| Literature DB >> 28898567 |
Xiaofeng Fang1,2, Xuanze Chen3, Rongqin Li3, Zhihe Liu2, Haobin Chen2, Zezhou Sun2, Bo Ju4, Yifei Liu4, Sean Xiao-An Zhang4, Dan Ding5, Yujie Sun3, Changfeng Wu1.
Abstract
Aggregation induced emission (AIE) has attracted considerable interest for the development of fluorescence probes. However, controlling the bioconjugation and cellular labeling of AIE dots is a challenging problem. Here, this study reports a general approach for preparing small and bioconjugated AIE dots for specific labeling of cellular targets. The strategy is based on the synthesis of oxetane-substituted AIEgens to generate compact and ultrastable AIE dots via photo-crosslinking. A small amount of polymer enriched with oxetane groups is cocondensed with most of the AIEgens to functionalize the nanodot surface for subsequent streptavidin bioconjugation. Due to their small sizes, good stability, and surface functionalization, the cell-surface markers and subcellular structures are specifically labeled by the AIE dot bioconjugates. Remarkably, stimulated emission depletion imaging with AIE dots is achieved for the first time, and the spatial resolution is significantly enhanced to ≈95 nm. This study provides a general approach for small functional molecules for preparing small sized and ultrastable nanodots.Entities:
Keywords: aggregation-induced emission; nanodots; photo-crosslinking; specific labeling; subcellular structures; super-resolution imaging
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Year: 2017 PMID: 28898567 DOI: 10.1002/smll.201702128
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281