Liquid Glycan Array (LiGA)

A High-Throughput Discovery Platform for Glycan-Based Targeting

In collaboration with

Multiplexed Screening

Rapid profiling of complex glycan libraries

Biologically Relevant Mapping

Multivalent, in vivo compatible platform for any biological target

Encoded Glycomics

Decoding glycan interactions through DNA-barcoding and NGS

Glycans are not just decorations on the cell surface; they interact with proteins to initiate a wide array of critical biological processes and cellular communication. By leveraging these interactions to trigger receptor-mediated endocytosis, researchers can exploit glycan-binding pathways for the precise, targeted delivery of therapeutic agents.

Several FDA-approved RNA-based therapies–including Givosiran, Lumasiran, and Inclisiran–already rely on GalNAc-ASGPR binding to deliver drugs to the liver. This ability to guide molecules to specific tissue has opened the door to more effective and less toxic treatments.

However, unlocking the full potential of glycan-based targeting requires going beyond hepatocytes. To harness the promise of precision delivery across the entire body, researchers need tools that can rapidly map ligand-cell interactions directly in complex biological environments.

What is LiGA?

Liquid Glycan Array (LiGA) is a platform that presents a multivalent display of glycans on a DNA-barcoded bacteriophage scaffold. Each glycan is uniquely tagged, encoding both its chemical identity and surface density. This multiplexed approach allows thousands of glycan-protein interactions to be tracked in parallel – transforming complex binding profiles into precise, scalable, and easily decoded data.

Multivalent glycan display on DNA-barcoded bacteriophage scaffold

Multiplexed binding assay interrogating glycan-protein interactions in parallel

Why use LiGA?

Save Time

Parallel screening hundreds of interactions at the same time. Uses standard qPCR or NGS to obtain binding data.

Apply on Complex Cellular Environments

Decode glycan-binding interactions on cells both in vitro and in vivo.

Learn More

Discover the effect of multivalency and surface density on glycan binding.

Inject LiGA

In vivo screening

Extract desired cell type

Perform analysis

How to use LiGA

Step 1

Incubate cells/proteins with LiGA

Binding takes place in about one hour and it can be performed at phisiological conditions.

Step 2

Wash unbound particles

Washing conditions ensures non-binders are removed and enriches glycan-phage conjugates of high-affinity.

Step 3

Elute bound particles and PCR

Enrichment of DNA sequencs associated with glycan ligand is decoded by NGS.

Products

Please contact us to see our available products and to discuss your needs. Representative LiGA products below:

α-D-GalNAc-Butyl-Carboxylic Acid

From AG142000

β-D-GalNAc-Butyl-Carboxylic Acid

From AG142005

β-GalNAc-PEG3-Azide

From PE134010

Tris-GalNAc-PEG5-COOH

From MV100054

α-D-Man-Butyl-Carboxylic Acid

From AG642000

α-Man-PEG4-Acid

From PE642000

α-L-Rha-Ethyl-Azide

From AG824005

α-Man-PEG3-Azide

From PE634000

β-D-Gal-Butyl-Carboxylic Acid

From AG442000

β-D-Glc-Butyl-Carboxylic Acid

From AG542000

The Future of Targeted Delivery Starts with Glycans

Let’s start a conversation about how we can bring your project to life.