Lamb Don C, Nienhaus Karin, Arcovito Alessandro, Draghi Federica, Miele Adriana E, Brunori Maurizio, Nienhaus G Ulrich
Department of Biophysics, University of Ulm, D-89069 Ulm, Germany.
J Biol Chem. 2002 Apr 5;277(14):11636-44. doi: 10.1074/jbc.M109892200. Epub 2002 Jan 15.
Fourier transform infrared (FTIR) spectroscopy in the CO stretch bands combined with temperature derivative spectroscopy (TDS) was used to characterize intermediate states obtained by photolysis of two sperm whale mutant myoglobins, YQR (L29(B10)Y, H64(E7)Q, T67(E10)R) and YQRF (with an additional I107(G8)F replacement). Both mutants assume two different bound-state conformations, A(0) and A(3), which can be distinguished by their different CO bands near 1965 and 1933 cm(-1). They most likely originate from different conformations of the Gln-64 side chain. Within each A substate, a number of photoproduct states have been characterized on the basis of the temperature dependence of recombination in TDS experiments. Different locations and orientations of the ligand within the protein can be distinguished by the infrared spectra of the photolyzed CO. Recombination from the primary docking site, B, near the heme dominates below 50 K. Above 60 K, ligand rebinding occurs predominantly from a secondary docking site, C', in which the CO is trapped in the Xe4 cavity on the distal side, as shown by crystallography of photolyzed YQR and L29W myoglobin CO. Another kinetic state (C") has been identified from which rebinding occurs around 130 K. Moreover, a population appearing above the solvent glass transition at approximately 180 K (D state) is assigned to rebinding from the Xe1 cavity, as suggested by the photoproduct structure of the L29W sperm whale myoglobin mutant. For both the YQR and YQRF mutants, rebinding from the B sites near the heme differs for the two A substates, supporting the view that the return of the ligand from the C', C", and D states is not governed by the recombination barrier at the heme iron but rather by migration to the active site. Comparison of YQR and YQRF shows that access to the Xe4 site (C') is severely restricted by introduction of the bulky Phe side chain at position 107.
傅里叶变换红外(FTIR)光谱在CO伸缩带与温度导数光谱(TDS)相结合的情况下,用于表征通过光解两种抹香鲸突变肌红蛋白YQR(L29(B10)Y、H64(E7)Q、T67(E10)R)和YQRF(额外有I107(G8)F替换)所获得的中间态。这两种突变体都呈现出两种不同的结合态构象,A(0)和A(3),可通过它们在1965和1933 cm⁻¹附近不同的CO带来区分。它们很可能源自Gln - 64侧链的不同构象。在每个A子态内,基于TDS实验中重组的温度依赖性,已经对许多光产物态进行了表征。蛋白质内配体的不同位置和取向可通过光解后的CO的红外光谱来区分。在50 K以下,来自靠近血红素的主要对接位点B的重组占主导。在60 K以上,配体重新结合主要发生在二级对接位点C',如光解后的YQR和L29W肌红蛋白CO的晶体学所示,其中CO被困在远端的Xe4腔内。已经确定了另一种动力学态(C"),在约130 K左右发生重新结合。此外,如L29W抹香鲸肌红蛋白突变体的光产物结构所暗示的,在约180 K的溶剂玻璃化转变温度以上出现的一个群体(D态)被归因于从Xe1腔的重新结合。对于YQR和YQRF突变体,两种A子态中来自血红素附近B位点的重新结合有所不同,支持了这样一种观点,即配体从C'、C"和D态的返回不是由血红素铁处的重组屏障决定,而是由向活性位点的迁移决定。YQR和YQRF的比较表明,在位置107引入庞大的苯丙氨酸侧链会严重限制进入Xe4位点(C')。