Guanidinium chloride induced unfolding of a hemocyanin subunit from Carcinus aestuarii

Roberto Favilla , Matteo Goldoni , Alberto Mazzini , Paolo Di Muro , Benedetto Salvato , Mariano Beltramini
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引用次数: 16

Abstract

The effects of guanidinium chloride (GuHCl) on the stability of the apo form of the 5S non-reassociating subunit of hemocyanin from the crab Carcinus aestuarii (apo-CaeSS2) were investigated, using a variety of optical spectroscopy techniques (light scattering (LS), fluorescence (IF and EF) and circular dichroism (CD)). The fluorescence of 8-anilino-1-naphtalene sulphonate (ANS) was strongly enhanced in the presence of apo-CaeSS2, in contast to holo-CaeSS2, suggesting the formation of a molten globule (MG)-like state, consequent to the removal of the two copper ions from the holo subunit. Other evidences, favouring the presence of this state in apo-CaeSS2, derive from an enhanced quenching of intrinsic fluorescence (IF) by acrylamide, a higher sensibility towards aggregation and a higher IF with respect to deoxy holo-CaeSS2. Aggregation of apo-CaeSS2 below 1.2 M GuHCl was detected by LS, suggesting the formation of an aggregation-prone intermediate, called I1. Due to this effect, fluorescence and CD data could only be collected above that denaturant concentration. Both IF (protein) and EF (ANS) fluorescence data were best fitted by a two-state cooperative transition, occurring between the intermediate I1 and the unfolded state U, with C1/2 1.6–1.7 M. A similar two-state transition, with a slightly higher C1/2 value (1.9 M), was also inferred from far-UV CD data, suggesting the possible formation of another intermediate. Partial refolding of apo-CaeSS2 by dilution was found to occur above 1.2 M GuHCl, i.e. up to the level of I1, since at lower denaturant concentration protein aggregation took place, as also observed in unfolding. All thermodynamic parameters, derived from data above 1.2 M GuHCl, are therefore referred to transitions between intermediate and unfolded states only. Unfolding kinetics, followed by fluorescence stopped-flow, was biphasic in the whole GuHCl range investigated (3–5 M), suggesting the formation of a transient intermediate, possibly related to that observed under equilibrium conditions.

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氯化胍诱导河口癌血青素亚基展开
采用光散射(LS)、荧光(IF和EF)和圆二色性(CD)等多种光谱技术,研究了氯化胍(GuHCl)对aestuarii蟹血青素5S非再结合亚基(apo- caess2)载子形式稳定性的影响。与空心caess2相比,8-苯胺-1-萘磺酸钠(ANS)在apo-CaeSS2存在下的荧光明显增强,这表明由于空心亚基上的两个铜离子被去除,形成了熔化的球状(MG)态。其他证据表明,apo-CaeSS2中存在这种状态,这是由于丙烯酰胺增强了本征荧光(IF)的猝灭,对聚集的敏感性更高,对脱氧全息caess2的IF更高。LS检测到apo-CaeSS2在1.2 M GuHCl下聚集,表明形成了易于聚集的中间体I1。由于这种影响,荧光和CD数据只能在该变性剂浓度以上收集。IF (protein)和EF (ANS)的荧光数据最适合于发生在中间体I1和未折叠态U之间的两态合作跃迁,C1/2值为1.6-1.7 M。从远紫外CD数据中也推断出类似的两态跃迁,C1/2值略高(1.9 M),表明可能形成另一个中间体。通过稀释发现,apo-CaeSS2的部分再折叠发生在1.2 M GuHCl以上,即达到I1的水平,因为在较低的变性剂浓度下会发生蛋白质聚集,正如在展开中观察到的那样。因此,从1.2 M GuHCl以上的数据中得出的所有热力学参数仅涉及中间态和未展开态之间的转变。展开动力学,然后是荧光停止流动,在所研究的整个GuHCl范围内(3-5 M)是双相的,表明形成了一种瞬态中间体,可能与平衡条件下观察到的有关。
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