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Hendrickson, C. L.

Publications and source records attributed to Hendrickson, C. L..

2 recordsLinked to original sources

The Euler Characteristic Transform Enables Classification of Complex Plant Shapes and Prediction of Leaf Venation from Blade Geometry

(1) RationaleQuantifying and predicting plant morphology is central to understanding development and evolution, yet many plant forms lack homologous features required for traditional morphometrics. We apply the Euler Characteristic Transform (ECT), an injective descriptor from topological data analysis, to encode 2D plant shapes. The ECT converts contours into image-like representations that preserve shape information while enabling deep learning. (2) MethodsWe computed ECTs for large datasets of leaf and pavement cell shapes and used convolutional neural networks (CNNs) for classification. We also trained CNNs to approximate the inverse mapping, predicting leaf shape masks from radial ECTs. (3) Key resultsECT-based models achieved high classification accuracy, surpassing previous approaches on millions of herbarium-derived leaves. Notably, grapevine leaf venation was predicted from blade geometry alone, demonstrating that vascular structure is encoded in the outline. (4) Main conclusionThe ECT provides a compact, information-preserving representation of biological shape that integrates naturally with deep learning. It enables both accurate classification and predictive reconstruction, revealing latent morphological information and offering new opportunities to study plant form across scales.

plant biology↗

A multi-modal proteomics strategy for characterizing posttranslational modifications of tumor suppressor p53 reveals many sites but few modified forms

Post-translational modifications (PTMs) are found on most proteins, particularly on \"hub\" proteins like the tumor suppressor p53, which has over 100 possible PTM sites. Substantial crosstalk between PTM sites underlies the ability of such proteins to integrate diverse signals and coordinate downstream responses. However, disentangling the combinatorial explosion in global PTM patterns across an entire protein (\"modforms\") has been challenging, as conventional peptide-based mass spectrometry strategies (so-called \"bottom-up\" MS) destroy such global correlations. Alternatively, direct analysis of intact and modified proteins using \"top-down\" MS retains global information. Here, we applied both strategies to recombinant p53 phosphorylated in vitro with Chk1 kinase, which exhibited 41 modified sites by bottom-up MS, but no more than 8 modified sites per molecule detected by top-down MS. This observation that many low-abundance modifications comprise relatively few modforms above a 1% threshold indicates that endogenous p53 PTM complexity may be more definable than previously thought.

systems biology↗