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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Escherichia coli OmpA retains a folded structure in the presence of sodium dodecyl sulfate due to a high kinetic barrier to unfolding
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Escherichia coli OmpA retains a folded structure in the presence of sodium dodecyl sulfate due to a high kinetic barrier to unfolding

机译:大肠杆菌OmpA在十二烷基硫酸钠存在的情况下保留了折叠结构,这是由于其对展开具有很高的动力学屏障

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摘要

Escherichia coli OmpA can be solubilized by sodium dodecyl sulfate (SDS) in its folded structure, and it unfolds upon heating. Although the heat-denatured OmpA remains unfolded after lowering the temperature, the addition of a non-ionic surfactant, octyl glucoside results in refolding of unfolded OmpA. In the present study, we investigated the refolding kinetics of OmpA in a mixed surfactant system of SDS and octyl glucoside using far- and near-UV circular dichroism and fluorescence spectroscopies. We found four kinetic phases in the refolding reaction, which logarithmically depended on the weight fraction of octyl glucoside. We also examined the unfolding kinetics of OmpA upon heating in the presence of SDS by temperature jump experiments. A comparison of the rate constants for the refolding and the unfolding reactions in SDS-only solution at 30 ℃ revealed that the folded form of OmpA in SDS solution is less table than the unfolding form, and that the unfolding is virtually unobservable near room temperature due to a high kinetic barrier.
机译:大肠杆菌OmpA可以用折叠结构的十二烷基硫酸钠(SDS)溶解,并在加热时展开。尽管降低温度后,热变性的OmpA仍保持未折叠状态,但添加非离子型表面活性剂辛基葡糖苷会导致未折叠的OmpA重新折叠。在本研究中,我们使用远紫外和近紫外圆二色性和荧光光谱研究了SDS和辛基葡糖苷混合表面活性剂系统中OmpA的重折叠动力学。我们在重折叠反应中发现了四个动力学相,其对数依赖于辛基葡萄糖苷的重量分数。我们还通过温度跳跃实验研究了在SDS存在下加热时OmpA的展开动力学。比较在30℃下仅SDS溶液中重折叠和展开反应的速率常数,发现OmpA在SDS溶液中的折叠形式比展开形式要小,并且在室温附近,这种展开实际上是观察不到的。高的动力学屏障。

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