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短的、带电荷的肽标签的掺入会影响带正电荷的弹性蛋白样多肽的温度响应性。

Incorporation of short, charged peptide tags affects the temperature responsiveness of positively-charged elastin-like polypeptides.

机构信息

Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN 47907, USA.

出版信息

J Mater Chem B. 2019 Sep 14;7(34):5245-5256. doi: 10.1039/c9tb00821g. Epub 2019 Aug 6.

Abstract

Elastin-like polypeptides (ELPs) are recombinant protein domains exhibiting lower critical solution temperature (LCST) behavior. This LCST behavior is controlled not only by intrinsic factors including amino acid composition and polypeptide chain length but also by non-ELP fusion domains. Here, we report that the presence of a composite non-ELP sequence that includes both His and T7 tags or a short Ser-Lys-Gly-Pro-Gly (SKGPG) sequence can dramatically change the LCST behavior of a positively-charged ELP domain. Both the His and T7 tags have been widely used in recombinant protein design to enable affinity chromatography and serve as epitopes for protein detection. The SKGPG sequence has been used to improve the expression of ELPs. Both the composite tag and the SKGPG sequence are <15% of the total length of the ELP fusion proteins. Despite the small size of the composite tag, its incorporation imparted pH-sensitive LCST behavior to the positively-charged ELP fusion protein. This pH sensitivity was not observed with the incorporation of the SKGPG sequence. The pH sensitivity results from both electrostatic and hydrophobic interactions between the composite tag and the positively-charged ELP domain. The hydrophobicity of the composite tag also alters the ELP interaction with Hofmeister salts by changing the overall hydrophobicity of the fusion protein. Our results suggest that incorporation of short tag sequences should be considered when designing temperature-responsive ELPs and provide insights into utilizing both electrostatic and hydrophobic interactions to design temperature-responsive recombinant proteins as well as synthetic polymers.

摘要

弹性蛋白样多肽(ELPs)是具有较低临界溶液温度(LCST)行为的重组蛋白结构域。这种 LCST 行为不仅受到包括氨基酸组成和多肽链长度在内的内在因素的控制,还受到非 ELP 融合结构域的控制。在这里,我们报告说,存在包含 His 和 T7 标签或短的 Ser-Lys-Gly-Pro-Gly(SKGPG)序列的复合非 ELP 序列可以极大地改变带正电荷的 ELP 结构域的 LCST 行为。His 和 T7 标签已广泛用于重组蛋白设计,以实现亲和层析,并作为蛋白质检测的表位。SKGPG 序列已被用于提高 ELP 的表达。复合标签和 SKGPG 序列均<ELP 融合蛋白总长度的 15%。尽管复合标签的尺寸很小,但它的掺入赋予了带正电荷的 ELP 融合蛋白 pH 敏感的 LCST 行为。在掺入 SKGPG 序列时未观察到这种 pH 敏感性。这种 pH 敏感性源于复合标签与带正电荷的 ELP 结构域之间的静电和疏水相互作用。复合标签的疏水性还通过改变融合蛋白的整体疏水性来改变 ELP 与 Hofmeister 盐的相互作用。我们的结果表明,在设计温度响应性 ELP 时应考虑短标签序列的掺入,并为利用静电和疏水相互作用设计温度响应性重组蛋白以及合成聚合物提供了见解。

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