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A Two-Photon Excitation Based Fluorogenic Probe for Sialome Imaging in Living Systems
Lei Rong1, Chi Zhang2, Qi Lei2
1Key Laboratory of Biomedical Polymers of Ministry of Education and Department of Chemistry Wuhan University Wuhan 430072 P.R. China; State Key Laboratory of Virology College of Life Sciences Wuhan University Wuhan 430072 P.R. China.
A novel fluorogenic probe, Naph-yne, utilizes alkyne-modified naphthalimide fluorescence for imaging azide-tagged mannosyl glycoproteins. This advanced imaging technique is effective in both cellular studies and vertebrate model organisms.
Area of Science:
- Biochemistry
- Chemical Biology
- Molecular Imaging
Background:
- Glycoproteins play crucial roles in various biological processes.
- Accurate imaging of glycoproteins is essential for understanding cellular functions and disease mechanisms.
- Current imaging methods may have limitations in sensitivity or specificity.
Purpose of the Study:
- To develop a novel two-photon excited fluorogenic probe for sensitive and specific imaging of azide-tagged mannosyl glycoproteins.
- To demonstrate the utility of the probe in both cellular imaging and in vivo studies using vertebrate model organisms.
Main Methods:
- Synthesis of an alkyne-modified naphthalimide derivative as a fluorogenic probe (Naph-yne).
- Utilizing the fluorescence property of the probe for two-photon excitation.
- Application of the probe for imaging azide-tagged mannosyl glycoproteins in cellular and organismal models.
Main Results:
- The Naph-yne probe exhibits strong fluorescence upon reaction with azide-tagged targets.
- Successful imaging of mannosyl glycoproteins at the cellular level was achieved.
- The probe demonstrated efficacy in imaging mannosyl glycoproteins within vertebrate model organisms.
Conclusions:
- Naph-yne is a highly effective two-photon excited fluorogenic probe for visualizing azide-tagged mannosyl glycoproteins.
- The probe offers a valuable tool for advanced biological imaging in diverse model systems.
- This work advances the field of molecular imaging for glycoprotein studies.
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