Literature DB >> 8744330

Near-infrared spectra of Scapharca homodimeric hemoglobin: characterization of the deoxy and photodissociated derivatives.

J Huang1, M Leone, A Boffi, J M Friedman, E Chiancone.   

Abstract

The near-infrared charge transfer band at 760 nm (band III) has been investigated in deoxy and photodissociated dimeric Scapharca hemoglobin. At 300 K, the 10-ns spectrum of the carbonmonoxy derivative photoproduct is shifted by about 6 nm toward longer wavelengths with respect to the deoxy spectrum, both in buffer and in glycerol/buffer solutions. Moreover, the band III peak occurs at about the same wavelength at 300 K and at 10 K for the 10-ns photodissociated derivative, whereas in the deoxy derivative large changes in peak position and linewidth are observed as a function of temperature. These findings suggest that in dimeric Scapharca hemoglobin the photoproduct has not relaxed after 10 ns. The complete time dependence of the relaxation process has been studied both in buffer and in glycerol/buffer solutions at room temperature. The relaxation from the photoproduct to the deoxy species occurs on a microsecond time scale, in line with recent optical absorption and resonance Raman measurements.

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Year:  1996        PMID: 8744330      PMCID: PMC1225272          DOI: 10.1016/S0006-3495(96)79862-4

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  25 in total

1.  Spectral broadening in biomolecules.

Authors: 
Journal:  Phys Rev Lett       Date:  1986-09-08       Impact factor: 9.161

2.  Protein conformational relaxation following photodissociation of CO from carbonmonoxymyoglobin: picosecond circular dichroism and absorption studies.

Authors:  X L Xie; J D Simon
Journal:  Biochemistry       Date:  1991-04-16       Impact factor: 3.162

3.  Structural and functional significance of inhomogeneous line broadening of band III in hemoglobin and Fe-Mn hybrid hemoglobins.

Authors:  M D Chavez; S H Courtney; M R Chance; D Kiula; J Nocek; B M Hoffman; J M Friedman; M R Ondrias
Journal:  Biochemistry       Date:  1990-05-22       Impact factor: 3.162

4.  Time-resolved Raman spectroscopy with subpicosecond resolution: vibrational cooling and delocalization of strain energy in photodissociated (carbonmonoxy)hemoglobin.

Authors:  J W Petrich; J L Martin; D Houde; C Poyart; A Orszag
Journal:  Biochemistry       Date:  1987-12-01       Impact factor: 3.162

Review 5.  Low temperature optical absorption spectroscopy: an approach to the study of stereodynamic properties of hemeproteins.

Authors:  A Cupane; M Leone; E Vitrano; L Cordone
Journal:  Eur Biophys J       Date:  1995       Impact factor: 1.733

6.  Conformational relaxation and ligand binding in myoglobin.

Authors:  A Ansari; C M Jones; E R Henry; J Hofrichter; W A Eaton
Journal:  Biochemistry       Date:  1994-05-03       Impact factor: 3.162

7.  Dimeric and tetrameric hemoglobins from the mollusc Scapharca inaequivalvis. Structural and functional properties.

Authors:  E Chiancone; P Vecchini; D Verzili; F Ascoli; E Antonini
Journal:  J Mol Biol       Date:  1981-11-05       Impact factor: 5.469

8.  Structural heterogeneity of the Fe(2+)-N epsilon (HisF8) bond in various hemoglobin and myoglobin derivatives probed by the Raman-active iron histidine stretching mode.

Authors:  H Gilch; R Schweitzer-Stenner; W Dreybrodt
Journal:  Biophys J       Date:  1993-10       Impact factor: 4.033

9.  Heme-heme interactions in a homodimeric cooperative hemoglobin. Evidence from transient Raman scattering.

Authors:  D L Rousseau; S Song; J M Friedman; A Boffi; E Chiancone
Journal:  J Biol Chem       Date:  1993-03-15       Impact factor: 5.157

10.  Stereodynamic properties of the cooperative homodimeric Scapharca inaequivalvis hemoglobin studied through optical absorption spectroscopy and ligand rebinding kinetics.

Authors:  A Boffi; D Verzili; E Chiancone; M Leone; A Cupane; V Militello; E Vitrano; L Cordone; W Yu; E E Di Iorio
Journal:  Biophys J       Date:  1994-10       Impact factor: 4.033

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  2 in total

1.  Structural and dynamic properties of the homodimeric hemoglobin from Scapharca inaequivalvis Thr-72-->Ile mutant: molecular dynamics simulation, low temperature visible absorption spectroscopy, and resonance Raman spectroscopy studies.

Authors:  M Falconi; A Desideri; A Cupane; M Leone; G Ciccotti; E S Peterson; J M Friedman; A Gambacurta; F Ascoli
Journal:  Biophys J       Date:  1998-11       Impact factor: 4.033

2.  Ultrafast coherent motion and helix rearrangement of homodimeric hemoglobin visualized with femtosecond X-ray solution scattering.

Authors:  Yunbeom Lee; Jong Goo Kim; Sang Jin Lee; Srinivasan Muniyappan; Tae Wu Kim; Hosung Ki; Hanui Kim; Junbeom Jo; So Ri Yun; Hyosub Lee; Kyung Won Lee; Seong Ok Kim; Marco Cammarata; Hyotcherl Ihee
Journal:  Nat Commun       Date:  2021-06-16       Impact factor: 14.919

  2 in total

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