Examining the origins of observed terahertz modes from an optically pumped atomistic model protein in aqueous solution

被引:7
作者
Azizi, Khatereh [1 ,2 ]
Gori, Matteo [2 ]
Morzan, Uriel [1 ]
Hassanali, Ali [1 ]
Kurian, Philip [2 ]
机构
[1] Abdus Salam Int Ctr Theoret Phys, Str Costiera 11, I-34151 Trieste, Italy
[2] Howard Univ, Quantum Biol Lab, Washington, DC 20060 USA
来源
PNAS NEXUS | 2023年 / 2卷 / 08期
关键词
terahertz spectra; Frohlich condensates; bovine serum albumin (BSA) protein; molecular dynamics (MD) simulation; optomechanical transduction; DYNAMICAL HYDRATION SHELL; MOLECULAR-DYNAMICS; WATER; MOTIONS; TIME; CONDENSATION; EQUILIBRIUM; FLEXIBILITY; TRYPTOPHAN; SPECTRA;
D O I
10.1093/pnasnexus/pgad257
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The microscopic origins of terahertz (THz) vibrational modes in biological systems are an active and open area of current research. Recent experiments [Phys Rev X. 8, 031061 (2018)] have revealed the presence of a pronounced mode at & SIM;0.3 THz in fluorophore-decorated bovine serum albumin (BSA) protein in aqueous solution under nonequilibrium conditions induced by optical pumping. This result was heuristically interpreted as a collective elastic fluctuation originating from the activation of a low-frequency phonon mode. In this work, we show that the sub-THz spectroscopic response emerges in a statistically significant manner (>2s) from such collective behavior, illustrating how photoexcitation can alter specific THz vibrational modes. We revisit the theoretical analysis with proof-of-concept molecular dynamics that introduce optical excitations into the simulations. Using information theory techniques, we show that these excitations can give rise to a multiscale response involving two optically excited chromophores (tryptophans), other amino acids in the protein, ions, and water. Our results motivate new experiments and fully nonequilibrium simulations to probe these phenomena, as well as the refinement of atomistic models of Frohlich condensates that are fundamentally determined by nonlinear interactions in biology.
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页数:13
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共 65 条
[1]   Gromacs: High performance molecular simulations through multi-level parallelism from laptops to supercomputers [J].
Abraham, Mark James ;
Murtola, Teemu ;
Schulz, Roland ;
Páll, Szilárd ;
Smith, Jeremy C. ;
Hess, Berk ;
Lindah, Erik .
SoftwareX, 2015, 1-2 :19-25
[2]   LOW-FREQUENCY ELASTIC RESPONSE OF A SPHERICAL-PARTICLE [J].
BASTRUKOV, SI .
PHYSICAL REVIEW E, 1994, 49 (04) :3166-3170
[3]   Water Determines the Structure and Dynamics of Proteins [J].
Bellissent-Funel, Marie-Claire ;
Hassanali, Ali ;
Havenith, Martina ;
Henchman, Richard ;
Pohl, Peter ;
Sterpone, Fabio ;
van der Spoel, David ;
Xu, Yao ;
Garcia, Angel E. .
CHEMICAL REVIEWS, 2016, 116 (13) :7673-7697
[4]   An exact solution for the modified nonlinear Schrodinger's equation for Davydov solitons in α-helix proteins [J].
Biswas, Anjan ;
Moran, Allison ;
Milovic, Daniela ;
Majid, Fayequa ;
Biswas, Keka C. .
MATHEMATICAL BIOSCIENCES, 2010, 227 (01) :68-71
[5]   The terahertz dance of water with the proteins: the effect of protein flexibility on the dynamical hydration shell of ubiquitin [J].
Born, Benjamin ;
Kim, Seung Joong ;
Ebbinghaus, Sinion ;
Gruebele, Martin ;
Havenith, Martina .
FARADAY DISCUSSIONS, 2009, 141 :161-173
[7]   Relaxation Dynamics of Tryptophan in Water: A UV Fluorescence Up-Conversion and Molecular Dynamics Study [J].
Braem, O. ;
Ajdarzadeh Oskouei, A. ;
Tortschanoff, A. ;
van Mourik, F. ;
Madrid, M. ;
Echave, J. ;
Cannizzo, A. ;
Chergui, M. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2010, 114 (34) :9034-9042
[8]   Analysis of the Hydration Water around Bovine Serum Albumin Using Terahertz Coherent Synchrotron Radiation [J].
Bye, Jordan W. ;
Meliga, Stefano ;
Ferachou, Denis ;
Cinque, Gianfelice ;
Zeitler, J. Axel ;
Falconer, Robert J. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2014, 118 (01) :83-88
[9]   A computational investigation of thermodynamics, structure, dynamics and solvation behavior in modified water models [J].
Chatterjee, Swaroop ;
Debenedetti, Pablo G. ;
Stillinger, Frank H. ;
Lynden-Bell, Ruth M. .
JOURNAL OF CHEMICAL PHYSICS, 2008, 128 (12)
[10]   Low-Frequency Protein Motions Coupled to Catalytic Sites [J].
Cheatum, Christopher M. .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, VOL 71, 2020, 71 :267-288