Bioorthogonal Heptose Phosphate Probes for Chemical Profiling of Bacterial Glycans

High Resolution Image Download MS PowerPoint Slide Heptose sugars are essential components of Gram-negative bacterial lipopolysaccharide (LPS) and play emerging roles in innate immune activation. To enable functional studies of heptose biology, we developed a bioorthogonal metabolic probe, 7-azido-heptose-1-phosphate (7AzHep1P), which incorporates into the LPS inner core and generates a truncated yet detectable LPS structure. Using click chemistry, we visualized LPS remodeling in live bacteria and confirmed reporter incorporation across various LPS mutants. Notably, 7AzHep1P-labeled LPS preserved immunogenic activity, triggering cytokine release and macrophage activation. We further applied this probe for chemical glycoproteomics, identifying 133 O -heptosylated glycopeptides from 97 bacterial proteins. Beyond canonical serine and threonine sites, heptosylation was also detected on other residues, revealing unappreciated substrate diversity. Together, this strategy enables nongenetic, in situ profiling of heptose-linked biomolecules, offering a valuable tool for dissecting LPS biosynthesis, immune modulation, and glycosylation in bacterial systems.

Authors

Institutions

Publication Details

Journal
JACS Au
Published
2026-06-12
DOI
https://doi.org/10.1021/jacsau.6c00391
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Bioorthogonal Heptose Phosphate Probes for Chemical Profiling of Bacterial Glycans

Wei Wang, T L Li, Yi Hsu, Ran Xie et al.
JACS Au
Glycosylation and Glycoproteins Research
article

Bioorthogonal Heptose Phosphate Probes for Chemical Profiling of Bacterial Glycans

Wei Wang, T L Li, Yi Hsu, Ran Xie, Xiaocui Zheng, Ruhong Zhou, Senlian Hong, Wei Cao, Li Li, Li Y, W.T. Liu, Yi-Xiang Wang, Lu Yu, Han Wang, Ming Yang, Yixuan Xie, Jiaming Jin, Chang Xu
article en

Abstract

High Resolution Image Download MS PowerPoint Slide Heptose sugars are essential components of Gram-negative bacterial lipopolysaccharide (LPS) and play emerging roles in innate immune activation. To enable functional studies of heptose biology, we developed a bioorthogonal metabolic probe, 7-azido-heptose-1-phosphate (7AzHep1P), which incorporates into the LPS inner core and generates a truncated yet detectable LPS structure. Using click chemistry, we visualized LPS remodeling in live bacteria and confirmed reporter incorporation across various LPS mutants. Notably, 7AzHep1P-labeled LPS preserved immunogenic activity, triggering cytokine release and macrophage activation. We further applied this probe for chemical glycoproteomics, identifying 133 O -heptosylated glycopeptides from 97 bacterial proteins. Beyond canonical serine and threonine sites, heptosylation was also detected on other residues, revealing unappreciated substrate diversity. Together, this strategy enables nongenetic, in situ profiling of heptose-linked biomolecules, offering a valuable tool for dissecting LPS biosynthesis, immune modulation, and glycosylation in bacterial systems.

JACS Au
Henan University (CN), Biocon (Switzerland) (CH), Fudan University (CN), State Key Laboratory of Chemical Engineering (CN), Nanjing University (CN)
National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, Natural Science Foundation of Jiangsu Province, National Key Research and Development Program of China, Beijing National Laboratory for Molecular Sciences
Openalex Percentile: Top 10%
Glycosylation and Glycoproteins Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.