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蝎子毒素更喜欢盐溶液。

Scorpion toxins prefer salt solutions.

作者信息

Nikouee Azadeh, Khabiri Morteza, Cwiklik Lukasz

机构信息

Institute of Applied Physiology, Ulm University, Ulm, Germany.

Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, 16610, Prague 6, Czech Republic.

出版信息

J Mol Model. 2015 Nov;21(11):287. doi: 10.1007/s00894-015-2822-y. Epub 2015 Oct 16.

Abstract

There is a wide variety of ion channel types with various types of blockers, making research in this field very complicated. To reduce this complexity, it is essential to study ion channels and their blockers independently. Scorpion toxins, a major class of blockers, are charged short peptides with high affinities for potassium channels. Their high selectivity and inhibitory properties make them an important pharmacological tool for treating autoimmune or nervous system disorders. Scorpion toxins typically have highly charged surfaces and-like other proteins-an intrinsic ability to bind ions (Friedman J Phys Chem B 115(29):9213-9223, 1996; Baldwin Biophys J 71(4):2056-2063, 1996; Vrbka et al. Proc Natl Acad Sci USA 103(42):15440-15444, 2006a; Vrbka et al. J Phys Chem B 110(13):7036-43, 2006b). Thus, their effects on potassium channels are usually investigated in various ionic solutions. In this work, computer simulations of protein structures were performed to analyze the structural properties of the key residues (i.e., those that are presumably involved in contact with the surfaces of the ion channels) of 12 scorpion toxins. The presence of the two most physiologically abundant cations, Na(+) and K(+), was considered. The results indicated that the ion-binding properties of the toxin residues vary. Overall, all of the investigated toxins had more stable structures in ionic solutions than in water. We found that both the number and length of elements in the secondary structure varied depending on the ionic solution used (i.e., in the presence of NaCl or KCl). This study revealed that the ionic solution should be chosen carefully before performing experiments on these toxins. Similarly, the influence of these ions should be taken into consideration in the design of toxin-based pharmaceuticals.

摘要

离子通道类型繁多,且存在各种类型的阻滞剂,这使得该领域的研究非常复杂。为了降低这种复杂性,独立研究离子通道及其阻滞剂至关重要。蝎毒素是一类主要的阻滞剂,是带电荷的短肽,对钾通道具有高亲和力。它们的高选择性和抑制特性使其成为治疗自身免疫性或神经系统疾病的重要药理学工具。蝎毒素通常具有高度带电的表面,并且与其他蛋白质一样,具有结合离子的内在能力(弗里德曼《物理化学杂志B》115(29):9213 - 9223,1996;鲍德温《生物物理杂志》71(4):2056 - 2063,1996;弗尔布卡等人《美国国家科学院院刊》103(42):15440 - 15444,2006a;弗尔布卡等人《物理化学杂志B》110(13):7036 - 43,2006b)。因此,通常在各种离子溶液中研究它们对钾通道的影响。在这项工作中,进行了蛋白质结构的计算机模拟,以分析12种蝎毒素关键残基(即推测参与与离子通道表面接触的残基)的结构特性。考虑了两种生理上最丰富的阳离子Na(+)和K(+)的存在。结果表明,毒素残基的离子结合特性各不相同。总体而言,所有研究的毒素在离子溶液中的结构比在水中更稳定。我们发现二级结构中元件的数量和长度都因所用的离子溶液(即存在NaCl或KCl)而异。这项研究表明,在对这些毒素进行实验之前应仔细选择离子溶液。同样,在基于毒素的药物设计中应考虑这些离子的影响。

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