Department of Chemistry and Biochemistry, University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, IN, 46556, USA.
Angew Chem Int Ed Engl. 2020 Dec 21;59(52):23740-23747. doi: 10.1002/anie.202009599. Epub 2020 Oct 29.
A general synthetic method creates a new class of covalently connected, self-threaded, fluorescent molecular probes with figure-eight topology, an encapsulated deep-red fluorophore, and two peripheral peptide loops. The globular molecular shape and rigidified peptide loops enhance imaging performance by promoting water solubility, eliminating probe self-aggregation, and increasing probe stability. Moreover, the peptide loops determine the affinity and selectivity for targets within complex biological samples such as cell culture, tissue histology slices, or living subjects. For example, a probe with cell-penetrating peptide loops targets the surface of cell plasma membranes, whereas, a probe with bone-targeting peptide loops selectively stains the skeleton within a living mouse. The unique combination of bright deep-red fluorescence, high stability, and predictable peptide-based targeting is ideal for photon intense fluorescence microscopy and biological imaging.
一种通用的合成方法创建了一类新的共价连接的、自缠绕的、具有 8 字形拓扑结构的荧光分子探针,它包含一个封装的深红色荧光团和两个外围肽环。球形分子形状和刚性肽环通过提高水溶性、消除探针自聚集和增加探针稳定性来增强成像性能。此外,肽环决定了在细胞培养、组织组织学切片或活体等复杂生物样本中对目标的亲和力和选择性。例如,带有穿透肽环的探针靶向细胞质膜的表面,而带有骨靶向肽环的探针则选择性地染色活体小鼠内的骨骼。强亮深红色荧光、高稳定性和可预测的肽基靶向的独特组合非常适合光子强荧光显微镜和生物成像。