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Updated: Nov 27, 2025

Detecting and Characterizing Protein Self-Assembly In Vivo by Flow Cytometry
Published on: July 17, 2019
Self-Reporting of Folding and Aggregation by Orthogonal Hantzsch Luminophores Within a Single Polymer Chain
Julen De-La-Cuesta1, Ester Verde-Sesto1, Arantxa Arbe1
1Centro de Física de Materiales (CSIC-UPV/EHU)-Materials Physics Center MPC, P° Manuel de Lardizabal 5, 20018, Donostia, Spain.
Abstract:
Self-reporting fluorescence methods for monitoring folding and aggregation of proteins have a long history in biochemistry. Placing orthogonal luminophores within individual synthetic polymer chains for self-reporting both folding (i.e., its intramolecular compaction to isolated single-chain nanoparticles, SCNPs) and unbidden aggregation (i.e., the intermolecular association of SCNPs) remains a great challenge. Herein, a simple and efficient platform to identify both single-chain compaction and intermolecular aggregation phenomena via photoluminescence is presented based on simultaneous synthesis through Hantzsch ester formation of orthogonal luminophores within the same polymer chain. Starting from non-luminescent β-ketoester-decorated chains, intramolecular compaction is visually detected through fluorescence arising from Hantzsch fluorophores generated as intra-chain connectors during folding. Complementary, intermolecular association is identified via aggregation-induced emission (AIE) from orthogonal luminophores displaying intense photoluminescence at redshifted wavelengths after formation of multi-SCNPs assemblies.
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