Institute for Frontier Materials, Deakin University , Geelong, Victoria 3216, Australia.
Department of Chemistry, University of Miami , 1301 Memorial Drive, Coral Gables, Florida 33146, United States.
Chem Rev. 2017 Oct 25;117(20):12641-12704. doi: 10.1021/acs.chemrev.7b00139. Epub 2017 Aug 29.
Peptide sequences are known to recognize and bind different nanomaterial surfaces, which has resulted in the screening and identification of hundreds of peptides with the ability to bind to a wide range of metallic, metal oxide, mineral, and polymer substrates. These biomolecules are able to bind to materials with relatively high affinity, resulting in the generation of a complex biointerface between the biotic and abiotic components. While the number of material-binding sequences is large, at present, quantitative materials-binding characterization of these peptides has been accomplished only for a relatively small number of sequences. Moreover, it is currently very challenging to determine the molecular-level structure(s) of these peptides in the materials adsorbed state. Despite this lack of data related to the structure and function of this remarkable biointerface, several of these peptide sequences have found extensive use in creating functional nanostructured materials for assembly, catalysis, energy, and medicine, all of which are dependent on the structure of the individual peptides and collective biointerface at the material surface. In this Review, we provide a comprehensive overview of these applications and illustrate how the versatility of this peptide-mediated approach for the growth, organization, and activation of nanomaterials could be more widely expanded via the elucidation of biointerfacial structure/property relationships. Future directions and grand challenges to realize these goals are highlighted for both experimental characterization and molecular-simulation strategies.
肽序列已知可识别和结合不同的纳米材料表面,这导致了数百种能够结合广泛的金属、金属氧化物、矿物和聚合物基底的肽的筛选和鉴定。这些生物分子能够与材料以相对较高的亲和力结合,从而在生物和非生物成分之间产生复杂的生物界面。虽然具有材料结合序列的数量很大,但目前,这些肽的定量材料结合特性仅在相对较少的序列上得到了描述。此外,目前确定这些吸附在材料上的肽的分子水平结构非常具有挑战性。尽管与这个显著的生物界面的结构和功能相关的数据很少,但这些肽序列中的几个已被广泛用于制造用于组装、催化、能源和医学的功能性纳米结构材料,所有这些都依赖于单个肽的结构和集体生物界面在材料表面上。在这篇综述中,我们全面概述了这些应用,并说明了通过阐明生物界面的结构/性能关系,如何通过肽介导的方法更广泛地扩展这种方法在纳米材料的生长、组织和激活方面的多功能性。突出了为实现这些目标的实验表征和分子模拟策略的未来方向和重大挑战。