RESUMEN
Endonucleolytic removal of 5'-leader sequences from tRNA precursor transcripts (pre-tRNAs) by ribonuclease P (RNase P) is essential for protein synthesis. Beyond RNA-based RNase P enzymes, protein-only versions of the enzyme exert this function in various eukarya (there termed PRORPs) and in some bacteria (Aquifex aeolicus and close relatives); both enzyme types belong to distinct subgroups of the PIN domain metallonuclease superfamily. Homologs of Aquifex RNase P (HARPs) are also expressed in some other bacteria and many archaea, where they coexist with RNA-based RNase P and do not represent the main RNase P activity. Here, we solved the structure of the bacterial HARP from Halorhodospira halophila by cryo-electron microscopy, revealing a novel screw-like dodecameric assembly. Biochemical experiments demonstrate that oligomerization is required for RNase P activity of HARPs. We propose that the tRNA substrate binds to an extended spike-helix (SH) domain that protrudes from the screw-like assembly to position the 5'-end in close proximity to the active site of the neighboring dimer. The structure suggests that eukaryotic PRORPs and prokaryotic HARPs recognize the same structural elements of pre-tRNAs (tRNA elbow region and cleavage site). Our analysis thus delivers the structural and mechanistic basis for pre-tRNA processing by the prokaryotic HARP system.
Asunto(s)
Halorhodospira halophila/genética , Ribonucleasa P/genética , Archaea/genética , Archaea/metabolismo , Bacterias/genética , Bacterias/metabolismo , Microscopía por Crioelectrón , Halorhodospira halophila/metabolismo , Ribonucleasa P/metabolismoRESUMEN
The role of the significant flexibility of the ß-turn in photoactive yellow protein (PYP) due to Gly115 was studied. G115A and G115P mutations were observed to accelerate the photocycle and shift the equilibrium between the late photocycle intermediate (pB) and its precursor (pR) toward pR. Thermodynamic analysis of dark-state recovery from pB demonstrated that the transition state (pB⧧) has a negative change in transition heat capacity, suggesting that an exposed hydrophobic surface of pB is buried in pB⧧. Fourier transform infrared spectroscopy showed that the structural ensemble of pB is populated by the compact structure in G115P. Taken together, the rigid structure induced by mutation of Gly115 facilitates its transition to pB⧧, which adopts a substantially more compact structure as opposed to the ensemble-averaged structure of pB. The photocycle kinetics of PYP may be fine-tuned by modulating the flexibility of the 115 loop to activate an appropriate number of transducer proteins.
Asunto(s)
Proteínas Bacterianas/metabolismo , Halorhodospira halophila/química , Fotorreceptores Microbianos/metabolismo , Termodinámica , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Halorhodospira halophila/metabolismo , Cinética , Modelos Moleculares , Mutación , Procesos Fotoquímicos , Fotorreceptores Microbianos/química , Fotorreceptores Microbianos/genéticaRESUMEN
Halophiles utilize two distinct osmoprotection strategies. The accumulation of organic compatible solutes such as glycine betaine does not perturb the functioning of cytoplasmic components, but represents a large investment of energy and carbon. KCl is an energetically attractive alternative osmoprotectant, but requires genome-wide modifications to establish a highly acidic proteome. Most extreme halophiles are optimized for the use of one of these two strategies. Here we examine the extremely halophilic Proteobacterium Halorhodospira halophila and report that medium K+ concentration dramatically alters its osmoprotectant use. When grown in hypersaline media containing substantial K+ concentrations, H. halophila accumulates molar concentrations of KCl. However, at limiting K+ concentrations the organism switches to glycine betaine as its major osmoprotectant. In contrast, the closely related organism Halorhodospira halochloris is limited to using compatible solutes. H. halophila performs both de novo synthesis and uptake of glycine betaine, matching the biosynthesis and transport systems encoded in its genome. The medium K+ concentration (~10 mM) at which the KCl to glycine betaine osmoprotectant switch in H. halophila occurs is near the K+ content of the lake from which it was isolated, supporting an ecological relevance of this osmoprotectant strategy.
Asunto(s)
Betaína/metabolismo , Halorhodospira halophila/metabolismo , Cloruro de Potasio/metabolismo , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Betaína/análisis , Halorhodospira halophila/genética , Halorhodospira halophila/crecimiento & desarrollo , Concentración Osmolar , Cloruro de Potasio/análisis , Proteoma , EspectrofotometríaRESUMEN
A novel optical holographic technique is presented to simultaneously measure both the real and imaginary components of the complex refractive index (CRI) of a protein solution over a wide visible wavelength range. Quantitative phase imaging was employed to precisely measure the optical field transmitted from a protein solution, from which the CRIs of the protein solution were retrieved using the Fourier light scattering technique. Using this method, we characterized the CRIs of the two dominant structural states of a photoactive yellow protein solution over a broad wavelength range (461-582 nm). The significant CRI deviation between the two structural states was quantified and analysed. The results of both states show the similar overall shape of the expected rRI obtained from the Kramers-Kronig relations.
Asunto(s)
Proteínas Bacterianas/química , Halorhodospira halophila/metabolismo , Fotorreceptores Microbianos/química , Refractometría/métodos , Dispersión Dinámica de Luz/métodos , Análisis de Fourier , Microscopía de Contraste de Fase/métodosRESUMEN
Using various spectroscopic techniques such as UV-visible spectroscopy, circular dichroism spectroscopy, NMR spectroscopy, small-angle X-ray scattering, transient grating, and transient absorption techniques, we investigated how cell-mimetic environments made by crowding influence the photocycle of photoactive yellow protein (PYP) in terms of the molecular volume change and kinetics. Upon addition of molecular crowding agents, the ratio of the diffusion coefficient of the blue-shifted intermediate (pB) to that of the ground species (pG) significantly changes from 0.92 and approaches 1.0. This result indicates that the molecular volume change accompanied by the photocycle of PYP in molecularly crowded environments is much smaller than that which occurs in vitro and that the pB intermediate under crowded environments favors a compact conformation due to the excluded volume effect. The kinetics of the photocycle of PYP in cell-mimetic environments is greatly decelerated by the dehydration, owing to the interaction between the protein and small crowding agents, but is barely affected by the excluded volume effect. The results lead to the inference that the signaling transducer of PYP may not necessarily utilize the conformational change of PYP to sense the signaling state.
Asunto(s)
Proteínas Bacterianas/química , Proteínas Bacterianas/metabolismo , Halorhodospira halophila/metabolismo , Fotorreceptores Microbianos/química , Fotorreceptores Microbianos/metabolismo , Biomimética , Halorhodospira halophila/química , Cinética , Procesos FotoquímicosRESUMEN
A theoretical study on the NMR shifts of the hydrogen bond network around the chromophore, para-coumaric acid (pCA), of photoactive yellow protein (PYP) is presented. Previous discrepancies between theoretical and experimental studies are resolved by our findings of a previously unknown rapid conformational exchange near the active site of PYP. This exchange caused by the rotation of Thr50 takes place in the ground state of PYP's active site and results in three effectively energetically equal conformations characterized by the formation of new hydrogen bonds, all of which contribute to the overall NMR signals of the investigated protons. In light of these findings, we are able to successfully explain the experimental results and provide valuable insight into the behavior of PYP in solution. We further investigated related PYP mutants (T50V, E46Q, and Y42F), and found the same conformational exchange in E46Q and Y42F to be responsible for the experimentally observed NMR and UV/vis spectra.
Asunto(s)
Proteínas Bacterianas/química , Fotorreceptores Microbianos/química , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Dominio Catalítico , Halorhodospira halophila/metabolismo , Enlace de Hidrógeno , Modelos Moleculares , Mutagénesis Sitio-Dirigida , Resonancia Magnética Nuclear Biomolecular , Fotorreceptores Microbianos/genética , Fotorreceptores Microbianos/metabolismo , Estructura Terciaria de Proteína , Teoría Cuántica , TermodinámicaRESUMEN
UV excitation and IR absorption spectroscopy on jet-cooled molecules is used to study the conformational heterogeneity of methyl 4-hydroxycinnamate, a model chromophore of the Photoactive Yellow Protein (PYP), and to determine the spectroscopic properties of the various conformers. UV-UV depletion spectroscopy identifies four different species with distinct electronic excitation spectra. Quantum chemical calculations argue that these species are associated with different conformers involving the s-cis/s-trans configuration of the ester with respect to the propenyl C-C single bond and the syn/anti orientation of the phenolic OH group. IR-UV hole-burning spectroscopy is used to record their IR absorption spectra in the fingerprint region. Comparison with IR absorption spectra predicted by quantum chemical calculations provides vibrational markers for each of the conformers, on the basis of which each of the species observed with UV-UV depletion spectroscopy is assigned. Although both DFT and wave function methods reproduce experimental frequencies, we find that calculations at the MP2 level are necessary to obtain agreement with experimentally observed intensities. To elucidate the role of the environment, we compare the IR spectra of the isolated conformers with IR spectra of methyl 4-hydroxycinnamate-water clusters, and with IR spectra of methyl 4-hydroxycinnamate in solution.
Asunto(s)
Cinamatos/química , Gases/química , Proteínas Bacterianas/química , Proteínas Bacterianas/metabolismo , Halorhodospira halophila/metabolismo , Isomerismo , Conformación Molecular , Fotorreceptores Microbianos/química , Fotorreceptores Microbianos/metabolismo , Teoría Cuántica , Espectrofotometría Infrarroja , Espectrofotometría Ultravioleta , Agua/químicaRESUMEN
The chromophore of the photoactive yellow protein (PYP), the photoreceptor in the photomotility of the bacterium Halorhodospira halophila, is a deprotonated para-coumaric thioester linked to the side residue of a cysteine residue. The photophysics of the PYP chromophore is conveniently modeled with para-hydroxycinnamic thiophenyl esters. Herein, we report the first direct evidence, obtained with X-ray diffraction, of photodimerization of a para-hydroxycinnamic thiophenyl ester in single crystalline state. This result represents the first direct observation of [2+2] dimerization of a model PYP chromophore, and demonstrates that even very weak light in the visible region is capable of inducing parallel radical reactions in PYP from the excited state of the chromophore, in addition to the main reaction pathway (trans-cis isomerization). This PYP model system adds an interesting example to the known solid-state photodimerizations, because unlike the anhydrous crystal (which is not capable of sustaining the stress and disintegrates in the course of photodimerization), a single water molecule "dilutes" the structure to the extent sufficient for single-crystal-to-single-crystal reaction.
Asunto(s)
Proteínas Bacterianas/química , Halorhodospira halophila/química , Procesos Fotoquímicos , Fotorreceptores Microbianos/química , Multimerización de Proteína , Proteínas Bacterianas/metabolismo , Cristalografía por Rayos X , Ésteres/química , Halorhodospira halophila/metabolismo , Luz , Modelos Moleculares , Fotorreceptores Microbianos/metabolismo , Estructura Cuaternaria de ProteínaRESUMEN
Photoinduced ionization of the chromophore inside photoactive yellow protein (PYP) was investigated by ultrafast spectroscopy in the visible and near-infrared spectral regions. An absorption band that extended from around 550 to 850 nm was observed and ascribed to solvated electrons, ejected from the p-hydroxycinnamic acid anion chromophore upon the absorption of two 400 nm photons. Global kinetic analysis showed that the solvated electron absorption decayed in two stages: a shorter phase of around 10 ps and a longer phase of more than 3 ns. From a simulation based on a diffusion model we conclude that the diffusion rate of the electron is about 0.8 Å(2)/ps in wild type PYP, and that the electron is ejected to a short distance of only several angstroms away from the chromophore. The chromophore-protein pocket appears to provide a water-similar local environment for the electron. Because mutations at different places around the chromophore have different effect on the electron recombination dynamics, we suggest that solvated electrons could provide a new method to investigate the local dielectric environment inside PYP and thus help to understand the role of the protein in the photoisomerization process.
Asunto(s)
Proteínas Bacterianas/química , Fotorreceptores Microbianos/química , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Difusión , Electrones , Halorhodospira halophila/metabolismo , Cinética , Mutación , Fotorreceptores Microbianos/genética , Fotorreceptores Microbianos/metabolismo , Espectrofotometría , Espectrofotometría InfrarrojaRESUMEN
Impulsive excitation of molecular vibration is known to induce wave packets in both the ground state and excited state. Here, the ultrafast dynamics of PYP was studied by pump-probe spectroscopy using a sub-8 fs pulse laser at 400 nm. The broadband spectrum of the UV pulse allowed us to detect the pump-probe signal covering 360-440 nm. The dependence of the vibrational phase of the vibrational mode around 1155 cm(-1) on the probe photon energy was observed for the first time to our knowledge. The vibrational mode coupled to the electronic transition observed in the probe spectral ranges of 2.95-3.05 and 3.15-3.35 eV was attributed to the wave packets in the ground state and the excited state, respectively. The frequencies in the ground state and excited state were determined to be 1155 ± 1 and 1149 ± 1 cm(-1), respectively. The frequency difference is due to change after photoexcitation. This means a reduction of the bond strength associated with π-π* excitation, which is related to the molecular structure change associated with the primary isomerization process in the photocycle in PYP. Real-time vibrational modes at low frequency around 138, 179, 203, 260, and 317 cm(-1) were also observed and compared with the Raman spectrum for the assignment of the vibrational wave packet.
Asunto(s)
Proteínas Bacterianas/química , Rayos Láser , Fotorreceptores Microbianos/química , Proteínas Bacterianas/metabolismo , Ácidos Cumáricos/química , Electrones , Análisis de Fourier , Halorhodospira halophila/metabolismo , Fotorreceptores Microbianos/metabolismo , Espectrofotometría Ultravioleta , Espectrometría Raman , Factores de Tiempo , VibraciónRESUMEN
The tricarboxylic acid citric acid is a key intermediary metabolite in organisms from all domains of the tree of life. Surprisingly, this metabolite specifically interacts with the light-induced signaling state of the photoactive yellow protein (PYP), such that, at 30 mM, it retards recovery of this state to the stable ground state of the protein with up to 30%, in the range from pH 4.5 to pH 7. We have performed a detailed UV/vis spectroscopic study of the recovery of the signaling state of wild type (WT) PYP and two mutants, H108F and Δ25-PYP, derived from this protein, as a function of pH and the concentration of citric acid. This revealed that it is the dianionic form of citric acid that binds to the pB state of PYP. Its binding site is located in between the N-terminal cap and central ß-sheet of PYP, which is accessible only in the signaling state of the protein. The obtained results show how changes in the distribution of subspecies of the signaling state of PYP influence the rate of ground state recovery.
Asunto(s)
Proteínas Bacterianas/metabolismo , Ácido Cítrico/metabolismo , Hidrógeno/metabolismo , Fotorreceptores Microbianos/metabolismo , Sustitución de Aminoácidos , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Sitios de Unión , Ácido Cítrico/química , Halorhodospira halophila/metabolismo , Hidrógeno/química , Concentración de Iones de Hidrógeno , Cinética , Simulación del Acoplamiento Molecular , Fotorreceptores Microbianos/química , Fotorreceptores Microbianos/genética , Estabilidad Proteica , Estructura Terciaria de Proteína , Espectrofotometría UltravioletaRESUMEN
For several years following the discovery and characterization of the first PYP, from Halorhodospira halophila, it was thought that this photoactive protein was quite unique, notwithstanding the isolation of two additional examples in rapid succession. Mainly because of genomic and metagenomic analyses, we have now learned that more than 140 PYP genes occur in a wide variety of bacteria and metabolic niches although the protein has not been isolated in most cases. The amino acid sequences and physical properties permit their organization into at least seven groups that are also likely to be functionally distinct. Based upon action spectra and the wavelength of maximum absorbance, it was speculated nearly 20 years ago but never proven that Hr. halophila PYP was involved in phototaxis. Nevertheless, in only one instance has the functional role and interaction partner for a PYP been experimentally proven, in Rs. centenum Ppr. Genetic context is one of several types of evidence indicating that PYP is potentially involved in a number of diverse functional roles. The interaction with other sensors to modulate their activity stands out as the single most prominent role for PYP. In this review, we have attempted to summarize the evidence for the functional roles and interaction partners for some 26 of the 35 named species of PYP, which should be considered the basis for further focused molecular and biochemical research.
Asunto(s)
Proteínas Bacterianas/genética , Halorhodospira halophila/genética , Fotorreceptores Microbianos/fisiología , Rhodobacter/genética , Secuencia de Aminoácidos , Proteínas Bacterianas/química , Proteínas Bacterianas/clasificación , Proteínas Bacterianas/metabolismo , Halorhodospira halophila/metabolismo , Datos de Secuencia Molecular , Fotorreceptores Microbianos/química , Fotorreceptores Microbianos/clasificación , Fotorreceptores Microbianos/genética , Fotorreceptores Microbianos/metabolismo , Filogenia , Mapeo de Interacción de Proteínas , Rhodobacter/metabolismo , Alineación de SecuenciaRESUMEN
We report on a detailed theoretical analysis, based on extensive ab initio calculations at the CC2 level, of the S(1) potential energy surface (PES) of the photoactive yellow protein (PYP) chromophore. The chromophore's photoisomerization pathway is shown to be fairly complex, involving an intimate coupling between single-bond and double-bond torsions. Furthermore, these torsional modes are shown to couple to a third coordinate of hydrogen out-of-plane (HOOP) type whose role in the isomerization is here identified for the first time. In addition, it is demonstrated that hydrogen bonding at the phenolate moiety of the chromophore can hinder the single-bond torsion and thus facilitates double-bond isomerization. These results suggest that the interplay between intramolecular factors and H-bonding determines the isomerization in native PYP.
Asunto(s)
Proteínas Bacterianas/química , Halorhodospira halophila/química , Fotorreceptores Microbianos/química , Proteínas Bacterianas/metabolismo , Halorhodospira halophila/metabolismo , Enlace de Hidrógeno , Luz , Modelos Moleculares , Procesos Fotoquímicos/efectos de la radiación , Fotorreceptores Microbianos/metabolismo , Estereoisomerismo , Termodinámica , Torsión MecánicaRESUMEN
Photocontrolled transcription factors could be powerful tools for probing the roles of transcriptional processes in a variety of settings. Previously, we designed a photocontrolled DNA-binding protein based on a fusion between the bZIP region of GCN4 and photoactive yellow protein from Halorhodospira halophila [Morgan, S. A., et al. (2010) J. Mol. Biol. 399, 94-112]. Here we report a structure-based attempt to improve the degree of photoswitching observed with this chimeric protein. Using computational design tools PoPMuSiC 2.0, Rosetta, Eris, and bCIPA, we identified a series of single- and multiple-point mutations that were expected to stabilize the folded dark state of the protein and thereby enhance the degree of photoswitching. While a number of these mutations, particularly those that introduced a hydrophobic residue at position 143, did significantly enhance dark-state protein stability as judged by urea denaturation studies, dark-state stability did not correlate directly with the degree of photoswitching. Instead, the influence of mutations on the degree of photoswitching was found to be related to their effects on the degree to which DNA binding slowed the pB to pG transition in the PYP photocycle. One mutant, K143F, caused an â¼10-fold slowing of the photocycle and also showed the largest difference in the apparent K(d) for DNA binding, 3.5-fold lower, upon irradiation. This change in the apparent K(d) causes a 12-fold enhancement in the fraction bound DNA upon irradiation due to the cooperativity of DNA binding by this family of proteins. The results highlight the strengths and weaknesses of current approaches to a practical problem in protein design and suggest strategies for further improvement of designed photocontrolled transcription factors.
Asunto(s)
Proteínas de Unión al ADN/síntesis química , Luz , Proteínas Luminiscentes/síntesis química , Ingeniería de Proteínas/métodos , Secuencia de Aminoácidos , Cristalografía por Rayos X , ADN/metabolismo , Proteínas de Unión al ADN/genética , Halorhodospira halophila/genética , Halorhodospira halophila/metabolismo , Proteínas Luminiscentes/genética , Modelos Moleculares , Datos de Secuencia Molecular , Mutagénesis Sitio-Dirigida/métodos , Procesos Fotoquímicos , Estructura Cuaternaria de Proteína , Estructura Secundaria de Proteína/genética , Proteínas Recombinantes/síntesis química , Proteínas Recombinantes/genéticaRESUMEN
UV light below 300 nm is shown to generate the first photocycle intermediate in the blue light photoreceptor Photoactive Yellow Protein. Fluorescence and ultrafast transient absorption measurements indicate two excitation pathways: UV-B absorption by the chromophore and Fluorescence Resonant Energy Transfer (FRET) from tryptophan and tyrosine residues.
Asunto(s)
Proteínas Bacterianas/química , Fotorreceptores Microbianos/química , Rayos Ultravioleta , Transferencia Resonante de Energía de Fluorescencia , Halorhodospira halophila/metabolismo , Halorhodospira halophila/efectos de la radiación , Cinética , Teoría Cuántica , Triptófano/química , Tirosina/químicaRESUMEN
Blue-light photoreceptors play a pivotal role in detecting the quality and quantity of light in the environment, controlling a wide range of biological responses. Several families of blue-light photoreceptors have been characterized in detail using biophysics and biochemistry, beginning with photon absorption, through intervening signal transduction, to regulation of biological activities. Here we review the light oxygen voltage, cryptochrome, and sensors of blue light using FAD families, three different groups of proteins that offer distinctly different modes of photochemical activation and signal transduction yet play similar roles in a vast array of biological responses. We cover mechanisms of light activation and propagation of conformational responses that modulate protein-protein interactions involved in biological signaling. Discovery and characterization of these processes in natural proteins are now allowing the design of photoregulatable engineered proteins, facilitating the generation of novel reagents for biochemical and cell biological research.
Asunto(s)
Proteínas Bacterianas/metabolismo , Criptocromos/metabolismo , Flavoproteínas/metabolismo , Células Fotorreceptoras/metabolismo , Fotorreceptores Microbianos/metabolismo , Animales , Bacterias/química , Bacterias/metabolismo , Proteínas Bacterianas/química , Biotecnología , Criptocromos/química , Flavoproteínas/química , Halorhodospira halophila/química , Halorhodospira halophila/metabolismo , Humanos , Luz , Modelos Moleculares , Procesos Fotoquímicos , Células Fotorreceptoras/química , Fotorreceptores Microbianos/química , Mapas de Interacción de Proteínas , Estructura Terciaria de Proteína , Transducción de SeñalAsunto(s)
Proteínas Bacterianas/química , Cisteína/química , Fosfinas/química , Fotorreceptores Microbianos/química , Sustitución de Aminoácidos , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Catálisis , Halorhodospira halophila/metabolismo , Paladio/química , Fotorreceptores Microbianos/genética , Fotorreceptores Microbianos/metabolismo , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismoRESUMEN
Photocontrolled transcription factors could be powerful tools for probing the role of transcriptional processes in settings that are spatially or temporally complex. We report the structure-based design of a photocontrolled bZIP-type DNA binding protein that is a hybrid of the prototypical homodimeric bZIP protein GCN4 and photoactive yellow protein (PYP), a blue-light-sensitive protein from Halorhodospira halophila. A fusion of the C-terminal zipper region of GCN4-bZIP with the N-terminal cap of PYP was designed based on examination of available crystal structure data, analysis of amino acid preference rules for leucine zippers, and mutational and amino acid conservation data for PYP, together with Rosetta-guided structural modeling. The designed fusion protein GCN4Delta25PYP-v2 is monomeric in the dark; fluorescence, circular dichroism, NMR, and analytical ultracentrifugation data indicate that the zipper domain is hidden. DNA binding in the dark causes substantial structural reorganization of GCN4Delta25PYP-v2 with concomitant slowing of the photocycle, consistent with conformational coupling of the DNA binding domain and the light-sensitive domain of the protein. Consistent with this finding, blue-light irradiation causes a 2-fold increase in specific DNA binding affinity that reverses in the dark. The structure-based approach suggests strategies for enhancing this activity and for producing a family of related photocontrolled proteins for manipulating bZIP activity.
Asunto(s)
Proteínas Bacterianas/química , Proteínas de Unión al ADN/química , Secuencia de Aminoácidos , Proteínas Bacterianas/metabolismo , Proteínas de Unión al ADN/metabolismo , Dimerización , Halorhodospira halophila/metabolismo , Modelos Moleculares , Datos de Secuencia Molecular , Conformación Proteica , Rayos UltravioletaAsunto(s)
Proteínas Bacterianas/química , Luz , Fotorreceptores Microbianos/química , Conformación Proteica/efectos de la radiación , Halorhodospira halophila/metabolismo , Modelos Moleculares , Simulación de Dinámica Molecular , Pliegue de Proteína/efectos de la radiación , Estructura Secundaria de Proteína/efectos de la radiación , Estructura Terciaria de Proteína/efectos de la radiación , Termodinámica , Factores de TiempoRESUMEN
Understanding the dynamics of large-scale conformational changes in proteins still poses a challenge for molecular simulations. We employ transition path sampling of explicit solvent molecular dynamics trajectories to obtain atomistic insight in the reaction network of the millisecond timescale partial unfolding transition in the photocycle of the bacterial sensor photoactive yellow protein. Likelihood maximization analysis predicts the best model for the reaction coordinates of each substep as well as tentative transition states, without further simulation. We find that the unfolding of the alpha-helical region 43-51 is followed by sequential solvent exposure of both Glu46 and the chromophore. Which of these two residues is exposed first is correlated with the presence of a salt bridge that is part of the N-terminal domain. Additional molecular dynamics simulations indicate that the exposure of the chromophore does not result in a productive pathway. We discuss several possibilities for experimental validation of these predictions. Our results open the way for studying millisecond conformational changes in other medium-sized (signaling) proteins.