Ge Lab · Shenzhen Bay Laboratory

Reading the language of glycans, from single sites to entire condensates.

We follow a read–edit–engineer framework along the protein- and RNA-glycan axes — building precise glycan-editing tools, decoding glycan function in biomolecular condensates and cellular processes, and converting that knowledge into therapeutic strategies such as tumour immunotherapy.

23
Publications since 2012
13
Group members
5
Collaborating institutions
3
Research directions
Research directions

One framework, three threads

The glycome underpins molecular interaction and information flow in living systems. Along the protein- and RNA-glycan axes, we ask three questions in sequence: can we edit glycans precisely? how do their functions unfold? and can we convert that knowledge into diagnostics and therapeutics?

All research →
A schematic of the "read–edit–engineer" framework for glycan chemical biology, spanning the protein-glycan and RNA-glycan axes.

Precise Glycan Editing

We develop spatiotemporally resolved, substrate-selective editing tools and interface-level interventions along both protein-glycan and RNA-glycan axes to enable precise glycan control in defined biological contexts.

Editing toolsProtein glycansRNA glycans

Functional Decoding

Using interdisciplinary chemical-biology tools, we dissect functional interactions between glycans and proteins/RNA in defined spatial and state contexts — from biomolecular condensates to the plasma membrane — and study how glycans shape transcription, translation, and other fundamental cellular processes.

CondensatesTranscriptionTranslation

Translational Applications

We map functional microenvironments co-assembled by glycans and other macromolecules, and design systematic profiling and intervention strategies for disease diagnosis and therapy — from glycan-editing-enhanced tumour immunity to new cell-surface markers, glycan-mediated interactions, and glycan-enabled biologics.

Tumor immunityBiomarkersGlycan engineering
Featured publication

Highlight paper

Protein Cell 2026, pwag053

O-GlcNAc Clusters in Intrinsically Disordered Regions Regulate Transcriptional Condensates and Gene Control

We identify a previously unappreciated regulatory role of O-GlcNAc clusters located within intrinsically disordered regions of transcriptional regulators. These glycan clusters modulate the material properties of transcriptional condensates and downstream gene-control programmes.

O-GlcNAcBiomolecular condensatesTranscription
Join us

Want to help us read the language of glycans?

We are recruiting postdocs, PhD students, jointly-supervised PhD students, and research assistants. Reach out to discuss.