{"title":"nath - luxury原理:通过ATP合成/水解的分子组装和非遍历性的统一热力学框架。","authors":"P. Venegas-Aravena , E.G. Cordaro","doi":"10.1016/j.biosystems.2025.105481","DOIUrl":null,"url":null,"abstract":"<div><div>Nath's principle posits that the maximization of free energy dissipation (<span><math><mrow><mi>Φ</mi></mrow></math></span>) under specific constraints facilitates the function and assembly of complex organic molecules under specific constraints, challenging the classical view that increased dissipation leads to disorder. To ground this principle in thermodynamics, this study establishes a connection between Nath's principle and a principle applicable beyond biological systems: the Principium Luxuri<em>æ</em>. The latter describes how multiscale systems dissipate energy in response to external forces. The conceptual equivalence of both principles is demonstrated, supporting Nath's unified theory of ATP synthesis/hydrolysis and the existence of non-equilibrium mechanisms for cellular energy dissipation, conservation, and storage. This connection is reinforced by a mathematical relationship demonstrating a negative correlation between <span><math><mrow><mi>Φ</mi></mrow></math></span> and the thermodynamic fractal dimension (<span><math><mrow><mi>D</mi></mrow></math></span>), a parameter quantifying multiscale dissipation in the Principium Luxuri<em>æ</em>. Furthermore, a relationship is established between the equations governing homeostasis and free energy. Given that the multiscale description is predicated on constraints imposed by external forces, which limit possible molecular configurations, the non-ergodic nature of biological systems described by Nath's principle is validated. A comparative analysis is conducted, contrasting these Nath-Luxuri<em>æ</em> principles with Prigogine's work (which describes ergodic systems) in their application to the thermodynamic evolution of biological systems and the constraints present on Earth for the formation of life. It is suggested that the Nath-Luxuri<em>æ</em> principles may significantly enhance the probability of assembling complex molecules necessary for life.</div></div>","PeriodicalId":50730,"journal":{"name":"Biosystems","volume":"253 ","pages":"Article 105481"},"PeriodicalIF":2.0000,"publicationDate":"2025-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Nath-Luxuriæ principles: Unified thermodynamic framework for molecular assembly and non-ergodicity via ATP synthesis/hydrolysis example\",\"authors\":\"P. Venegas-Aravena , E.G. Cordaro\",\"doi\":\"10.1016/j.biosystems.2025.105481\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Nath's principle posits that the maximization of free energy dissipation (<span><math><mrow><mi>Φ</mi></mrow></math></span>) under specific constraints facilitates the function and assembly of complex organic molecules under specific constraints, challenging the classical view that increased dissipation leads to disorder. To ground this principle in thermodynamics, this study establishes a connection between Nath's principle and a principle applicable beyond biological systems: the Principium Luxuri<em>æ</em>. The latter describes how multiscale systems dissipate energy in response to external forces. The conceptual equivalence of both principles is demonstrated, supporting Nath's unified theory of ATP synthesis/hydrolysis and the existence of non-equilibrium mechanisms for cellular energy dissipation, conservation, and storage. This connection is reinforced by a mathematical relationship demonstrating a negative correlation between <span><math><mrow><mi>Φ</mi></mrow></math></span> and the thermodynamic fractal dimension (<span><math><mrow><mi>D</mi></mrow></math></span>), a parameter quantifying multiscale dissipation in the Principium Luxuri<em>æ</em>. Furthermore, a relationship is established between the equations governing homeostasis and free energy. Given that the multiscale description is predicated on constraints imposed by external forces, which limit possible molecular configurations, the non-ergodic nature of biological systems described by Nath's principle is validated. A comparative analysis is conducted, contrasting these Nath-Luxuri<em>æ</em> principles with Prigogine's work (which describes ergodic systems) in their application to the thermodynamic evolution of biological systems and the constraints present on Earth for the formation of life. It is suggested that the Nath-Luxuri<em>æ</em> principles may significantly enhance the probability of assembling complex molecules necessary for life.</div></div>\",\"PeriodicalId\":50730,\"journal\":{\"name\":\"Biosystems\",\"volume\":\"253 \",\"pages\":\"Article 105481\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-05-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biosystems\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0303264725000917\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosystems","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0303264725000917","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
The Nath-Luxuriæ principles: Unified thermodynamic framework for molecular assembly and non-ergodicity via ATP synthesis/hydrolysis example
Nath's principle posits that the maximization of free energy dissipation () under specific constraints facilitates the function and assembly of complex organic molecules under specific constraints, challenging the classical view that increased dissipation leads to disorder. To ground this principle in thermodynamics, this study establishes a connection between Nath's principle and a principle applicable beyond biological systems: the Principium Luxuriæ. The latter describes how multiscale systems dissipate energy in response to external forces. The conceptual equivalence of both principles is demonstrated, supporting Nath's unified theory of ATP synthesis/hydrolysis and the existence of non-equilibrium mechanisms for cellular energy dissipation, conservation, and storage. This connection is reinforced by a mathematical relationship demonstrating a negative correlation between and the thermodynamic fractal dimension (), a parameter quantifying multiscale dissipation in the Principium Luxuriæ. Furthermore, a relationship is established between the equations governing homeostasis and free energy. Given that the multiscale description is predicated on constraints imposed by external forces, which limit possible molecular configurations, the non-ergodic nature of biological systems described by Nath's principle is validated. A comparative analysis is conducted, contrasting these Nath-Luxuriæ principles with Prigogine's work (which describes ergodic systems) in their application to the thermodynamic evolution of biological systems and the constraints present on Earth for the formation of life. It is suggested that the Nath-Luxuriæ principles may significantly enhance the probability of assembling complex molecules necessary for life.
期刊介绍:
BioSystems encourages experimental, computational, and theoretical articles that link biology, evolutionary thinking, and the information processing sciences. The link areas form a circle that encompasses the fundamental nature of biological information processing, computational modeling of complex biological systems, evolutionary models of computation, the application of biological principles to the design of novel computing systems, and the use of biomolecular materials to synthesize artificial systems that capture essential principles of natural biological information processing.