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Sebastian Deindl

Publications and source records attributed to Sebastian Deindl.

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Protein Dynamics Beyond Structure Prediction

The ability to predict protein three-dimensional structures from amino acid sequences is a landmark achievement in molecular biology, where recent deep learning approaches such as AlphaFold are the culmination of decades of work. Yet, the quantitative understanding of how protein sequences give rise to dynamic conformational changes and higher-order assemblies remains unsolved. Folding and conformational states are dynamic, stochastic processes, shaped by sequence, energy, co-translational constraints, chaperone machineries, and the physicochemical conditions of the cellular environment. Recent advances now position the field to move beyond static structural endpoints toward a mechanistic understanding of folding dynamics in living systems. Single-molecule techniques enable time-resolved observation of folding trajectories and intermediate states hitherto hidden by traditional structural biology approaches, while computational innovations and data-driven approaches offer new ways to integrate heterogeneous data across scales. In this Roadmap, we review the current conceptual landscape of protein folding, examine the experimental and theoretical gaps that remain, and discuss emerging strategies that integrate high-resolution measurements with multiscale modeling. We outline a roadmap toward a quantitative and predictive science of protein folding dynamics, conformational kinetics, and macromolecular self-assembly. Realizing this vision would transform our understanding of the dynamics of molecular self-organization, from the folding of individual polypeptides to the emergence of dynamic macromolecular complexes. This will enable rational control of folding and misfolding in health and disease, extend protein engineering principles beyond static structural design, and establish a mechanistic foundation for predictive and personalized interventions in proteostasis-related disorders.

q-bio.BM

A nanopore-gated sub-attoliter silicon nanocavity for single-molecule trapping and analysis

Biomolecules exhibit dynamic conformations critical to their functions, yet observing these processes at the single-molecule level under native conditions remains a formidable challenge. While surface immobilization has been widely used to extend observation times, it could disrupt molecular dynamics and impede biological function. Moreover, the study of weak molecular interactions requires high local concentrations, often leading to problems with signal saturation in fluorescence-based approaches. Recent advancements in single-molecule trapping techniques have addressed some limitations, but achieving precise, controllable, long-term trapping in a molecularly crowded environment without external forces remains difficult. Here, we introduce a nanopore-gated sub-attoliter silicon nanocavity that enables precise, non-perturbative trapping of individual biomolecules for extended observation times, eliminating the need for external forces. Using nucleosomes as model systems, we demonstrate single-molecule F\"orster resonance energy transfer (smFRET) to monitor relative distances. Our data also show that an applied electric field can modulate the conformational properties of macromolecules, emphasizing a key advantage of our device: it does not require an electric field to retain trapped molecules. We envision this nanocavity platform as a powerful tool for interrogating molecular dynamics in physiologically relevant environments, offering unperturbed access to weak and transient interactions that are central to biological regulation.

physics.ins-det