Koch Claudia, Eber Fabian J, Azucena Carlos, Förste Alexander, Walheim Stefan, Schimmel Thomas, Bittner Alexander M, Jeske Holger, Gliemann Hartmut, Eiben Sabine, Geiger Fania C, Wege Christina
Institute of Biomaterials and Biomolecular Systems, Department of Molecular Biology and Plant Virology, University of Stuttgart, Pfaffenwaldring 57, Stuttgart, D-70550, Germany.
Institute of Functional Interfaces (IFG), Chemistry of Oxidic and Organic Interfaces, Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, Eggenstein-Leopoldshafen, Karlsruhe, D-76344, Germany.
Beilstein J Nanotechnol. 2016 Apr 25;7:613-29. doi: 10.3762/bjnano.7.54. eCollection 2016.
The rod-shaped nanoparticles of the widespread plant pathogen tobacco mosaic virus (TMV) have been a matter of intense debates and cutting-edge research for more than a hundred years. During the late 19th century, their behavior in filtration tests applied to the agent causing the 'plant mosaic disease' eventually led to the discrimination of viruses from bacteria. Thereafter, they promoted the development of biophysical cornerstone techniques such as electron microscopy and ultracentrifugation. Since the 1950s, the robust, helically arranged nucleoprotein complexes consisting of a single RNA and more than 2100 identical coat protein subunits have enabled molecular studies which have pioneered the understanding of viral replication and self-assembly, and elucidated major aspects of virus-host interplay, which can lead to agronomically relevant diseases. However, during the last decades, TMV has acquired a new reputation as a well-defined high-yield nanotemplate with multivalent protein surfaces, allowing for an ordered high-density presentation of multiple active molecules or synthetic compounds. Amino acid side chains exposed on the viral coat may be tailored genetically or biochemically to meet the demands for selective conjugation reactions, or to directly engineer novel functionality on TMV-derived nanosticks. The natural TMV size (length: 300 nm) in combination with functional ligands such as peptides, enzymes, dyes, drugs or inorganic materials is advantageous for applications ranging from biomedical imaging and therapy approaches over surface enlargement of battery electrodes to the immobilization of enzymes. TMV building blocks are also amenable to external control of in vitro assembly and re-organization into technically expedient new shapes or arrays, which bears a unique potential for the development of 'smart' functional 3D structures. Among those, materials designed for enzyme-based biodetection layouts, which are routinely applied, e.g., for monitoring blood sugar concentrations, might profit particularly from the presence of TMV rods: Their surfaces were recently shown to stabilize enzymatic activities upon repeated consecutive uses and over several weeks. This review gives the reader a ride through strikingly diverse achievements obtained with TMV-based particles, compares them to the progress with related viruses, and focuses on latest results revealing special advantages for enzyme-based biosensing formats, which might be of high interest for diagnostics employing 'systems-on-a-chip'.
广泛存在的植物病原体烟草花叶病毒(TMV)的杆状纳米颗粒在一百多年来一直是激烈辩论和前沿研究的主题。在19世纪后期,它们在应用于引发“植物花叶病”病原体的过滤试验中的行为最终导致了病毒与细菌的区分。此后,它们推动了电子显微镜和超速离心等生物物理基础技术的发展。自20世纪50年代以来,由单一RNA和2100多个相同外壳蛋白亚基组成的坚固的螺旋排列核蛋白复合物使分子研究得以开展,这些研究开创了对病毒复制和自组装的理解,并阐明了病毒与宿主相互作用的主要方面,而这种相互作用可能导致与农业相关的疾病。然而,在过去几十年中,TMV作为一种具有明确多价蛋白质表面的高产纳米模板获得了新的声誉,它能够有序地高密度呈现多种活性分子或合成化合物。暴露在病毒衣壳上的氨基酸侧链可以通过基因或生化方法进行调整,以满足选择性共轭反应的需求,或直接在TMV衍生的纳米棒上设计新的功能。天然TMV的尺寸(长度:300纳米)与肽、酶、染料、药物或无机材料等功能配体相结合,有利于从生物医学成像和治疗方法到电池电极表面扩大再到酶固定化等广泛的应用。TMV构建块也适合体外组装的外部控制以及重组为技术上方便的新形状或阵列,这为“智能”功能3D结构的开发具有独特的潜力。其中,为基于酶的生物检测布局设计的材料,例如常规用于监测血糖浓度的材料,可能会特别受益于TMV棒的存在:最近的研究表明,它们的表面在连续重复使用数周后能稳定酶活性。这篇综述带领读者领略了基于TMV的颗粒所取得的惊人多样的成果,将它们与相关病毒的进展进行了比较,并重点关注了揭示基于酶的生物传感形式特殊优势的最新结果,这对于采用“芯片上的系统”进行诊断可能具有很高的兴趣。