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Mattox, D. E.

Publications and source records attributed to Mattox, D. E..

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Attention please: modeling global and local context in glycan structure-function relationships

Glycans are found across the tree of life with remarkable structural diversity enabling critical contributions to diverse biological processes, ranging from facilitating host-pathogen interactions to regulating mitosis & DNA damage repair. While functional motifs within glycan structures are largely responsible for mediating interactions, the contexts in which the motifs are presented can drastically impact these interactions and their downstream effects. Here, we demonstrate the first deep learning method to represent both local and global context in the study of glycan structure-function relationships. Our method, glyBERT, encodes glycans with a branched biochemical language and employs an attention-based deep language model to learn biologically relevant glycan representations focused on the most important components within their global structures. Applying glyBERT to a variety of prediction tasks confirms the value of capturing rich context-dependent patterns in this attention-based model: the same monosaccharides and glycan motifs are represented differently in different contexts and thereby enable improved predictive performance relative to the previous state-of-the-art approaches. Furthermore, glyBERT supports generative exploration of context-dependent glycan structure-function space, moving from one glycan to "nearby" glycans so as to maintain or alter predicted functional properties. In a case study application to altering glycan immunogenicity, this generative process reveals the learned contextual determinants of immunogenicity while yielding both known and novel, realistic glycan structures with altered predicted immunogenicity. In summary, modeling the context dependence of glycan motifs is critical for investigating overall glycan functionality and can enable further exploration of glycan structure-function space to inform new hypotheses and synthetic efforts.

bioinformatics↗

Comprehensive analysis of lectin-glycan interactions reveals determinants of lectin specificity

Lectin-glycan interactions facilitate inter- and intracellular communication in many processes including protein trafficking, host-pathogen recognition, and tumorigenesis promotion. Specific recognition of glycans by lectins is also the basis for a wide range of applications in areas including glycobiology research, cancer screening, and antiviral therapeutics. To provide a better understanding of the determinants of lectin-glycan interaction specificity and support such applications, this study comprehensively investigates specificity-conferring features of all available lectin-glycan complex structures. Systematic characterization, comparison, and predictive modeling of a set of 221 complementary physicochemical and geometric features representing these interactions highlighted specificity-conferring features with potential mechanistic insight. Univariable comparative analyses with weighted Wilcoxon-Mann-Whitney tests revealed strong statistical associations between binding site features and specificity that are conserved across unrelated lectin binding sites. Multivariable modeling with random forests demonstrated the utility of these features for predicting the identity of bound glycans based on generalized patterns learned from non-homologous lectins. These analyses revealed global determinants of lectin specificity, such as sialic acid glycan recognition in deep, concave binding sites enriched for positively charged residues, in contrast to high mannose glycan recognition in fairly shallow but well-defined pockets enriched for non-polar residues. Focused analysis of hemagglutinin interactions with human-like and avian-like glycans uncovered features representing both known and novel mutations related to shifts in influenza tropism from avian to human tissues. The presented systematic characterization of lectin binding sites provides a novel approach to studying lectin specificity and is a step towards confidently predicting new lectin-glycan interactions. AUTHOR SUMMARYGlycans are sugar molecules found attached to many proteins and coating the outsides of cells from most organisms. Specific recognition of glycans by proteins called lectins facilitates many biological processes, for example enabling influenza to gain access to cells, helping the immune system recognize pathogens, and sorting newly built proteins for transport to appropriate cellular regions. Understanding what makes a particular lectin consider a particular glycan "sweeter" than the vast set of other glycans can help us better understand these processes and how to monitor and control them. To that end, we systematically characterized the sites on lectin structures where glycans are bound, breaking down molecular structures into a comprehensive set of biochemical and geometric features summarizing the sites. This enabled us to discover statistical relationships between binding site features and the glycans recognized by the sites, and further to be able to predict, from a lectin structure, which glycans it recognizes. For the first time, we are able to demonstrate that there are general features of lectin binding sites correlated with and predictive of their specificities, even in unrelated lectins. Ultimately, these findings can help us discover and engineer new lectins for use in research, diagnostics, or even therapeutics.

bioinformatics↗