Tamerler Candan, Sarikaya Mehmet
Materials Science and Engineering, University of Washington, Seattle, WA 98195, USA.
Acta Biomater. 2007 May;3(3):289-99. doi: 10.1016/j.actbio.2006.10.009. Epub 2007 Jan 25.
In nature, proteins are the machinery that accomplish many functions through their specific recognition and interactions in biological systems from single-celled to multicellular organisms. Biomolecule-material interaction is accomplished via molecular specificity, leading to the formation of controlled structures and functions at all scales of dimensional hierarchy. Through evolution, molecular recognition and, consequently, functions developed through successive cycles of mutation and selection. Using biology as a guide, we can now understand, engineer and control peptide-material interactions and exploit these to tailor novel materials and systems for practical applications. We adapted combinatorial biology protocols to display peptide libraries, either on the cell surface or on phages, to select short peptides specific to a variety of practical materials systems. Following the selection step, we determined the kinetics and stability of peptide binding experimentally to understand the bound peptide structure via modeling and its assembly via atomic force microscopy. The peptides were further engineered to have multiple repeats or their amino acid sequences varied to tailor their function. Both nanoparticles and flat inorganic substrates containing multimaterials patterned at the nano- and microscales were used for self-directed immobilization of molecular constructs. The molecular biomimetic approach opens up new avenues for the design and utilization of multifunctional molecular systems with wide ranging applications, from tissue engineering, drug delivery and biosensors, to nanotechnology and bioremediation. Here we give examples of protein-mediated functional materials in biology, peptide selection and engineering with affinity to inorganics, demonstrate potential utilizations in materials science, engineering and medicine, and describe future prospects.
在自然界中,蛋白质是一种机制,通过其在从单细胞生物到多细胞生物的生物系统中的特异性识别和相互作用来完成多种功能。生物分子与材料的相互作用是通过分子特异性实现的,这导致在各个维度层次上形成可控的结构和功能。通过进化,分子识别以及由此通过连续的突变和选择循环发展而来的功能得以形成。以生物学为指导,我们现在能够理解、设计和控制肽与材料的相互作用,并利用这些相互作用来定制新型材料和系统以用于实际应用。我们采用组合生物学方案在细胞表面或噬菌体上展示肽库,以筛选出对各种实际材料系统具有特异性的短肽。在筛选步骤之后,我们通过实验确定肽结合的动力学和稳定性,以通过建模了解结合肽的结构,并通过原子力显微镜了解其组装情况。对肽进行进一步改造,使其具有多个重复序列或改变其氨基酸序列以调整其功能。含有在纳米和微米尺度上图案化的多种材料的纳米颗粒和平板无机底物都用于分子构建体的自定向固定。分子仿生方法为多功能分子系统的设计和利用开辟了新途径,其应用范围广泛,从组织工程、药物递送和生物传感器到纳米技术和生物修复。在此,我们给出生物学中蛋白质介导的功能材料的实例、对无机物具有亲和力的肽的筛选和工程设计,展示其在材料科学、工程和医学中的潜在应用,并描述未来前景。