ArticleMethods in molecular biology (Clifton, N.J.)2025
High-Throughput Epitope Binning Analysis of Human Monoclonal Antibodies to Assess Epitope Diversity Using the Octet Bio-Layer Interferometry Platform.
Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An epitope can be defined as a molecular region on the surface of an antigen capable of eliciting an immune response. Epitope binning, also termed cross-competition assays, provides a method by which large antibody panels usually generated in antibody discovery programs are funneled down during the selection of lead molecules. Antibody binning can therefore be used in early-stage discovery of therapeutic mAbs to sort large panels into "bins" based on their ability to "block" one another's binding to their specific antigen in a pairwise and combinatorial fashion. Selecting mAb clones with affinity to a wide range of epitopes increases the likelihood of choosing functionally relevant candidates.Octet® BLI technology is a biosensor-based automated, real-time, label-free analysis platform suitable for performing epitope binning analysis as a "setup-and-walk away" assay with both moderate-throughput and high-throughput capabilities.BLI platforms are based on the simple format of "dip and read." In this format, sample handling relies on the movement of the disposable fiber optics-based tips containing the sensing surface into samples presented in a standard sample plate. The sampling method is advantageous over similar label-free techniques such as surface plasmon resonance (SPR) in that it allows for the specific analysis of target molecules within a crude sample such as cell culture supernatants, serum, or even plasma without the need to purify samples as sample clogging is not an issue.This chapter discusses the different epitope binning assay formats, the advantages and limitations of each, key aspects of assay development, and the advantages that the Octet® BLI platform offers over techniques such as surface plasmon resonance (SPR).
Indexed as
Identifiers
40593428What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.