Literature DB >> 3828461

Resonance Raman studies of dioxygen and carbon monoxide binding to imidazole-appended hemes.

N T Yu, H M Thompson, C K Chang.   

Abstract

Resonance Raman spectroscopy has been employed to probe the effects of proximal base strain on the bonding of O2 and CO in three synthetic hemins with covalently linked imidazole ligands. The strain is introduced by varying the length of the imidazole-containing side chain and by restricting the side chain flexibility with a phenyl ring. These hemins are abbreviated as "long," "short," and "stiff" hemins, respectively. In the deoxy state, the iron-imidazole stretching frequencies [nu(Fe--N epsilon)] for long, short, and stiff hemins are detected at 200, 207, and 204 cm-1, respectively. The strain induced in the iron-imidazole bond by the short hemin results in a higher nu(Fe--N epsilon) frequency, in contrast to the strain induced by sterically hindered 2-methylimidazole or 1,2-dimethylimidazole complexes in which the Fe--N epsilon bond is tilted and lengthened, but the imidazole ring remains perpendicular to the heme plane. However, in the short hemin, the plane of the imidazole ring may not be perpendicular to the plane of the porphyrin, altering the amount of pi-interaction (hence the strength of Fe--N epsilon bond) and the nature of normal mode containing Fe--N epsilon bond stretching. Upon CO binding, we have observed the nu(Fe--CO) stretching frequencies at 497 (long), 499 (short), and 496 cm-1 (stiff), somewhat lower than those reported by Mitchell et al. (Inorg. Chem., 1985, 24:967) for the chelated-heme X CO complexes (i.e., 501-506 cm-1). This is the first report of an iron-oxygen-associated vibration observed in solution for an unprotected heme. The oxy complexes were formed by introducing dioxygen to the deoxy complexes at -700C. The isotope-sensitive line was detected at 576 cm- (1602) in oxy stiff hemin, which was shifted to 545 cm-1 upon 1802 substitution. This is perhaps the largest isotope shift (31 cm-') observed to date, compared with the usual 22-24 cm-'.For the long and short hemins, the iron-oxygen-associated vibration was detected at 574 and 573 cm-', respectively.These values are very similar to those observed(N-methylimidazole) and myoglobin/hemoglobin.

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Year:  1987        PMID: 3828461      PMCID: PMC1329889          DOI: 10.1016/S0006-3495(87)83334-9

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


  13 in total

1.  Resonance Raman studies of ligand binding.

Authors:  N T Yu
Journal:  Methods Enzymol       Date:  1986       Impact factor: 1.600

Review 2.  Regulation of oxygen affinity of hemoglobin: influence of structure of the globin on the heme iron.

Authors:  M F Perutz
Journal:  Annu Rev Biochem       Date:  1979       Impact factor: 23.643

3.  Solution behavior of a synthetic myoglobin active site.

Authors:  C K Chang; T G Traylor
Journal:  J Am Chem Soc       Date:  1973-08-22       Impact factor: 15.419

4.  Letter: Reversible oxygen adduct formation in ferrous complexes derived from a "picket fence" prophyrin. A model for oxymyoglobin.

Authors:  J P Collman; R R Gagne; T R Halbert; J C Marchon; C A Reed
Journal:  J Am Chem Soc       Date:  1973-11-14       Impact factor: 15.419

5.  Cyclophane porphyrin.

Authors:  H Dickmann; C K Chang; T G Traylor
Journal:  J Am Chem Soc       Date:  1971-08-11       Impact factor: 15.419

6.  Substituted deuteroporphyrins. IV. On the kinetics and mechanism of reactions of iron(II) porphyrins with oxygen.

Authors:  I A Cohen; W S Caughey
Journal:  Biochemistry       Date:  1968-02       Impact factor: 3.162

7.  Absence of heme-localized strain in T state hemoglobin: insensitivity of heme-imidazole resonance Raman frequencies to quaternary structure.

Authors:  J Kincaid; P Stein; T G Spiro
Journal:  Proc Natl Acad Sci U S A       Date:  1979-02       Impact factor: 11.205

8.  Resonance Raman studies of carbon monoxide binding to iron "picket fence" porphyrin with unhindered and hindered axial bases. An inverse relationship between binding affinity and the strength of iron-carbon bond.

Authors:  E A Kerr; H C Mackin; N T Yu
Journal:  Biochemistry       Date:  1983-09-13       Impact factor: 3.162

9.  Resonance Raman investigation of carbon monoxide bonding in (carbon monoxy)hemoglobin and -myoglobin: detection of Fe-CO stretching and Fe-C-O bending vibrations and influence of the quaternary structure change.

Authors:  M Tsubaki; R B Srivastava; N T Yu
Journal:  Biochemistry       Date:  1982-03-16       Impact factor: 3.162

10.  Resonance Raman studies of Co-O2 and O-O stretching vibrations in oxy-cobalt hemes.

Authors:  H C Mackin; M Tsubaki; N T Yu
Journal:  Biophys J       Date:  1983-03       Impact factor: 4.033

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  1 in total

1.  New perspectives on iron-ligand vibrations of oxyheme complexes.

Authors:  Jianfeng Li; Qian Peng; Alexander Barabanschikov; Jeffrey W Pavlik; E Ercan Alp; Wolfgang Sturhahn; Jiyong Zhao; Charles E Schulz; J Timothy Sage; W Robert Scheidt
Journal:  Chemistry       Date:  2011-08-29       Impact factor: 5.236

  1 in total

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