Literature DB >> 202327

The effect of quaternary structure on the state of the alpha and beta subunits within nitrosyl haemoglobin. Low temperature photodissociation and the ESR spectra.

K Nagai, H Hori, S Yoshida, H Sakamoto, H Morimoto.   

Abstract

Photodissociation of nitrosyl haemoglobin and nitrosyl hybrids, in which either the alpha or beta subunit is in the nitrosyl form has been stidued at liquid helium temperature (4.2 degrees K) by electron spin resonance and optical absorption spectroscopy. In the presence of inositol hexaphosphate, the photodissociated form of nitrosyl haemoglobin showed an anomalous absorption spectrum in the near infrared region. The experiments with nitrosyl hybrids showed that the alphaNO subunit within the T state haemoglobin is predominantly responsible for the anomalous photodissociated form and the ESR spectrum with three distinct hypefines. The ESR spectrum of alphaNO2betadeoxy2 with inositol hexaphosphate appeared to be very similar to that of the 5-coordinated NO-haem complexes but the absorption spectrum of its photodissociated form was similar to none of protoporphyrin Fe(II) derivatives so far reported. This result suggests that the anomalous photodissociated form may be attributable to some structural distortion of porphyrin or a new electronic state of the haem with different spin state from that of deoxyhaemoglobin.

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Year:  1978        PMID: 202327     DOI: 10.1016/0005-2795(78)90443-9

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

1.  Ascorbic acid induces nitric oxide production in human leukocytes.

Authors:  Z V Kuropteva; T T Zhumabaeva; L M Baider; A V Aleshchenko
Journal:  Dokl Biochem Biophys       Date:  2001 Jan-Feb       Impact factor: 0.788

2.  The case of the missing NO-hemoglobin: spectral changes suggestive of heme redox reactions reflect changes in NO-heme geometry.

Authors:  Angela Fago; Alvin L Crumbliss; Jim Peterson; Linda L Pearce; Celia Bonaventura
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-26       Impact factor: 11.205

3.  Nitrosyl hemoglobin: EPR components at low temperatures.

Authors:  E Wajnberg; M P Linhares; L J el-Jaick; G Bemski
Journal:  Eur Biophys J       Date:  1992       Impact factor: 1.733

Review 4.  Contribution of Electron Paramagnetic Resonance to the studies of hemoglobin: the nitrosylhemoglobin system.

Authors:  G Bemski
Journal:  Mol Biol Rep       Date:  1997-11       Impact factor: 2.316

5.  Electron paramagnetic resonance- (EPR-) resolved kinetics of cryogenic nitric oxide recombination to cytochrome c oxidase and myoglobin.

Authors:  R LoBrutto; Y H Wei; S Yoshida; H L Van Camp; C P Scholes; T E King
Journal:  Biophys J       Date:  1984-02       Impact factor: 4.033

6.  Differences in Fe(II)-N epsilon(His-F8) stretching frequencies between deoxyhemoglobins in the two alternative quaternary structures.

Authors:  K Nagai; T Kitagawa
Journal:  Proc Natl Acad Sci U S A       Date:  1980-04       Impact factor: 11.205

7.  Origin of observed changes in 14N hyperfine interaction accompanying R leads to T transition in nitrosylhemoglobin.

Authors:  S K Mun; J C Chang; T P Das
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

8.  Haem conformation of amphibian nytrosylhaemoglobins detected by XANES spectroscopy.

Authors:  D Pozzi; G Amiconi; A Arcovito; M Girasole; A Congiu Castellano
Journal:  Eur Phys J E Soft Matter       Date:  2005-04       Impact factor: 1.890

9.  Cross-linking with O-raffinose lowers oxygen affinity and stabilizes haemoglobin in a non-cooperative T-state conformation.

Authors:  Yiping Jia; Somasundaram Ramasamy; Francine Wood; Abdu I Alayash; Joseph M Rifkind
Journal:  Biochem J       Date:  2004-12-01       Impact factor: 3.857

10.  Oxygen and CO binding to triply NO and asymmetric NO/CO hemoglobin hybrids.

Authors:  L Kiger; C Poyart; M C Marden
Journal:  Biophys J       Date:  1993-09       Impact factor: 4.033

  10 in total

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