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October 1, 2026
HSE Researchers Show How Congenital Motor Disorders Affect Brain Development
Researchers from HSE University’s Institute for Cognitive Neuroscience have synthesised the findings of their previous studies on brain development in children with obstetric brachial plexus palsy and arthrogryposis. Their analysis shows that impaired motor function in early childhood not only limits children’s motor experience but also affects memory, categorical thinking, and information processing. The study has been published in Frontiers in Psychology.
October 1, 2026
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Russian universities, with the participation of HSE University, Sber, and Z-union, have developed a neural network that can simultaneously assess the risk of 15 types of pathology from retinal photographs, including not only eye diseases but also cardiovascular conditions. The AI system can help clinicians detect potentially concerning changes at an early stage, identify signs reflecting the condition of retinal blood vessels, and determine whether a patient may need further examination. The paper has been published in Frontiers in Medicine.
September 30, 2026
'We Did Not Limit the Time for Questions'
The International Laboratory for Supercomputer Atomistic Modelling and Multi-Scale Analysis at HSE University held a major conference on molecular dynamics. Participants had the opportunity to attend all the presentations, while speakers were given as much time as they needed to answer questions. The HSE News Service interviewed Grigory Smirnov, Head of the Laboratory, and Genri Norman, Chief Research Fellow, about the conference preparations and the discussions it generated.

 

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Self-Consistent Framework Connecting Experimental Proxies of Protein Dynamics with Configurational Entropy

Journal of Chemical Theory and Computation. 2018. Vol. 14. P. 3796–3810.
Polyansky A.

The recently developed NMR techniques enable estimation of protein configurational entropy change from the change in the average methyl order parameters. This experimental observable, however, does not directly measure the contribution of intramolecular couplings, protein main-chain motions, or angular dynamics. Here, we carry out a self-consistent computational analysis of the impact of these missing contributions on an extensive set of molecular dynamics simulations of different proteins undergoing binding. Specifically, we compare the configurational entropy change in protein complex formation as obtained by the maximum information spanning tree approximation (MIST), which treats the above entropy contributions directly, and the change in the average NMR methyl and NH order parameters. Our parallel implementation of MIST allows us to treat hard angular degrees of freedom as well as couplings up to full pairwise order explicitly, while still involving a high degree of sampling and tackling molecules of biologically relevant sizes. First, we demonstrate a remarkably strong linear relationship between the total configurational entropy change and the average change in both methyl and backbone-NH order parameters. Second, in contrast to canonical assumptions, we show that the main-chain and angular terms contribute significantly to the overall configurational entropy change and also scale linearly with it. Consequently, linear models starting from the average methyl order parameters are able to capture the contribution of main-chain and angular terms well. After applying the quantum-mechanical harmonic oscillator entropy formalism, we establish a similarly strong linear relationship for X-ray crystallographic B-factors. Finally, we demonstrate that the observed linear relationships remain robust against drastic undersampling and argue that they reflect an intrinsic property of compact proteins. Despite their remarkable strength, however, the above linear relationships yield estimates of configurational entropy change whose accuracy appears to be sufficient for qualitative applications only.

Research target: Computer Science Biology
Language: English
DOI
Keywords: Computational biology
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