Center for DNA Nanotechnology at the Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University , Gustav Wieds Vej 14, 8000 Aarhus C, Denmark.
Acc Chem Res. 2017 Jun 20;50(6):1367-1374. doi: 10.1021/acs.accounts.6b00618. Epub 2017 May 9.
Conjugation of DNA to proteins is increasingly used in academia and industry to provide proteins with tags for identification or handles for hybridization to other DNA strands. Assay technologies such as immuno-PCR and proximity ligation and the imaging technology DNA-PAINT require DNA-protein conjugates. In DNA nanotechnology, the DNA handle is exploited to precisely position proteins by self-assembly. For these applications, site-selective conjugation is almost always desired because fully functional proteins are required to maintain the specificity of antibodies and the activity of enzymes. The introduction of a bioorthogonal handle at a specific position of a protein by recombinant techniques provides an excellent approach to site-specific conjugation, but for many laboratories and for applications where several proteins are to be labeled, the expression of recombinant proteins may be cumbersome. In recent years, a number of chemical methods that target conjugation to specific sites at native proteins have become available, and an overview of these methods is provided in this Account. Our laboratory has investigated DNA-templated protein conjugation (DTPC), which offers an alternative approach to site-selective conjugation of DNA to proteins. The method is inspired by the concept of DNA-templated synthesis where functional groups conjugated to DNA strands are preorganized by DNA hybridization to dramatically increase the reaction rate. In DPTC, we target metal binding sites in proteins to template selective covalent conjugation reactions. By chelation of a DNA-metal complex with a metal binding site of the protein, an electrophile on a second DNA strand is aligned for reaction with a lysine side chain on the protein in the proximity of the metal binding site. The method is quite general because approximately one-third of all wild-type proteins contain metal-binding sites, including many IgG antibodies, and it is also applicable to His-tagged proteins. This emerging field provides direct access to site-selective conjugates of DNA to commercially available proteins. In this Account, we introduce these methods to the reader and describe current developments and future aspects.
DNA 与蛋白质的连接在学术界和工业界中越来越多地被用于为蛋白质提供标记物以进行鉴定或用于与其他 DNA 链杂交。免疫-PCR 和邻近连接等分析技术以及 DNA-PAINT 成像技术都需要 DNA-蛋白质偶联物。在 DNA 纳米技术中,通过自组装利用 DNA 手柄精确定位蛋白质。对于这些应用,几乎总是需要位点选择性偶联,因为需要完全功能的蛋白质来保持抗体的特异性和酶的活性。通过重组技术在蛋白质的特定位置引入生物正交手柄为位点特异性偶联提供了一种极好的方法,但是对于许多实验室和需要标记多个蛋白质的应用,表达重组蛋白质可能很麻烦。近年来,出现了许多针对天然蛋白质中特定位置偶联的化学方法,本文对这些方法进行了概述。我们实验室研究了 DNA 模板化蛋白质偶联(DTPC),这为 DNA 与蛋白质的位点选择性偶联提供了一种替代方法。该方法的灵感来自于 DNA 模板化合成的概念,其中连接到 DNA 链的官能团通过 DNA 杂交预先组织,从而极大地提高了反应速率。在 DTPC 中,我们针对蛋白质中的金属结合位点来模板选择性的共价偶联反应。通过 DNA-金属配合物与蛋白质中金属结合位点的螯合,将第二 DNA 链上的亲电试剂与靠近金属结合位点的蛋白质上的赖氨酸侧链对齐以进行反应。该方法非常通用,因为大约三分之一的野生型蛋白质都包含金属结合位点,包括许多 IgG 抗体,并且也适用于 His 标记的蛋白质。这个新兴领域为商业上可获得的蛋白质提供了直接进行 DNA 位点选择性偶联的方法。在本说明中,我们向读者介绍这些方法,并描述当前的发展和未来的方向。