Institute of Biochemistry, Biocenter; Cluster of Excellence Frankfurt, Goethe-University Frankfurt, Max-von-Laue-Str. 9, 60438 Frankfurt/M. (Germany) http://www.biochem.uni-frankfurt.de http://www.smb.uni-frankfurt.de.
Institute of Physical and Theoretical Chemistry, Goethe-University Frankfurt, Max-von-Laue-Str. 7, 60438 Frankfurt/M. (Germany).
Angew Chem Int Ed Engl. 2015 Aug 24;54(35):10216-9. doi: 10.1002/anie.201503215. Epub 2015 Jul 15.
Protein labeling with synthetic fluorescent probes is a key technology in chemical biology and biomedical research. A sensitive and efficient modular labeling approach (SLAP) was developed on the basis of a synthetic small-molecule recognition unit (Ni-trisNTA) and the genetically encoded minimal protein His6-10 -tag. High-density protein tracing by SLAP was demonstrated. This technique allows super-resolution fluorescence imaging and fulfills the necessary sampling criteria for single-molecule localization-based imaging techniques. It avoids masking by large probes, for example, antibodies, and supplies sensitive, precise, and robust size analysis of protein clusters (nanodomains).
蛋白质的合成荧光探针标记是化学生物学和生物医学研究的关键技术。在合成小分子识别单元(Ni-trisNTA)和遗传编码的最小蛋白 His6-10 标签的基础上,开发了一种灵敏、高效的模块化标记方法(SLAP)。通过 SLAP 进行高密度蛋白质示踪得到了验证。该技术允许进行超分辨率荧光成像,并满足基于单分子定位的成像技术的必要采样标准。它避免了大探针(例如抗体)的掩蔽,并提供了对蛋白质簇(纳米域)的灵敏、精确和稳健的尺寸分析。