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Otten, L.

Publications and source records attributed to Otten, L..

2 recordsLinked to original sources

Negative Cooperativity in a Polybivalent Complex Allows the Prevalence of a Partial Bound State.

The central region of the cytoplasmic dynein complex, comprising the intermediate chain (IC) and two light chains (LC8 and Tctex1), has eluded thorough quantitative characterization due to its participation in a highly coupled seven-state binding network. Although isothermal titration calorimetry (ITC) is the gold standard for measuring binding thermodynamics, conventional analyses are limited to simple interaction schemes because individual isotherms contain insufficient information to resolve complex reaction networks. Here, we overcome this limitation by combining extensive experimental sampling with hierarchical Bayesian inference. We collected 39 ITC isotherms spanning eight experiment types and developed a global Bayesian framework integrating multiple datasets while explicitly accounting for concentration uncertainty. Using this approach, we fit the complete dataset to a mechanistic seven-state model, estimating 190 parameters, including 12 thermodynamic parameters while marginalizing over 178 nuisance parameters. Remarkably, this strategy yields 95% confidence intervals for thermodynamic values as narrow as 0.05 kcal/mol and back-propagates to nanomolar precision in effective concentrations, even when experimental concentrations are in the hundreds of micromolar. The resulting thermodynamic landscape enables predictive modelling of assembly populations under different scenarios, including binding states inaccessible to standard ITC analyses. These results reveal previously unrecognized binding states that may play key roles in dynein cargo attachment and release. More broadly, this work reveals a form of "multi-cooperativity" governing dynein assembly and demonstrates how intensive experimentation coupled with modern statistical tools can resolve complex molecular systems beyond the reach of traditional biophysical techniques. Significance StatementLarge, complex mechanistic processes have remained difficult to fully characterize, which limits interpretability of the underlying biology. We utilize a large dataset of 39 complementary experiments to fully characterize a seven-state system using Bayesian inference. This process achieves impressively precise fits with 0.05 kcal/mol width confidence intervals. The high precision enables assessment of simultaneous positive and negative cooperativity in the assembly of the dynein intermediate chain with its light-chain partners. Simulation of state populations suggests that this balancing cooperativity is finely tuned to allow access to a half-bound state which has been previously inaccessible quantitatively. Our approach is broadly applicable and supports an emerging principle of molecular regulation--negative cooperativity as a strategy for tuning responsiveness and dynamic control.

biophysics↗

Improving parameter inference by resolving Bayesian prior ambiguity via multi-dataset analysis: Application to isothermal titration calorimetry

Isothermal titration calorimetry (ITC) is a powerful technique for probing biomolecular interactions. However, accurate determination of binding parameters--such as enthalpy and free energy--as well as associated uncertainties can be hindered by noise and concentration variability. Notably, the mathematical ambiguity surrounding analyte concentrations in standard binding models intrinsically limits the precision with which binding parameters, particularly binding enthalpies, can be determined. Here, we present a Bayesian pipeline that resolves this ambiguity by combining two key strategies: simultaneous analysis of multiple ITC datasets and a hierarchical Bayesian treatment of analyte concentration priors. This dual approach not only lifts the degeneracy inherent in single-dataset studies but also removes an ambiguity typically present in Bayesian analysis by self-consistently refining concentration estimates, ensuring optimal joint inference of binding parameters and concentrations. Using modern Monte Carlo techniques enables our pipeline to provide robust posterior sampling for more than 10 datasets and 40 total parameters. We validate the approach with synthetic ITC datasets for single- and multi-site binding models and apply it to experimental data, including 14 datasets for 1:1 binding of Mg(II) to the chelator EDTA and multiple datasets of the hub protein LC8 with diverse binding partners. This work serves as a foundation for improving the precision of binding constants using multiple ITC datasets, while providing a systematic framework for assessing the reliability of experimental concentration estimates, paving the way for more accurate biomolecular interaction studies.

biophysics↗