Publications by authors named "Jaroslaw Konczak"

Article Synopsis
  • The human antibody repertoire is incredibly vast, theoretically containing over 10 billion potential antibodies, but identifying specific subsets for therapeutic use is crucial.
  • Researchers created the AbNGS database, compiling data from 135 human bioprojects with billions of antibody sequences, highlighting the presence of 270,000 unique complementarity-determining region (CDR-H3) sequences that are common across multiple individuals.
  • These findings suggest that a small portion of these 'public' CDR-H3s can inform and accelerate the design of therapeutic antibodies, potentially making drug development more efficient.
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Antibodies are proteins produced by our immune system that have been harnessed as biotherapeutics. The discovery of antibody-based therapeutics relies on analyzing large volumes of diverse sequences coming from phage display or animal immunizations. Identification of suitable therapeutic candidates is achieved by grouping the sequences by their similarity and subsequent selection of a diverse set of antibodies for further tests.

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AlphaFold2 has hallmarked a generational improvement in protein structure prediction. In particular, advances in antibody structure prediction have provided a highly translatable impact on drug discovery. Though AlphaFold2 laid the groundwork for all proteins, antibody-specific applications require adjustments tailored to these molecules, which has resulted in a handful of deep learning antibody structure predictors.

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