Division of Biology, Beckman Institute, California Institute of Technology, Pasadena, California, USA.
Nat Protoc. 2012 Sep;7(9):1618-33. doi: 10.1038/nprot.2012.087. Epub 2012 Aug 9.
To address the need for a bright, photostable labeling tool that allows long-term in vivo imaging in whole organisms, we recently introduced second harmonic generating (SHG) nanoprobes. Here we present a protocol for the preparation and use of a particular SHG nanoprobe label, barium titanate (BT), for in vivo imaging in living zebrafish embryos. Chemical treatment of the BT nanoparticles results in surface coating with amine-terminal groups, which act as a platform for a variety of chemical modifications for biological applications. Here we describe cross-linking of BT to a biotin-linked moiety using click chemistry methods and coating of BT with nonreactive poly(ethylene glycol) (PEG). We also provide details for injecting PEG-coated SHG nanoprobes into zygote-stage zebrafish embryos, and in vivo imaging of SHG nanoprobes during gastrulation and segmentation. Implementing the PROCEDURE requires a basic understanding of laser-scanning microscopy, experience with handling zebrafish embryos and chemistry laboratory experience. Functionalization of the SHG nanoprobes takes ∼3 d, whereas zebrafish preparation, injection and imaging setup should take approximately 2-4 h.
为满足在整个生物体中进行长期体内成像的需要,我们最近引入了二次谐波产生(SHG)纳米探针。本文提供了一种使用特定 SHG 纳米探针标记物钛酸钡(BT)的方案,用于活体斑马鱼胚胎的体内成像。BT 纳米颗粒的化学处理导致表面涂覆有胺端基,可作为用于各种生物应用的化学修饰的平台。这里我们描述了使用点击化学方法将 BT 交联到生物素连接部分,并将 BT 涂覆有非反应性聚乙二醇(PEG)。我们还提供了将 PEG 涂覆的 SHG 纳米探针注入合子期斑马鱼胚胎中以及在原肠胚形成和体节形成期间进行 SHG 纳米探针体内成像的详细信息。实施该方案需要对激光扫描显微镜有基本的了解,对斑马鱼胚胎的处理和化学实验室经验有一定的经验。SHG 纳米探针的功能化大约需要 3 天,而斑马鱼的准备、注射和成像设置大约需要 2-4 小时。