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1.
Biochemistry ; 40(38): 11460-71, 2001 Sep 25.
Artículo en Inglés | MEDLINE | ID: mdl-11560494

RESUMEN

The P(r) to P(fr) transition of recombinant Synechocystis PCC 6803 phytochrome Cph1 and its N-terminal sensor domain Cph1Delta2 is accompanied by net acidification in unbuffered solution. The extent of this net photoreversible proton release was measured with a conventional pH electrode and increased from less than 0.1 proton released per P(fr) formed at pH 9 to between 0.6 (Cph1) and 1.1 (Cph1Delta2) H(+)/P(fr) at pH 6. The kinetics of the proton release were monitored at pH 7 and pH 8 using flash-induced transient absorption measurements with the pH indicator dye fluorescein. Proton release occurs with time constants of approximately 4 and approximately 20 ms that were also observed in parallel measurements of the photocycle (tau(3) and tau(4)). The number of transiently released protons per P(fr) formed is about one. This H(+) release phase is followed by a proton uptake phase of a smaller amplitude that has a time constant of approximately 270 ms (tau(5)) and is synchronous with the formation of P(fr). The acidification observed in the P(r) to P(fr) transition with pH electrodes is the net effect of these two sequential protonation changes. Flash-induced transient absorption measurements were carried out with Cph1 and Cph1Delta2 at pH 7 and pH 8. Global analysis indicated the presence of five kinetic components (tau(1)-tau(5): 5 and 300 micros and 3, 30, and 300 ms). Whereas the time constants were approximately pH independent, the corresponding amplitude spectra (B(1), B(3), and B(5)) showed significant pH dependence. Measurements of the P(r)/P(fr) photoequilibrium indicated that it is pH independent in the range of 6.5-9.0. Analysis of the pH dependence of the absorption spectra from 6.5 to 9.0 suggested that the phycocyanobilin chromophore deprotonates at alkaline pH in both P(r) and P(fr) with an approximate pK(a) of 9.5. The protonation state of the chromophore at neutral pH is therefore the same in both P(r) and P(fr). The light-induced deprotonation and reprotonation of Cph1 at neutral pH are thus due to pK(a) changes in the protein moiety, which are linked to conformational transitions occurring around 4 and 270 ms after photoexcitation. These transient structural changes may be relevant for signal transduction by this cyanobacterial phytochrome.


Asunto(s)
Proteínas Bacterianas , Cianobacterias/metabolismo , Concentración de Iones de Hidrógeno , Fitocromo/metabolismo , Fitocromo/efectos de la radiación , Proteínas Quinasas/metabolismo , Proteínas Quinasas/efectos de la radiación , Cinética , Luz , Mutagénesis , Fotoquímica , Fotorreceptores Microbianos , Fitocromo/química , Proteínas Quinasas/química , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Proteínas Recombinantes/efectos de la radiación , Eliminación de Secuencia , Soluciones , Espectrometría de Fluorescencia , Espectrofotometría
2.
Biochim Biophys Acta ; 1460(1): 60-74, 2000 Aug 30.
Artículo en Inglés | MEDLINE | ID: mdl-10984591

RESUMEN

Light-induced isomerization leads to orientational changes of the retinylidene chromophore of bacteriorhodopsin in its binding pocket. The chromophore reorientation has been characterized by the following methods: polarized absorption spectroscopy in the visible, UV and IR; polarized resonance Raman scattering; solid-state deuterium nuclear magnetic resonance; neutron and X-ray diffraction. Most of these experiments were performed at low temperatures with bacteriorhodopsin trapped in one or a mixture of intermediates. Time-resolved measurements at room temperature with bacteriorhodopsin in aqueous suspension can currently only be carried out with transient polarized absorption spectroscopy in the visible. The results obtained to date for the initial state and the K, L and M intermediates are presented and discussed. The most extensive data are available for the M intermediate, which plays an essential role in the function of bacteriorhodopsin. For this intermediate the various methods lead to a consistent picture: the curved all-trans polyene chain in the initial state straightens out in the M intermediate (13-cis) and the chain segment between C(5) and C(13) tilts upwards in the direction of the cytoplasmic surface. The kink at C(13) allows the positions of beta-ionone ring and Schiff base nitrogen to remain approximately fixed.


Asunto(s)
Bacteriorodopsinas/química , Membrana Púrpura/química , Análisis Espectral/métodos , Cristalografía/métodos , Espectroscopía de Resonancia Magnética/métodos , Fotoquímica , Retinaldehído/química , Espectrofotometría/métodos , Espectrometría Raman
3.
Neurol Neurochir Pol ; 31(6): 1245-51, 1997.
Artículo en Polaco | MEDLINE | ID: mdl-9678998

RESUMEN

The authors report a case of postradiotherapy cervical myelopathy after treatment of laryngeal cancer. The patient aged 61 was referred to a neurological hospital department with suspected metastasis of laryngeal cancer to the spine with symptoms indicating cervical cord lesion. During observation and after imaging examinations of the cervical spine cancer recurrence was excluded. History data and imaging methods served a basis for the diagnosis of postradiation myelopathy. The authors warn against too ready diagnosis of cancer in such cases and a repetition of radiotherapy.


Asunto(s)
Carcinoma de Células Escamosas/radioterapia , Vértebras Cervicales , Enfermedades Desmielinizantes/etiología , Neoplasias Laríngeas/radioterapia , Vaina de Mielina , Carcinoma de Células Escamosas/patología , Vértebras Cervicales/patología , Enfermedades Desmielinizantes/patología , Humanos , Neoplasias Laríngeas/patología , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Vaina de Mielina/patología , Radioterapia/efectos adversos
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