Publication:
Information flow and allosteric communication in proteins

dc.contributor.coauthorHacisuleyman, Aysima
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.kuauthorErman, Burak
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.date.accessioned2024-11-09T23:26:53Z
dc.date.issued2022
dc.description.abstractBased on Schreiber's work on transfer entropy, a molecular theory of nonlinear information transfer between residue pairs in proteins is developed. The joint distribution function for residue fluctuations required by the theory is expressed in terms of tensor Hermite polynomials that conveniently separate harmonic and nonlinear contributions to information transfer. The harmonic part of information transfer is expressed as the difference between time dependent and independent mutual information. Third order nonlinearities are discussed in detail. The amount and speed of information transfer between residues, which are important for understanding allosteric activity in proteins, are discussed. Mutual information between two residues is commonly used for information transfer. While mutual information shows the maximum amount of information that may be transferred between two residues, it does not explain the actual amount of transfer nor the transfer rate of information. For this, dynamic equations of the system are needed. The solution of the Langevin equation and molecular dynamics trajectories are used in the present work for this purpose. Allosteric communication in human NAD-dependent isocitrate dehydrogenase is studied as an example. Calculations show that several paths contribute collectively to information transfer. Important residues on these paths are identified. Time resolved information transfer between these residues, their amplitudes, and transfer rates, which are in agreement with time resolved ultraviolet resonance Raman measurements in general, are estimated. Peak values of calculated information transfer, similar to 0.01-0.04 bits, are about two orders of magnitude smaller than the information content of residues. They are comparable to mutual information values, however. Estimated transfer rates are in the order of 1-20 megabits per second, and sustained transfer during the activity time-span of proteins may be significant. Information transfer from third order contributions is one to two orders of magnitude smaller than the harmonic terms, showing that harmonic analysis is a good approximation to information transfer. Published under an exclusive license by AIP Publishing.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue18
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume156
dc.identifier.doi10.1063/5.0088522
dc.identifier.eissn1089-7690
dc.identifier.issn0021-9606
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85130062425
dc.identifier.urihttps://doi.org/10.1063/5.0088522
dc.identifier.urihttps://hdl.handle.net/20.500.14288/11623
dc.identifier.wos795703400006
dc.keywordsChemistry, physical
dc.keywordsPhysics, atomic, molecular and chemical
dc.language.isoeng
dc.publisherAip Publishing
dc.relation.ispartofJournal of Chemical Physics
dc.subjectChemistry
dc.subjectPhysical
dc.subjectPhysics
dc.subjectAtomic
dc.subjectMolecular
dc.subjectChemical
dc.titleInformation flow and allosteric communication in proteins
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorErman, Burak
local.publication.orgunit1College of Engineering
local.publication.orgunit2Department of Chemical and Biological Engineering
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relation.isParentOrgUnitOfPublication8e756b23-2d4a-4ce8-b1b3-62c794a8c164
relation.isParentOrgUnitOfPublication.latestForDiscovery8e756b23-2d4a-4ce8-b1b3-62c794a8c164

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