methyl groups pattern along its polyene chain. Our team employed the resolution of identity, coupled cluster approximate second order (RI-CC2) method with Dunning's aug-cc-pVDZ basis set, to determine the structural impact on δ<sup>2PA</sup>, as well as its correlation to both transition dipole moments and permanent electric dipole moments. Seven structures were probed in vacuo, including five-double-bond-conjugated model of the native chromophore, shortened by the β-ionone ring (RPSB5), and its de/methylated analogues: 9-methyl, 13-methyl, planar and twisted models of 9,10-dimethyl and 9,10,13-trimethyl. Our results demonstrate that the magnitude of δ<sup>2PA</sup> is dictated by both the position and number of methylated groups attached to its polyene chain as well as the degree of dihedral twist that is introduced due to the de/methylation. In fact, a strong correlation between δ<sup>2PA</sup> enhancement and the presence of a C13-methyl group in the planar RPSB5 species is found. Trends in δ<sup>2PA</sup> values follow the trends observed in their corresponding changes in the permanent dipole moment upon the S0-S1 excitation nearly exactly. The assessment of four DFT functionals, i.e., M11, MN15, CAM-B3LYP, and BHandHLYP, previously found most successful in predicting 2PA properties in biological chromophores, points to a long-range-corrected hybrid meta-GGA M11 as the top-performing functional, albeit still delivering underestimated δ<sup>2PA</sup> and σ<sup>2PA</sup> values by a factor of 3.3-5.3 with respect to the CC2 results. In the case of global-hybrid meta-NGA (MN15), as well as CAM-B3LYP and BHandHLYP functionals, this factor deteriorates significantly to 6.7-20.9 and is mostly related to significantly lower quality of the ground- and excited-state dipole moments.

Journal of Chemical Theory and Computation
Wrocław University of Science and Technology (PL), AGH University of Krakow (PL)
Openalex Percentile: Top 35%
Photoreceptor and optogenetics research
0.54
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