Sen-Britain Shohini, Hicks Wesley L, Hard Robert, Gardella Joseph A
Department of Chemistry, State University of New York at Buffalo, 475 Natural Sciences Complex, Buffalo, New York 14221.
Department of Head and Neck/Plastic and Reconstructive Surgery, Roswell Comprehensive Cancer Center, 665 Elm Street, Buffalo, New York 14203.
Biointerphases. 2018 Oct 25;13(6):06E406. doi: 10.1116/1.5051655.
The development of hydrogels for protein delivery requires protein-hydrogel interactions that cause minimal disruption of the protein's biological activity. Biological activity can be influenced by factors such as orientational accessibility for receptor binding and conformational changes, and these factors can be influenced by the hydrogel surface chemistry. (Hydroxyethyl)methacrylate (HEMA) hydrogels are of interest as drug delivery vehicles for keratinocyte growth factor (KGF) which is known to promote re-epithelialization in wound healing. The authors report here the surface characterization of three different HEMA hydrogel copolymers and their effects on the orientation and conformation of surface-bound KGF. In this work, they characterize two copolymers in addition to HEMA alone and report how protein orientation and conformation is affected. The first copolymer incorporates methyl methacrylate (MMA), which is known to promote the adsorption of protein to its surface due to its hydrophobicity. The second copolymer incorporates methacrylic acid (MAA), which is known to promote the diffusion of protein into its surface due to its hydrophilicity. They find that KGF at the surface of the HEMA/MMA copolymer appears to be more orientationally accessible and conformationally active than KGF at the surface of the HEMA/MAA copolymer. They also report that KGF at the surface of the HEMA/MAA copolymer becomes conformationally unfolded, likely due to hydrogen bonding. KGF at the surface of these copolymers can be differentiated by Fourier-transform infrared-attenuated total reflectance spectroscopy and time-of-flight secondary ion mass spectrometry in conjunction with principal component analysis. The differences in KGF orientation and conformation between these copolymers may result in different biological responses in future cell-based experiments.
用于蛋白质递送的水凝胶的开发需要蛋白质与水凝胶之间的相互作用,这种相互作用对蛋白质生物活性的破坏要最小。生物活性会受到诸如受体结合的取向可及性和构象变化等因素的影响,而这些因素又会受到水凝胶表面化学性质的影响。甲基丙烯酸羟乙酯(HEMA)水凝胶作为角质形成细胞生长因子(KGF)的药物递送载体备受关注,已知KGF可促进伤口愈合中的再上皮化。作者在此报告了三种不同的HEMA水凝胶共聚物的表面特性及其对表面结合的KGF的取向和构象的影响。在这项工作中,除了单独的HEMA外,他们还对两种共聚物进行了表征,并报告了蛋白质的取向和构象是如何受到影响的。第一种共聚物包含甲基丙烯酸甲酯(MMA),由于其疏水性,已知它能促进蛋白质吸附到其表面。第二种共聚物包含甲基丙烯酸(MAA),由于其亲水性,已知它能促进蛋白质扩散到其表面。他们发现,与HEMA/MAA共聚物表面的KGF相比,HEMA/MMA共聚物表面的KGF在取向可及性和构象活性方面似乎更高。他们还报告说,HEMA/MAA共聚物表面的KGF可能由于氢键作用而发生构象展开。这些共聚物表面的KGF可以通过傅里叶变换红外衰减全反射光谱和飞行时间二次离子质谱结合主成分分析来区分。这些共聚物之间KGF取向和构象的差异可能会在未来基于细胞的实验中导致不同的生物学反应。