Fluorogenic Ag+–Tetrazolate Aggregation Enables Efficient Fluorescent Biological Silver Staining

Silver staining, which exploits the special bioaffinity and the chromogenic reduction of silver ions, is an indispensable visualization method in biology. It is a most popular method for in‐gel protein detection. However, it is limited by run‐to‐run variability, background staining, inability for pr...

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Published inAngewandte Chemie Vol. 130; no. 20; pp. 5852 - 5855
Main Authors Xie, Sheng, Wong, Alex Y. H., Kwok, Ryan T. K., Li, Ying, Su, Huifang, Lam, Jacky W. Y., Chen, Sijie, Tang, Ben Zhong
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 14.05.2018
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Summary:Silver staining, which exploits the special bioaffinity and the chromogenic reduction of silver ions, is an indispensable visualization method in biology. It is a most popular method for in‐gel protein detection. However, it is limited by run‐to‐run variability, background staining, inability for protein quantification, and limited compatibility with mass spectroscopic (MS) analysis; limitations that are largely attributed to the tricky chromogenic visualization. Herein, we reported a novel water‐soluble fluorogenic Ag+ probe, the sensing mechanism of which is based on an aggregation‐induced emission (AIE) process driven by tetrazolate‐Ag+ interactions. The fluorogenic sensing can substitute the chromogenic reaction, leading to a new fluorescence silver staining method. This new staining method offers sensitive detection of total proteins in polyacrylamide gels with a broad linear dynamic range and robust operations that rival the silver nitrate stain and the best fluorescent stains. Fluorogenes Silber: Ein fluorogener Ag+‐Nachweis beruht auf spontaner Tetrazolat‐Ag+‐Aggregation. Dieses System umgeht den kniffligen chromogenen Reduktionsschritt bei herkömmlichen Silberanfärbungsmethoden durch einen fluorogenen Nachweisschritt. Das Resultat ist eine empfindliche und robuste Fluoreszenzvisualisierung ganzer Proteine.
ISSN:0044-8249
1521-3757
DOI:10.1002/ange.201801653