Glycans and glycoconjugates play very important roles in various biological processes such as cell-cell interactions, immune processes, stabilization of proteins, cancer, and other diseases, etc. The development of various types of antibodies using them as therapeutic targets is essential for the development of effective treatments. DEGL is an innovative strategy with important applications in screening antibody-binding ligands in a high-throughput manner. With extensive hands-on experience in identifying antibody targets, CD BioGlyco offers reliable and customized DEGL screening solutions. The diversity and high quality of our DEGLs ensure the highest level of success.
We have extensive research experience in antibody biology and have developed a variety of screening strategies. DEGL screening for antibody target identification includes custom synthesis of DEGLs, affinity screening of target antibodies, decoding and structural analysis of glycans, re-synthesis of non-coding glycans, and validation of binding properties of glycans to target antibodies. The specific screening process is described below:
We chemically synthesize a variety of glycan structures, such as the global-sugar series, according to antibody type and binding characteristics, and achieve DNA-Glycan coupling through click chemistry. Our team custom synthesizes libraries of various orders of magnitude according to client needs to improve hit rates.
DEGL is incubated with a labeled antibody under specific conditions to allow binding interactions to occur between the glycan and the antibody. After incubation, an affinity screen is performed to isolate glycan-DNA affixes that have bound to the antibody and to elute unbound molecules.
DEGL screening is followed by decoding and data analysis. We use polymerase chain reaction (PCR) to amplify the DNA tag and then sequence it to identify the specific glycan structure that binds to the antibody. We use advanced algorithms and bioinformatics tools for efficient processing and high-throughput analysis of screening data.
After decoding the small molecules that bind to the target antibody, we further screen the well-characterized molecules for de-DNA resynthesis by affinity mass spectrometry. Afterward, their binding affinity and biological activity with the antibody target are tested and further characterized to understand the binding mechanism and provide certain optimization insights for subsequent studies.
We provide one-stop experimental services and customized solutions using a diversity of DEGLs to screen antibody-targeted ligands.
Technology: DNA-encoded library (DEL)
Journal: Communications Chemistry
IF: 6.581
Published: 2020
Results: DEL technology is a novel strategy to recognize ligands by synthesizing and screening millions or even billions of coding compounds. The technology introduces different small molecule building blocks with unique DNA tags through synthetic chemistry cycles. Several rounds of affinity selection produce mixtures enriched with target protein binders. Amplification of the DNA region by PCR and NGS allows identification of the structure of the binding molecule. An algorithm was developed in this study: eDESIGNER. this algorithm connects all available small molecule building blocks with chemistry suitable for DNA synthesis to generate the DEL chemo space, which has important applications for comprehensive DEL generation.
Fig.1 Flowchart of eDESIGNER. (Martín, et al., 2020)
CD BioGlyco provides valuable insights into antibody targets and potential therapeutics opportunities in drug discovery and development through rapid, high-throughput identification of glycan structures interacting with antibodies by DEGL screening. Welcome to
for customized screening solutions for DEGL and the identification of antibody targets.Reference
Our mission is to provide comprehensive solutions for glycan research, from library design and high-throughput screening to detailed data analysis and validation.