Interaction-dependent PCR (IDPCR) is a method designed to identify binding pairs from libraries of ligands and targets in a solution-phase experiment. IDPCR relies on the principle that the binding between a DNA-linked ligand and a DNA-linked target brings together complementary DNA sequences, allowing them to form a duplex. This duplex can then be extended by polymerase, resulting in a DNA strand that contains the sequence information for both the ligand and the target, which is subsequently amplified by PCR. This selective amplification enables the identification of specific ligand-target interactions with high sensitivity and specificity.
At CD BioGlyco, our IDPCR-based DEGL screening service employs the innovative IDPCR method for high-throughput glycan screening. In this process, each glycan in the library is linked to a unique DNA sequence, forming the DEGL. When these glycans bind to a target of interest, IDPCR selectively amplifies the DNA sequences corresponding to the binding pairs. This amplification enables the rapid and efficient identification of glycan-binding proteins or other target molecules, which is crucial for the discovery of new glycan-based therapeutics and diagnostics. The service is designed to streamline the identification process, providing valuable insights into glycan interactions that can drive the development of novel medical and research applications.
A vast library of glycans is synthesized, each attached to a unique DNA sequence that serves as a molecular barcode. This forms the DEGL.
The library is incubated with a target of interest (e.g., a protein). Glycans that interact with the target will bind, forming glycan-target complexes.
The DNA sequences attached to the bound glycans are selectively amplified using IDPCR. This step enriches the library for glycans that have successfully interacted with the target.
The amplified DNA is sequenced to identify which glycans in the library have bound to the target. These glycans can then be further analyzed for their potential biological applications.
Technology: IDPCR, High-throughput screening, Drug discovery
Journal: Journal of the American Chemical Society
IF: 11.4
Published: 2014
Results: The study demonstrated the effectiveness of IDPCR as a powerful tool for identifying ligand-target interactions in a solution-phase experiment. By linking ligands and targets to DNA sequences, IDPCR selectively amplifies only those sequences that represent successful binding events. This technique proved to be highly sensitive and capable of enriching DNA sequences corresponding to ligand-target pairs by over 100-fold in the presence of a large excess of nonbinding molecules. The results show that IDPCR can detect a wide range of interactions, including those with varying affinities, making it a versatile method for high-throughput screening of small molecule libraries against multiple targets simultaneously. This method significantly enhances the efficiency of discovering new ligands and understanding their binding specificities across a broad range of targets, offering valuable insights for drug discovery and molecular biology research.
At CD BioGlyco, our DEGL screening service seeks to uncover complex glycan interactions with unparalleled precision. This service leverages cutting-edge IDPCR technology to rapidly and efficiently identify glycan-binding targets, facilitating breakthroughs in drug discovery, biomarker identification, and vaccine development. Please feel free to
to discover how we can support your glycan-related research.Reference
Our mission is to provide comprehensive solutions for glycan research, from library design and high-throughput screening to detailed data analysis and validation.