{"title":"Various challenges in understanding the thick filaments, within and outside skeletal and cardiac muscles.","authors":"Jean Emile Morel","doi":"10.1007/s12551-025-01289-8","DOIUrl":null,"url":null,"abstract":"<p><p>Thick filaments isolated from various sources, most frequently skeletal and cardiac muscles, have been studied, but several aspects of their behavior remain to be clarified. Myosin II is the principal component of these filaments. A \"traditional\" interacting-heads motif (IHM) has been observed in isolated thick filaments. In this motif, the two heads of the myosin II molecule interact and are stuck to the backbone of the filaments. Another aspect, the super-relaxed state (SRX state), has been described in situ, in relaxed demembranated muscle fibers and myofibrils. It has frequently been claimed that the IHM and the SRX state are closely related. Some authors still consider this relationship valid, but this view is now broadly called into question. These two phenomena occur in very different conditions, making it difficult to determine if and how they are related. For example, macromolecular crowding is a characteristic feature in situ (regardless of interfilament spacing), but not in the conditions in which the \"traditional\" IHM has been observed. Recent studies in situ have attempted to resolve this problem, but some of the reported findings conflict. Moreover, the association of other proteins with the myosin filaments in situ increases thick filament complexity. Experimental conditions may affect the results obtained but the consideration of long-overlooked data would help to prevent erroneous interpretations. For instance, neither the absence (EM studies) or presence (in situ studies) of cell-associated water nor electrical charges are taken into account in any of the published studies in this domain and the omission of these two parameters could lead to contradictory conclusions. My principal objective here is to provide a brief overview (with a limited number of illustrative references) of the increasing complexity of our understanding of thick filaments over the years, particularly as concerns the weak coupling or absence of coupling between the IHM and the SRX state (recent findings that may be difficult to interpret).</p>","PeriodicalId":9094,"journal":{"name":"Biophysical reviews","volume":"17 3","pages":"829-834"},"PeriodicalIF":3.7000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12290140/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysical reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12551-025-01289-8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Thick filaments isolated from various sources, most frequently skeletal and cardiac muscles, have been studied, but several aspects of their behavior remain to be clarified. Myosin II is the principal component of these filaments. A "traditional" interacting-heads motif (IHM) has been observed in isolated thick filaments. In this motif, the two heads of the myosin II molecule interact and are stuck to the backbone of the filaments. Another aspect, the super-relaxed state (SRX state), has been described in situ, in relaxed demembranated muscle fibers and myofibrils. It has frequently been claimed that the IHM and the SRX state are closely related. Some authors still consider this relationship valid, but this view is now broadly called into question. These two phenomena occur in very different conditions, making it difficult to determine if and how they are related. For example, macromolecular crowding is a characteristic feature in situ (regardless of interfilament spacing), but not in the conditions in which the "traditional" IHM has been observed. Recent studies in situ have attempted to resolve this problem, but some of the reported findings conflict. Moreover, the association of other proteins with the myosin filaments in situ increases thick filament complexity. Experimental conditions may affect the results obtained but the consideration of long-overlooked data would help to prevent erroneous interpretations. For instance, neither the absence (EM studies) or presence (in situ studies) of cell-associated water nor electrical charges are taken into account in any of the published studies in this domain and the omission of these two parameters could lead to contradictory conclusions. My principal objective here is to provide a brief overview (with a limited number of illustrative references) of the increasing complexity of our understanding of thick filaments over the years, particularly as concerns the weak coupling or absence of coupling between the IHM and the SRX state (recent findings that may be difficult to interpret).
期刊介绍:
Biophysical Reviews aims to publish critical and timely reviews from key figures in the field of biophysics. The bulk of the reviews that are currently published are from invited authors, but the journal is also open for non-solicited reviews. Interested authors are encouraged to discuss the possibility of contributing a review with the Editor-in-Chief prior to submission. Through publishing reviews on biophysics, the editors of the journal hope to illustrate the great power and potential of physical techniques in the biological sciences, they aim to stimulate the discussion and promote further research and would like to educate and enthuse basic researcher scientists and students of biophysics. Biophysical Reviews covers the entire field of biophysics, generally defined as the science of describing and defining biological phenomenon using the concepts and the techniques of physics. This includes but is not limited by such areas as: - Bioinformatics - Biophysical methods and instrumentation - Medical biophysics - Biosystems - Cell biophysics and organization - Macromolecules: dynamics, structures and interactions - Single molecule biophysics - Membrane biophysics, channels and transportation