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丝氨酸蛋白酶抑制剂——用于修饰聚合生物材料的新型分子。

Serine Protease Inhibitors-New Molecules for Modification of Polymeric Biomaterials.

机构信息

Department of Biochemistry and Biotechnology, Maria Curie-Skłodowska University, Akademicka 19, 20-033 Lublin, Poland.

Department of Functional Anatomy and Cytobiology, Maria Curie-Skłodowska University, Akademicka 19, 20-033 Lublin, Poland.

出版信息

Biomolecules. 2020 Jan 4;10(1):82. doi: 10.3390/biom10010082.

Abstract

Three serine protease inhibitors (AEBSF, soy inhibitor, α-antitrypsin) were covalently immobilized on the surface of three polymer prostheses with the optimized method. The immobilization efficiency ranged from 11 to 51%, depending on the chosen inhibitor and biomaterial. The highest activity for all inhibitors was observed in the case of immobilization on the surface of the polyester Uni-Graft prosthesis, and the preparations obtained showed high stability in the environment with different pH and temperature values. Modification of the Uni-Graft prosthesis surface with the synthetic AEBSF inhibitor and human α-antitrypsin inhibited the adhesion and multiplication of subs. and from the collection of the Department of Genetics and Microbiology, UMCS. Optical profilometry analysis indicated that, after the immobilization process on the surface of AEBSF-modified Uni-Graft prostheses, there were more structures with a high number of protrusions, while the introduction of modifications with a protein inhibitor led to the smoothing of their surface.

摘要

三种丝氨酸蛋白酶抑制剂(AEBSF、大豆抑制剂、α-抗胰蛋白酶)通过优化的方法被共价固定在三种聚合物假体的表面。固定效率取决于所选抑制剂和生物材料,范围在 11%到 51%之间。对于所有抑制剂来说,在聚酯 Uni-Graft 假体表面固定时观察到的活性最高,并且获得的制剂在不同 pH 值和温度值的环境中表现出高稳定性。用合成的 AEBSF 抑制剂和人α-抗胰蛋白酶修饰 Uni-Graft 假体表面抑制了 来自遗传学和微生物学系收集的 sub. 和 sub.。光学轮廓分析表明,在 AEBSF 修饰的 Uni-Graft 假体表面进行固定化过程后,有更多的具有大量突出物的结构,而用蛋白质抑制剂进行修饰则导致其表面变得平滑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acab/7023003/4594408c42e6/biomolecules-10-00082-g0A1.jpg

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