Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin.

The kinetic properties of the three taxonomic A substates of sperm whale carbonmonoxy myoglobin in 75% glycerol/buffer are studied by flash photolysis with monitoring in the infrared stretch bands of bound CO at nu(A0) approximately 1967 cm-1, nu(A1) approximately 1947 cm-1, and nu(A3) approximately...

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Main Authors: Johnson, J B, Lamb, D C, Frauenfelder, H, Müller, J D, McMahon, B, Nienhaus, G U, Young, R D
Format: Text
Language:English
Published: 1996
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1233623
http://www.ncbi.nlm.nih.gov/pubmed/8874030
id ftpubmed:oai:pubmedcentral.nih.gov:1233623
record_format openpolar
spelling ftpubmed:oai:pubmedcentral.nih.gov:1233623 2023-05-15T18:26:53+02:00 Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin. Johnson, J B Lamb, D C Frauenfelder, H Müller, J D McMahon, B Nienhaus, G U Young, R D 1996-09 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1233623 http://www.ncbi.nlm.nih.gov/pubmed/8874030 en eng http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1233623 http://www.ncbi.nlm.nih.gov/pubmed/8874030 Research Article Text 1996 ftpubmed 2013-08-30T14:45:13Z The kinetic properties of the three taxonomic A substates of sperm whale carbonmonoxy myoglobin in 75% glycerol/buffer are studied by flash photolysis with monitoring in the infrared stretch bands of bound CO at nu(A0) approximately 1967 cm-1, nu(A1) approximately 1947 cm-1, and nu(A3) approximately 1929 cm-1 between 60 and 300 K. Below 160 K the photodissociated CO rebinds from the heme pocket, no interconversion among the A substates is observed, and rebinding in each A substate is nonexponential in time and described by a different temperature-independent distribution of enthalpy barriers with a different preexponential. Measurements in the electronic bands, e.g., the Soret, contain contributions of all three A substates and can, therefore, be only approximately modeled with a single enthalpy distribution and a single preexponential. The bond formation step at the heme is fastest for the A0 substate, intermediate for the A1 substate, and slowest for A3. Rebinding between 200 and 300 K displays several processes, including geminate rebinding, rebinding after ligand escape to the solvent, and interconversion among the A substates. Different kinetics are measured in each of the A bands for times shorter than the characteristic time of fluctuations among the A substates. At longer times, fluctuational averaging yields the same kinetics in all three A substates. The interconversion rates between A1 and A3 are determined from the time when the scaled kinetic traces of the two substates merge. Fluctuations between A1 and A3 are much faster than those between A0 and either A1 or A3, so A1 and A3 appear as one kinetic species in the exchange with A0. The maximum-entropy method is used to extract the distribution of rate coefficients for the interconversion process A0 <--> A1 + A3 from the flash photolysis data. The temperature dependencies of the A substate interconversion processes are fitted with a non-Arrhenius expression similar to that used to describe relaxation processes in glasses. At 300 K the ... Text Sperm whale PubMed Central (PMC)
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Research Article
spellingShingle Research Article
Johnson, J B
Lamb, D C
Frauenfelder, H
Müller, J D
McMahon, B
Nienhaus, G U
Young, R D
Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin.
topic_facet Research Article
description The kinetic properties of the three taxonomic A substates of sperm whale carbonmonoxy myoglobin in 75% glycerol/buffer are studied by flash photolysis with monitoring in the infrared stretch bands of bound CO at nu(A0) approximately 1967 cm-1, nu(A1) approximately 1947 cm-1, and nu(A3) approximately 1929 cm-1 between 60 and 300 K. Below 160 K the photodissociated CO rebinds from the heme pocket, no interconversion among the A substates is observed, and rebinding in each A substate is nonexponential in time and described by a different temperature-independent distribution of enthalpy barriers with a different preexponential. Measurements in the electronic bands, e.g., the Soret, contain contributions of all three A substates and can, therefore, be only approximately modeled with a single enthalpy distribution and a single preexponential. The bond formation step at the heme is fastest for the A0 substate, intermediate for the A1 substate, and slowest for A3. Rebinding between 200 and 300 K displays several processes, including geminate rebinding, rebinding after ligand escape to the solvent, and interconversion among the A substates. Different kinetics are measured in each of the A bands for times shorter than the characteristic time of fluctuations among the A substates. At longer times, fluctuational averaging yields the same kinetics in all three A substates. The interconversion rates between A1 and A3 are determined from the time when the scaled kinetic traces of the two substates merge. Fluctuations between A1 and A3 are much faster than those between A0 and either A1 or A3, so A1 and A3 appear as one kinetic species in the exchange with A0. The maximum-entropy method is used to extract the distribution of rate coefficients for the interconversion process A0 <--> A1 + A3 from the flash photolysis data. The temperature dependencies of the A substate interconversion processes are fitted with a non-Arrhenius expression similar to that used to describe relaxation processes in glasses. At 300 K the ...
format Text
author Johnson, J B
Lamb, D C
Frauenfelder, H
Müller, J D
McMahon, B
Nienhaus, G U
Young, R D
author_facet Johnson, J B
Lamb, D C
Frauenfelder, H
Müller, J D
McMahon, B
Nienhaus, G U
Young, R D
author_sort Johnson, J B
title Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin.
title_short Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin.
title_full Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin.
title_fullStr Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin.
title_full_unstemmed Ligand binding to heme proteins. VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin.
title_sort ligand binding to heme proteins. vi. interconversion of taxonomic substates in carbonmonoxymyoglobin.
publishDate 1996
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1233623
http://www.ncbi.nlm.nih.gov/pubmed/8874030
genre Sperm whale
genre_facet Sperm whale
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1233623
http://www.ncbi.nlm.nih.gov/pubmed/8874030
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