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M C Symons

Publications and source records attributed to M C Symons.

11 recordsLinked to original sources
PubMed1992

Biological methane activation involves the intermediacy of carbon-centered radicals.

The spin-trapping technique has demonstrated that carbon-centered radicals are produced during soluble-methane-monooxygenase catalysis of the hydroxylation of several different types of substrate. The resulting spin-adducts were identified from the hyperfine splitting constants in their EPR spectra. Isotopic labelling showed unequivocally that the trapped radicals were derived from substrate. The carbon-centered substrate radicals are believed to result from hydrogen-atom abstraction by a ferryl species in a cytochrome-P-450-like mechanism. No hydroxy radical nor an oxygen-based radical of any kind was detected in any of the spin-trapping experiments.

Carbon↗
PubMed1989

Effect of ionizing radiation on haemoglobin: the oxy-derivative of haemoglobin Iwate.

It is well established that exposure of oxyhaemoglobin to ionizing radiation results in remarkably selective electron addition to the (FeO2) unit, giving a novel species, (FeO2)-, in which the extra electron is largely localized on iron and dioxygen. This work has now been extended to haemoglobin (Hb.) Iwate. The haemoglobin M. Iwate used is a mutant haemoglobin having only Fe(III) alpha-chains by oxy beta-chains (alpha 2 Met beta 2 oxy). The haem iron atoms in the alpha-chains are coordinated in the fifth site by a proximal tyrosine in place of histidine. This unit is a high-spin Fe(III) with axial symmetry and prominent electron spin resonance (ESR) features in the g = 6 and g = 2 regions. On exposure to 60Co gamma-rays at 77 K, efficient electron addition occurred at both types of iron centre, giving Fe(II) and (FeO2)- units. The former was monitored by the decrease of the g = 6 feature for Fe(III) and the latter by the growth of g-features at 2.254 (gx), 2.149 (gy) and 1.967 (gz). These values are close to those for the FeO2- centre formed in the beta-chains of normal oxyhaemoglobin. On annealing above 77 K, two changes occurred: first there was a small but clear increase in gx and gy, followed by a marked reduction in gx and gy giving g-values close to those for the centre formed directly in the alpha-chains of the normal protein. Finally, this intermediate species gave a centre having gx = 2.310, gy = 2.180 and gz = 1.935. These values are typical of low-spin Fe(III) haemoglobin and are assigned to the protonated complex, Fe(III)O2H. Ultimately at ca. room temperature, this was converted into the high-spin, met-form, with a gain in the g = 6 feature. These results established that the beta-chain centre in Hb. Iwate behave in the same way as isolated beta-chains. They also confirm that electron addition to the oxy-units is facile, even in the presence of Fe(III) units in each tetramer. The results also confirm that electron capture to give (FeO2)- units is not followed by internal electron-transfer to give Fe(II) from the Fe(III) centres in the alpha-chains.

Cobalt Radioisotopes↗
PubMed1978

The relative electron affinities of the alpha and beta chains of oxyhaemoglobin as a function of pH and added inositol hexaphosphate. An electron spin resonance study.

Exposure of aqueous glasses of oxyhaemoglobin to 60Co gamma-rays at 77K results in electron addition to the FeO2 unit, the ESR spectrum for the alpha-chain electron adduct being well separated from that for the beta-chain. The relative yields of these two centres has been measured in the pH range 4.5 to 8.5, with or without added inositol hexaphosphate. We find that, in the absence of inositol hexaphosphate, the yield of beta-chain adduct is almost equal to that of the alpha-chains in the pH 4--5 region, but these rapidly diverge with increasing pH, the beta-yield increasing and the alpha-yield decreasing. After a plateau in the pH 6--8 region, the yield of beta-chain adduct decreases, but that of the alpha-chain adduct remains constant. In the presence of an excess of inositol hexaphosphate the pH change for the beta-adduct remains, but at low pH values the yield of the alpha-adduct is much greater than that of the beta-adduct. This constraint is removed with a pK of approx. 7.7 and at high pH values the yield of the beta-adduct is once again greater than that of the alpha-adduct. These results are significant in that they suggest that the electron affinities of the alpha and beta chains in oxyhaemoglobin are a function of pH, with that of the beta-chains being greater than that of the alpha-chains in the neutral region. Also inositol hexaphosphate clearly binds to one or both chains, and this has the effect of reversing the relative electron affinities of the two chains.

Electron Spin Resonance Spectroscopy↗
PubMed1978

Electron capture at the iron-oxygen centre in single crystals of oxymyoglobin studied by electron spin resonance spectroscopy.

Exposure of single crystals of oxy-myoglobin to 60Co gamma-rays at 77 K results in electron addition to the Fe-O2 units. The resulting ESR spectrum has been analysed to give the principal values and directions for the g-tensor of this unit. The results suggest that the dioxygen ligand is strongly tilted, the direction of tilt being close to one of the bisectors of the N-Fe-N bond angles. Possible reasons for this orientation are discussed.

Chemical Phenomena↗
PubMed1978

Electron addition to the active site of Cancer magister haemocyanins. An ESR study of cu(II) centres after gamma-radiolysis.

Exposure of aqueous glasses of Cancer magister haemocyanin to 60Co gamma-rays at 77 K results in a novel paramagnetic centre with ESR features showing hyperfine coupling to one strongly coupled 63/65 Cu nucleus and possibly one weakly interacting 63/65 Cu nucleus. Addition of electron scavengers showed that this centre is formed by electron addition. It is suggested that addition occurs at Cu2+-O2-Cu2+ units to give Cu2+-O2Cu+ centres. If this is correct, then electron-transfer between the two copper ions is slow or non-existent, possibly indicating that they are inequivalent. The centre is unstable, the signals being lost irreversibly on heating to approx. 270 K. The g parallel and A parallel (63/65Cu) data place this centre into the type I classification.

Animals↗
PubMed1975

Water structure and hydration.

Possible structures adopted by bulk water are discussed with special reference to the possible presence of monomeric water and the detection of 'free' -OH groups. The way in which water tends to accommodate small hydrophobic molecules is considered, with particular reference to the clathrate theory and the phenomenon of 'structure making'. Cage-pairing and cage-sharing processes are described. Consideration of the way water solvates cations and anions is followed by a discussion of the way these solvated ions interact with the bulk medium. Large symmetrical alkylammonium ions probably encourage clathrate cage formation, at least at low temperatures. Particular reference is made to the use of infrared, Raman, ultraviolet, n.m.r. and e.s.r. spectroscopic techniques to the study of water and aqueous solutions.

Chemical Phenomena↗
PubMedDate not supplied

Sulphur radicals formed by cutting alpha-keratin.

Finger nails are composed largely of alpha-keratin, a protein in which three right-handed alpha-helical peptide chains are twisted into a left-handed coil strengthened by disulphide cross links. We have found that the act of cutting nails generates trapped radicals, giving intense electron spin resonance (ESR) signals characteristic of sulphur centred radicals. The nature of the primary radical and the possible modes of generation are discussed. These radical reactions should be considered when using human nail parings to estimate accidental exposure to ionizing radiation.

Disulfides↗