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1.
Phys Chem Chem Phys ; 26(1): 569-580, 2023 Dec 21.
Artigo em Inglês | MEDLINE | ID: mdl-38086647

RESUMO

Understanding the physical principles underlying the structural organization of the proteinaceous viral shells is of major importance to advance antiviral strategies. Here, we develop a phenomenological thermodynamic theory, which considers structures of small and middle-size icosahedral viral shells as a result of condensation of a minimum number of protein density waves on a spherical surface. Each of these irreducible critical waves has icosahedral symmetry and can be expressed as a specific series of the spherical harmonics Ylm with the same wave number l. As we demonstrate, in small viral shells self-assembled from individual proteins, the maxima of one critical density wave determine the positions of proteins, while the spatial derivatives of the second one control the protein orientations on the shell surface. In contrast to the small shells, the middle-size ones are always formed from pentamers and hexamers (referred to as capsomers). Considering all such structures deposited in the Protein Data Bank, we unexpectedly found that the positions of capsomeres in these shells correspond to the maxima of interference patterns produced by no more than two critical waves with close wave numbers. This fact allows us to explain the observed limit size of the icosahedral shells assembled from pentamers and hexamers. We also construct nonequilibrium thermodynamic potentials describing the protein crystallization and discuss the reasons behind the specific handedness of the viral shells.


Assuntos
Proteínas do Capsídeo , Capsídeo , Capsídeo/química , Capsídeo/metabolismo , Proteínas do Capsídeo/química , Vírion
2.
Cell Mol Life Sci ; 77(17): 3453-3464, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31732791

RESUMO

During embryogenesis of all vertebrates, haematopoietic stem/progenitor cells (HSPCs) extrude from the aorta by a complex process named endothelial-to-haematopoietic transition (EHT). HSPCs will then colonize haematopoietic organs allowing haematopoiesis throughout adult life. The mechanism underlying EHT including the role of each aortic endothelial cell (EC) within the global aorta dynamics remains unknown. In the present study, we show for the first time that EHT involves the remodelling of individual cells within a collective migration of ECs which is tightly orchestrated, resulting in HSPCs extrusion in the sub-aortic space without compromising aorta integrity. By performing a cross-disciplinary study which combines high-resolution 4D imaging and theoretical analysis based on the concepts of classical mechanics, we propose that this complex developmental process is dependent on mechanical instabilities of the aorta preparing and facilitating the extrusion of HSPCs.


Assuntos
Aorta/fisiologia , Células-Tronco Hematopoéticas/metabolismo , Amidas/farmacologia , Aminoquinolinas/farmacologia , Animais , Animais Geneticamente Modificados/metabolismo , Embrião não Mamífero/citologia , Embrião não Mamífero/efeitos dos fármacos , Embrião não Mamífero/metabolismo , Células Endoteliais/citologia , Hematopoese , Células-Tronco Hematopoéticas/citologia , Microscopia de Fluorescência , Piridinas/farmacologia , Pirimidinas/farmacologia , Imagem com Lapso de Tempo , Peixe-Zebra/crescimento & desenvolvimento
3.
Sci Rep ; 11(1): 9316, 2021 04 29.
Artigo em Inglês | MEDLINE | ID: mdl-33927284

RESUMO

All blood cells originate from hematopoietic stem/progenitor cells (HSPCs). HSPCs are formed from endothelial cells (ECs) of the dorsal aorta (DA), via endothelial-to-hematopoietic transition (EHT). The zebrafish is a primary model organism to study the process in vivo. While the role of mechanical stress in controlling gene expression promoting cell differentiation is actively investigated, mechanisms driving shape changes of the DA and individual ECs remain poorly understood. We address this problem by developing a new DA micromechanical model and applying it to experimental data on zebrafish morphogenesis. The model considers the DA as an isotropic tubular membrane subjected to hydrostatic blood pressure and axial stress. The DA evolution is described as a movement in the dimensionless controlling parameters space: normalized hydrostatic pressure and axial stress. We argue that HSPC production is accompanied by two mechanical instabilities arising in the system due to the plane stress in the DA walls and show how a complex interplay between mechanical forces in the system drives the emerging morphological changes.


Assuntos
Aorta/fisiologia , Hematopoese , Células-Tronco Hematopoéticas/fisiologia , Modelos Cardiovasculares , Animais , Aorta/diagnóstico por imagem , Aorta/embriologia , Estresse Mecânico , Imagem com Lapso de Tempo , Peixe-Zebra
4.
J Phys Condens Matter ; 31(42): 425302, 2019 Oct 23.
Artigo em Inglês | MEDLINE | ID: mdl-31181549

RESUMO

Synthesis temperatures of composite materials are usually far less than the ones of their use, thus carbon nanotubes (CNTs) embedded into a polymer matrix undergo significant axial stress. We develop a continuous theory, which describes the dynamics of stressed single-walled (SW-) CNTs and predicts their low-frequency phonon spectra. The changes in dispersion laws of SWCNT low-frequency phonon modes due to the axial stress of different signs are discussed. Then, the results obtained are used to analyze low-temperature (T < 70 K) heat capacity and thermal conductivity of individual nanotubes. We demonstrate that compressive stress leads to increase in heat capacity C V of an individual SWCNT, while tensile stress causes C V to decrease. In the latter case at T → 0 heat capacity diminishes according to a linear law ~T instead of a power one ~T 1/2. Nevertheless, according to our results, axial stress hardly affects low-temperature thermal conductance of SWCNTs. Influence of investigated effects on the corresponding macroscopic properties of CNT-based composite materials are also discussed.

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