Bioorganic Methodology to Create Novel Biomolecular Platforms to Address Critical Needs in Molecular Recognition and Function

该研究计划的重点是创造新型生物分子支架，这些支架将成为小有机和无机分子的选择性亲和受体的化学设计的关键要素，以及用于控制与化学表面和先进材料的大分子相互作用的独特分子框架。创新分子识别系统的创建是一项关键的使能技术，它支持为社会开发新材料和治疗剂。复杂的多亚基蛋白质和病毒的化学和生物化学操作将作为独特的，自组装的生物分子平台，对材料和生物材料科学有价值。目前，人们对大的多亚基蛋白质和病毒的应用产生了浓厚的兴趣，这些蛋白质和病毒可以用于合成能够“悬挂和定向”光伏系统的分子支架，或者用作制造生物分子电池、新型生物纤维或药物递送系统的构建块。因此，非常需要开发这些复杂结构的化学，并培养下一代科学家，为可再生生物系统在材料科学，能源系统和治疗学中的应用做出贡献。将通过这些化学方法探索生物分子复杂性的各种水平。这些包括：*A）含空腔的多亚基球形蛋白的化学操作和蛋白质工程化，所述球形蛋白的复杂性（24至180个蛋白质亚基）、质量（440 kDa至6.9 MDa）和直径（120-320）的范围。我们在这一领域的研究计划是开发新的方法来控制其内部和外部分子表面，以及开发方法来创建新的主客体大分子复合物使用工程蛋白质成分。B）开发生物有机方法以产生新型“基于病毒的分子平台”（线性噬菌体M13，~ 2770个蛋白质亚基，直径~ 60，长度~ 1微米;质量16.8 MDa），以用作在材料和（生物）材料科学中潜在有用的独特生物分子支架。我们已经成功地利用生物有机方法将非天然氨基酸掺入M13的主要鞘蛋白中，并且在一个实施例中，在M13表面上展示了> 350个叠氮化物部分，其被进一步化学修饰以可控地附着荧光染料和金纳米颗粒。探索这种工程噬菌体的额外能力的研究将继续进行。例如，将识别肽放置在这些噬菌体支架的“末端”上并进一步将它们交联成更大的复合物的能力，应该允许将这些大复合物分子递送和/或靶向到各种材料和表面。

This research program focuses on the creation of novel biomolecular scaffolds that will become key elements in the chemical design of selective affinity receptors for small organic and inorganic molecules as well as unique molecular frameworks useful in controlling macromolecule interactions with chemical surfaces and advanced materials. The creation of innovative molecular recognition systems is a critical enabling technology that underpins the development of new materials and therapeutic agents for society. Chemical and biochemical manipulation of complex multisubunit proteins and viruses will be undertaken to serve as unique, self-assembling biomolecular platforms valuable for materials and biomaterials science. Currently intense interest is being directed toward the application of large multisubunit proteins and viruses to the synthesis of molecular scaffolds able to "hang and orient" photovoltaic systems, or to serve as building blocks for the fabrication of biomolecular batteries, novel biofibers or drug delivery systems. Hence there is exceptional need for developing the chemistry of these complex structures and to train the next generation of scientists to contribute to the application of renewable biosystems to materials science, energy systems and therapeutics. Various levels of biomolecular complexity will be explored by these chemical approaches. These include:***A) Chemical manipulation and protein engineering of cavity-containing multisubunit spherical proteins which range in complexity (24 to 180 protein subunits), mass (440 kDa to 6.9 MDa) and diameter (120-320 ). Our research program in this area is to develop new ways to control their inner and outer molecular surfaces as well as to develop approaches to create new host-guest macromolecular complexes using engineered protein components.***B) Development of bioorganic approaches to create novel "virus-based molecular platforms" (linear bacteriophage M13, ~ 2770 protein subunits, ~ 60 in diameter and ~ 1 micron in length; mass 16.8 MDa) to serve as unique biomolecular scaffolds potentially useful in materials and (bio)materials science. We have successfully utilized a bioorganic approach to incorporate unnatural amino acids into the major sheath protein of M13 and, in one example, displayed > 350 azide moieties on the M13 surface which were further chemically modified to controllably attach fluorescent dyes and gold nanoparticles. Research to explore the additional capabilities of this engineered bacteriophage will be continued. For example, the ability to place recognition peptides onto the “ends” of these bacteriophage scaffolds and to furthermore crosslink them into larger complexes, should allow for the molecular delivery and/or targeting of these megabiocomplexes to a variety of materials and surfaces.**