On the Configurational and Conformational Changes in Photoactive Yellow Protein that Leads to Signal Generation in Ectothiorhodospira halophila |
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Authors: | KJ Hellingwerf J Hendriks Th Gensch |
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Institution: | (1) Laboratory for Microbiology, Swammerdam Institute for Life sciences, BioCentrum Amsterdam, University of Amsterdam, The Netherlands;(2) Present address: Laboratory for Microbiology, Nieuwe Achtergracht 166, NL-1018 WV Amsterdam, The Netherlands |
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Abstract: | Photoactive Yellow Protein (PYP), a phototaxis photoreceptor from Ectothiorhodospira halophila, is a small water-soluble protein that iscrystallisable and excellently photo-stable. It can be activated with light( max= 446 nm), to enter a series of transientintermediates that jointly form the photocycle of this photosensor protein.The most stable of these transient states is the signalling state forphototaxis, pB.The spatial structure of the ground state of PYP, pG and the spectralproperties of the photocycle intermediates have been very well resolved.Owing to its excellent chemical- and photochemical stability, also the spatialstructure of its photocycle intermediates has been characterised with X-raydiffraction and multinuclear NMR spectroscopy. Surprisingly, the resultsobtained showed that their structure is dependent on the molecular contextin which they are formed. Therefore, a large range of diffraction-,scattering- and spectroscopic techniques is now being employed to resolvein detail the dynamical changes of the structure of PYP while it progressesthrough its photocycle. This approach has led to considerable progress,although some techniques still result in mutually inconsistent conclusionsregarding aspects of the structure of particular intermediates.Recently, significant progress has also been made with simulations withmolecular dynamics analyses of the initial events that occur in PYP uponphoto activation. The great challenge in this field is to eventually obtainagreement between predicted dynamical alterations in PYP structure, asobtained with the MD approach and the actually measured dynamicalchanges in its structure as evolving during photocycle progression. |
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Keywords: | 4-hydroxy-cinnamic acid contact dependence hysteresis photoactive yellow protein photo-isomerisation polarization spectroscopy protein dynamics time-resolved X-ray diffraction time-resolved FTIR spectroscopy transient intermediates |
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