Department of Chemistry, University of California, Berkeley, California 94720, United States.
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratories, Berkeley, California 94720, United States.
J Am Chem Soc. 2021 May 19;143(19):7342-7350. doi: 10.1021/jacs.0c11678. Epub 2021 May 3.
A new enzymatic method is reported for constructing protein- and DNA-AuNP conjugates. The strategy relies on the initial functionalization of AuNPs with phenols, followed by activation with the enzyme tyrosinase. Using an oxidative coupling reaction, the activated phenols are coupled to proteins bearing proline, thiol, or aniline functional groups. Activated phenol-AuNPs are also conjugated to a small molecule biotin and commercially available thiol-DNA. Advantages of this approach for AuNP bioconjugation include: (1) initial formation of highly stable AuNPs that can be selectively activated with an enzyme, (2) the ability to conjugate either proteins or DNA through a diverse set of functional handles, (3) site-specific immobilization, and (4) facile conjugation that is complete within 2 h at room temperature under aqueous conditions. The enzymatic oxidative coupling on AuNPs is applied to the construction of tobacco mosaic virus (TMV)-AuNP conjugates, and energy transfer between the AuNPs and fluorophores on TMV is demonstrated.
一种新的酶法被用于构建蛋白质和 DNA-金纳米颗粒(AuNP)缀合物。该策略依赖于 AuNP 与酚的初始功能化,然后用酶酪氨酸酶进行激活。通过氧化偶联反应,激活的酚与带有脯氨酸、巯基或苯胺官能团的蛋白质偶联。激活的酚-AuNP 也与小分子生物素和市售的巯基 DNA 偶联。该方法用于 AuNP 生物缀合的优点包括:(1)初始形成高度稳定的 AuNP,可以用酶选择性激活;(2)能够通过多种功能接头偶联蛋白质或 DNA;(3)定点固定;(4)在室温下在水性条件下 2 小时内即可完成的简便缀合。AuNP 上的酶促氧化偶联被应用于构建烟草花叶病毒(TMV)-AuNP 缀合物,并证明了 AuNP 与 TMV 上荧光团之间的能量转移。