A multi-scale analysis of the CzrA transcription repressor highlights the allosteric changes induced by metal ion binding

التفاصيل البيبلوغرافية
العنوان: A multi-scale analysis of the CzrA transcription repressor highlights the allosteric changes induced by metal ion binding
المؤلفون: Rigoli, Marta, Potestio, Raffaello, Menichetti, Roberto
سنة النشر: 2024
المجموعة: Physics (Other)
Quantitative Biology
مصطلحات موضوعية: Quantitative Biology - Biomolecules, Physics - Biological Physics
الوصف: Allosteric regulation is a widespread strategy employed by several proteins to transduce chemical signals and perform biological functions. Metal sensor proteins are exemplary in this respect, e.g., in that they selectively bind and unbind DNA depending on the state of a distal ion coordination site. In this work, we carry out an investigation of the structural and mechanical properties of the CzrA transcription repressor through the analysis of microsecond-long molecular dynamics (MD) trajectories; the latter are processed through the mapping entropy optimisation workflow (MEOW), a recently developed information-theoretical method that highlights, in an unsupervised manner, residues of particular mechanical, functional, and biological importance. This approach allows us to unveil how differences in the properties of the molecule are controlled by the state of the zinc coordination site, with particular attention to the DNA binding region. These changes correlate with a redistribution of the conformational variability of the residues throughout the molecule, in spite of an overall consistency of its architecture in the two (ion-bound and free) coordination states. The results of this work corroborate previous studies, provide novel insight into the fine details of the mechanics of CzrA, and showcase the MEOW approach as a novel instrument for the study of allosteric regulation and other processes in proteins through the analysis of plain MD simulations.
نوع الوثيقة: Working Paper
URL الوصول: http://arxiv.org/abs/2409.03584
رقم الأكسشن: edsarx.2409.03584
قاعدة البيانات: arXiv