Evidence map›Paper›PMID 39167637›Full record

ArticleScience advances2024

Click-free imaging of carbohydrate trafficking in live cells using an azido photothermal probe.

Qing Xia, Harini A Perera, Rylie Bolarinho, Zeke A Piskulich, Zhongyue Guo, Jiaze Yin, Hongjian He, Mingsheng Li, Xiaowei Ge, Qiang Cui and 3 more

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Qing XiaDepartment of Electrical and Computer Engineering, Boston University, Boston, MA 02215, USA.ORCID 0000-0002-5939-2972
Harini A PereraDepartment of Chemistry, University of Massachusetts, Lowell, MA 01854, USA.ORCID 0000-0002-9514-6170
Rylie BolarinhoDepartment of Chemistry, Boston University, Boston, MA 02215, USA.ORCID 0000-0002-8620-3583
Zeke A PiskulichDepartment of Chemistry, Boston University, Boston, MA 02215, USA.ORCID 0000-0003-0304-305X
Zhongyue GuoDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Jiaze YinDepartment of Electrical and Computer Engineering, Boston University, Boston, MA 02215, USA.ORCID 0000-0001-6080-3073
Hongjian HeDepartment of Electrical and Computer Engineering, Boston University, Boston, MA 02215, USA.
Mingsheng LiDepartment of Electrical and Computer Engineering, Boston University, Boston, MA 02215, USA.
Xiaowei GeDepartment of Electrical and Computer Engineering, Boston University, Boston, MA 02215, USA.ORCID 0000-0001-8938-9304
Qiang CuiDepartment of Chemistry, Boston University, Boston, MA 02215, USA.ORCID 0000-0001-6214-5211
Olof RamströmDepartment of Chemistry, University of Massachusetts, Lowell, MA 01854, USA.ORCID 0000-0002-1533-6514
Mingdi YanDepartment of Chemistry, University of Massachusetts, Lowell, MA 01854, USA.ORCID 0000-0003-1121-4007
Ji-Xin ChengDepartment of Electrical and Computer Engineering, Boston University, Boston, MA 02215, USA.ORCID 0000-0002-5607-6683

Funding

Vibrational Spectroscopic Imaging to Unveil Hidden Signatures in Living SystemsR35GM136223 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI CHENG, JI-XIN · 2020 to 2025
$5.7M
Rapid AST through Metabolic Imaging at Single Cell LevelR01AI141439 · NIAID · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI Ji-Xin Cheng · 2019 to 2026
$4.7M
Mapping Cancer Metabolism by Mid-infrared Photothermal MicroscopyR33CA261726 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI CHENG, JI-XIN · 2021 to 2023
$1.2M
NCI NIH HHS R33 CA261726NIAID NIH HHS R01 AI141439NIGMS NIH HHS R35 GM136223
6 · The paper itself

Abstract

Real-time tracking of intracellular carbohydrates remains challenging. While click chemistry allows bio-orthogonal tagging with fluorescent probes, the reaction permanently alters the target molecule and only allows a single snapshot. Here, we demonstrate click-free mid-infrared photothermal (MIP) imaging of azide-tagged carbohydrates in live cells. Leveraging the micromolar detection sensitivity for 6-azido-trehalose (TreAz) and the 300-nm spatial resolution of MIP imaging, the trehalose recycling pathway in single mycobacteria, from cytoplasmic uptake to membrane localization, is directly visualized. A peak shift of azide in MIP spectrum further uncovers interactions between TreAz and intracellular protein. MIP mapping of unreacted azide after click reaction reveals click chemistry heterogeneity within a bacterium. Broader applications of azido photothermal probes to visualize the initial steps of the Leloir pathway in yeasts and the newly synthesized glycans in mammalian cells are demonstrated.

Indexed as

AzidesClick ChemistryBiological TransportCarbohydratesFluorescent DyesHumansTrehaloseAzidesCarbohydratesFluorescent DyesTrehalose

Identifiers

PMID39167637
PMCPMC11338237

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.