TY - JOUR
T1 - The source of heterogeneity in the heme vicinity of ferricytochrome c
AU - Taler, Galia
AU - Becker, Oren M.
AU - Navon, Gil
AU - Qin, Wenying
AU - Margoliash, Emanuel
AU - Schejter, Abel
PY - 1999/6/28
Y1 - 1999/6/28
N2 - Heterogeneity in the heme vicinity of ferricytochrome c was reported to be detectable by a split of the NMR signal of the heme methyl 3 group [P.D. Burns and G.N. La Mar, J. Am. Chem. Soc. 101 (1979) 5844]. Using cytochrome c mutants and computer simulations of the native and mutated cytochromes, the source of this heterogeneity is found to originate from the His-33 residue motions. The H33F mutation abolished the NMR split and computer simulations of the H33F mutant revealed a narrower distribution of fluctuations of the radius of gyration, suggesting a more rigid structure due to the mutation. The stabilization of the mutant was further demonstrated by a reduction in the H33F mutant of 4 Kcal/mol in the calculated interaction energy between residue 33 and the rest of the cytochrome, in keeping with known experimental results [W. Qin, R. Sanishvili, B. Plotkin, A. Schejter and E. Margoliash, Biochim. Biophys. Acta 1252 (1995) 87]. Copyright (C) 1999 Elsevier Science B.V.
AB - Heterogeneity in the heme vicinity of ferricytochrome c was reported to be detectable by a split of the NMR signal of the heme methyl 3 group [P.D. Burns and G.N. La Mar, J. Am. Chem. Soc. 101 (1979) 5844]. Using cytochrome c mutants and computer simulations of the native and mutated cytochromes, the source of this heterogeneity is found to originate from the His-33 residue motions. The H33F mutation abolished the NMR split and computer simulations of the H33F mutant revealed a narrower distribution of fluctuations of the radius of gyration, suggesting a more rigid structure due to the mutation. The stabilization of the mutant was further demonstrated by a reduction in the H33F mutant of 4 Kcal/mol in the calculated interaction energy between residue 33 and the rest of the cytochrome, in keeping with known experimental results [W. Qin, R. Sanishvili, B. Plotkin, A. Schejter and E. Margoliash, Biochim. Biophys. Acta 1252 (1995) 87]. Copyright (C) 1999 Elsevier Science B.V.
KW - Cytochrome c chemistry
KW - H33F mutant
KW - Molecular dynamics
KW - NMR
UR - http://www.scopus.com/inward/record.url?scp=0033612558&partnerID=8YFLogxK
U2 - 10.1016/S0301-4622(99)00040-X
DO - 10.1016/S0301-4622(99)00040-X
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AN - SCOPUS:0033612558
SN - 0301-4622
VL - 79
SP - 193
EP - 197
JO - Biophysical Chemistry
JF - Biophysical Chemistry
IS - 3
ER -