Literature DB >> 20815568

Absorption in the Q-band region by isolated ferric heme+ and heme+(histidine) in vacuo.

Jean Ann Wyer1, Steen Brøndsted Nielsen.   

Abstract

Absorption by heme proteins is determined by the heme microenvironment that is often vacuumlike (hydrophobic pocket). Here we provide absorption spectra in the Q-band region of isolated ferric heme(+) and heme(+)(histidine) ions in vacuo to be used as references in protein biospectroscopy. Ions were photoexcited in an electrostatic storage ring and their decay monitored in time. Both ions display a triple band structure with maxima at 500, 518, and 530 nm. Previous attempts to study four-coordinate Fe(III)-heme(+) were hampered by the strong affinity of Fe(3+) for water and anions. Absorption at higher wavelengths is also measured, which is ascribed to charge-transfer transitions from the porphyrin to the iron. Finally, our data serve to benchmark theoretical calculations.

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Year:  2010        PMID: 20815568     DOI: 10.1063/1.3474998

Source DB:  PubMed          Journal:  J Chem Phys        ISSN: 0021-9606            Impact factor:   3.488


  1 in total

1.  Ion Mobility Measurements of Multianionic Metalloporphyrin Dimers: Structural Changes Induced by Countercation Exchange.

Authors:  Erik Schneider; Katrina Brendle; Patrick Jäger; Patrick Weis; Manfred M Kappes
Journal:  J Am Soc Mass Spectrom       Date:  2018-04-17       Impact factor: 3.109

  1 in total

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