# Real‐Time Tracking of ASCT2‐Mediated Glutamine Uptake in Living Tumors With a Bioorthogonal Bioluminescent Probe

**Authors:** Bing‐Jun Zhou, Ji‐Lei Zhao, Fan Yin, Wen‐Da Chen, Yi Sun, Ying‐Ying Ren, Yi‐Min Chen, Tian Xie, Chong Duan, Jian‐Liang Zhou

PMC · DOI: 10.1002/advs.202507057 · Advanced Science · 2025-08-10

## TL;DR

A new bioluminescent probe tracks glutamine uptake in tumors in real time, offering a better way to study tumor metabolism and develop new treatments.

## Contribution

BLGLN is a novel bioluminescent probe that enables real-time tracking of ASCT2-mediated glutamine uptake in living tumors.

## Key findings

- BLGLN uses Staudinger ligation to monitor glutamine uptake via ASCT2 in living systems.
- The probe simplifies synthesis and eliminates complex sample preparation.
- It allows real-time evaluation of glutamine uptake rates in tumors.

## Abstract

Glutamine addiction, as a hallmark of tumor metabolism, drives malignant progression via proliferation, survival, and metastasis. Alanine‐serine‐cysteine transporter 2 (ASCT2), the primary glutamine transporter, is overexpressed in tumors to meet metabolic demands, making it a promising therapeutic target. Accurately monitoring ASCT2‐mediated glutamine uptake is essential for investigating tumor metabolism and developing ASCT2‐targeted therapeutics. However, current methods lack specificity, require laborious sample processing, and do not support real‐time measurements in living systems. To overcome these issues, BLGLN is designed, an innovative bioluminescent reporter system exploiting Staudinger ligation. BLGLN comprises two components: 1) BL568, a caged D‐luciferin derivative protected with 2‐diphenylphosphinobenzoic acid, and 2) AA201, an azide‐modified glutamine mimetic taken up by ASCT2. Once inside, AA201 undergoes Staudinger ligation with membrane‐permeable BL568, releasing D‐luciferin that is converted by luciferase into a bioluminescent signal, allowing real‐time tracking of ASCT2‐dependent glutamine uptake in tumors. BLGLN provides simplified synthesis, eliminates complex sample preparation, and enables real‐time tracking and evaluation of glutamine uptake rate in living tumors.

A bioluminescent probe, BLGLN, comprising BL568 and ASCT2‐uptaken AA201, enables real‐time monitoring and evaluation of ASCT2‐mediated glutamine uptake rates in living tumors via Staudinger ligation, aiding tumor metabolism studies and targeted therapeutics.

## Linked entities

- **Genes:** SLC1A5 (solute carrier family 1 member 5) [NCBI Gene 6510]
- **Chemicals:** D-luciferin (PubChem CID 92934), 2-diphenylphosphinobenzoic acid (PubChem CID 87021)
- **Diseases:** tumor (MONDO:0005070)

## Full-text entities

- **Genes:** SLC1A5 (solute carrier family 1 member 5) [NCBI Gene 6510] {aka AAAT, ASCT2, ATBO, M7V1, M7VS1, R16}
- **Diseases:** metastasis (MESH:D009362), Tumors (MESH:D009369)
- **Chemicals:** D-luciferin (MESH:C532924), Glutamine (MESH:D005973), 2-diphenylphosphinobenzoic acid (-), azide (MESH:D001386)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12561342/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12561342/full.md

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Source: https://tomesphere.com/paper/PMC12561342