Phase-Separating Peptides Recruiting Aggregation-Induced Emission Fluorogen for Rapid E. coli Detection
Syed Maricar1, Sushanth Gudlur1, Ali Miserez1
1Biological and Biomimetic Material Laboratory (BBML), Center for Sustainable Materials (SusMat), School of Materials Science and Engineering, Nanyang Technological University (NTU), Singapore 637553, Singapore.
Analytical Chemistry
|June 16, 2023
Summary
This study introduces a novel biosensor for rapid E. coli detection using self-assembling peptide condensates and an aggregation-induced emission (AIE)-fluorogen. The assay offers a faster alternative to current methods for identifying bacterial contamination.
Area of Science:
- Biomolecular engineering
- Biosensing technology
- Microbiology
Background:
- Biomolecular condensates are primarily used in drug delivery due to efficient molecular trapping.
- Their application in biosensing remains largely unexplored.
- Rapid and sensitive detection of bacteria like E. coli is crucial for public health.
Purpose of the Study:
- To develop a simple, rapid, and sensitive assay for detecting E. coli.
- To explore the use of phase-separating peptide condensates in biosensing.
- To leverage aggregation-induced emission (AIE) fluorogens for visual detection.
Main Methods:
- Designed phase-separating peptide condensates incorporating an E. coli outer membrane protease (OmpT) recognition site.
- Recruited an AIE-fluorogen into the peptide condensates, which fluoresces upon aggregation.
- Utilized OmpT's enzymatic activity to cleave peptides, disrupting condensate formation and quenching fluorescence.
Main Results:
- Demonstrated successful detection of OmpT activity using recombinant enzyme and subsequently with E. coli K-12.
- Achieved detection of 108 CFU/mL E. coli K-12 within 2 hours in spiked water samples.
- Showed potential for detecting 1-10 CFU/mL with a pre-culture step, significantly faster than commercial kits.
Conclusions:
- The developed assay provides a rapid and visually detectable method for E. coli identification.
- The assay platform is adaptable for detecting other Gram-negative bacteria and diagnostically relevant proteases.
- Further optimization of peptide sequences can enhance detection limits and assay speed.
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