ArticleBioinformatics (Oxford, England)2018
iCFN: an efficient exact algorithm for multistate protein design.
Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Optimizing the breadth of SARS-CoV-2-neutralizing antibodies in vivo and in silico.Human vaccines & immunotherapeutics · 2025Review
- Integrated antibody language model accelerates IgG screening and design for broad-spectrum antiviral therapy.iScience · 2025Article
- Somatic estrogen receptor α mutations that induce dimerization promote receptor activity and breast cancer proliferation.The Journal of clinical investigation · 2024Article
- Computational Design of Miniprotein Binders.Methods in molecular biology (Clifton, N.J.) · 2022Article
- Knowledge-Based Unfolded State Model for Protein Design.Methods in molecular biology (Clifton, N.J.) · 2022Article
- Rosetta:MSF:NN: Boosting performance of multi-state computational protein design with a neural network.PloS one · 2021Article
- De Novo Protein Design for Novel Folds Using Guided Conditional Wasserstein Generative Adversarial Networks.Journal of chemical information and modeling · 2020Article
- Adaptive landscape flattening allows the design of both enzyme: Substrate binding and catalytic power.PLoS computational biology · 2020Article
- Evaluating the predictions of the protein stability change upon single amino acid substitutions for the FXN CAGI5 challenge.Human mutation · 2019Article
- Predicting pathogenicity of missense variants with weakly supervised regression.Human mutation · 2019Article
- Engineering a HER2-specific antibody-drug conjugate to increase lysosomal delivery and therapeutic efficacy.Nature biotechnology · 2019Article
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Authors and funding
2 authors.
Funding
Abstract
Motivation: Multistate protein design addresses real-world challenges, such as multi-specificity design and backbone flexibility, by considering both positive and negative protein states with an ensemble of substates for each. It also presents an enormous challenge to exact algorithms that guarantee the optimal solutions and enable a direct test of mechanistic hypotheses behind models. However, efficient exact algorithms are lacking for multistate protein design. Results: We have developed an efficient exact algorithm called interconnected cost function networks (iCFN) for multistate protein design. Its generic formulation allows for a wide array of applications such as stability, affinity and specificity designs while addressing concerns such as global flexibility of protein backbones. iCFN treats each substate design as a weighted constraint satisfaction problem (WCSP) modeled through a CFN; and it solves the coupled WCSPs using novel bounds and a depth-first branch-and-bound search over a tree structure of sequences, substates, and conformations. When iCFN is applied to specificity design of a T-cell receptor, a problem of unprecedented size to exact methods, it drastically reduces search space and running time to make the problem tractable. Moreover, iCFN generates experimentally-agreeing receptor designs with improved accuracy compared with state-of-the-art methods, highlights the importance of modeling backbone flexibility in protein design, and reveals molecular mechanisms underlying binding specificity. Availability and implementation: https://shen-lab.github.io/software/iCFN. Supplementary information: Supplementary data are available at Bioinformatics online.
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