Goszczyński Tomasz Marek, Gawłowski Maciej, Girek Beata, Kowalski Konrad, Boratyński Janusz, Girek Tomasz
Laboratory of Biomedical Chemistry, Department of Experimental Oncology, Hirszfeld Institute of Immunology and Experimental Therapy, PAS, 12 Rudolf Weigl St., 53-114 Wrocław, Poland.
Institute of Chemistry, Environmental Protection and Biotechnology, Jan Dlugosz University, Armii Krajowej Ave., 13/15, 42 201 Częstochowa, Poland.
J Incl Phenom Macrocycl Chem. 2017;87(3):341-348. doi: 10.1007/s10847-017-0706-8. Epub 2017 Mar 8.
Recently a great interest in the field of protein engineering and the design of innovative drug delivery systems employing specific ligands such as cyclodextrins is observed. The paper reports the solid state, thermal method for protein coupling with β-cyclodextrin and the physicochemical and biological properties of the obtained conjugates. The structure of the obtained conjugates was investigated via liquid chromatography-mass spectrometry, dynamic light scattering and circular dichroism analysis. The presented conjugates were biologically active and covalently bound β-cyclodextrin preserved the ability to form inclusion complexes with the model compound. This report demonstrates the great potential of cyclodextrin as a modifying unit that can be used to modulate the properties of therapeutic proteins, additionally giving such conjugates the possibility to transport many therapeutic substances in the form of inclusion complexes. In addition, the paper presents the potential of protein-cyclodextrin conjugates to construct innovative bioactive molecules for biological and medical applications.
最近,人们对蛋白质工程领域以及采用环糊精等特定配体的创新药物递送系统的设计产生了浓厚兴趣。本文报道了蛋白质与β-环糊精偶联的固态热方法以及所得缀合物的物理化学和生物学性质。通过液相色谱-质谱、动态光散射和圆二色性分析研究了所得缀合物的结构。所呈现的缀合物具有生物活性,共价结合的β-环糊精保留了与模型化合物形成包合物的能力。本报告证明了环糊精作为一种修饰单元的巨大潜力,可用于调节治疗性蛋白质的性质,此外还使此类缀合物有可能以包合物的形式运输许多治疗物质。此外,本文还介绍了蛋白质-环糊精缀合物构建用于生物学和医学应用的创新生物活性分子的潜力。