Sebban-Kreuzer C, Blanchard L, Bersch B, Blackledge M J, Marion D, Dolla A, Guerlesquin F
Unité de Bioénergétique et Ingénierie des Protéines, IBSM-CNRS, Marseille, France.
Eur J Biochem. 1998 Feb 1;251(3):787-94. doi: 10.1046/j.1432-1327.1998.2510787.x.
Y64 has been replaced in cytochrome c553 from Desulfovibrio vulgaris Hildenborough by phenylalanine, leucine, valine, serine and alanine residues. An NMR study of structural variation induced in both oxidoreduction states of the molecule has been carried out by analysing observed chemical-shift variations. Dynamic changes were evidenced using NH exchange. We have observed that the substitution has a drastic effect on the stability of the molecule in the reduced state, although there is no effect on the reduction potential of the cytochrome. Y64-->F substitution induces particular effects on the NH exchange at the N-terminal, C-terminal and central alpha-helices and increases the stability of the oxidized molecule.
在来自希登伯勒脱硫弧菌的细胞色素c553中,Y64已被苯丙氨酸、亮氨酸、缬氨酸、丝氨酸和丙氨酸残基取代。通过分析观察到的化学位移变化,对该分子两种氧化还原状态下诱导的结构变化进行了核磁共振研究。利用NH交换证明了动态变化。我们观察到,尽管这种取代对细胞色素的还原电位没有影响,但对还原态分子的稳定性有显著影响。Y64→F取代对N端、C端和中央α螺旋处的NH交换产生特殊影响,并增加了氧化态分子的稳定性。