» Articles » PMID: 35328477

Small Angle X-ray Diffraction As a Tool for Structural Characterization of Muscle Disease

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2022 Mar 25
PMID 35328477
Authors
Affiliations
Soon will be listed here.
Abstract

Small angle X-ray fiber diffraction is the method of choice for obtaining molecular level structural information from striated muscle fibers under hydrated physiological conditions. For many decades this technique had been used primarily for investigating basic biophysical questions regarding muscle contraction and regulation and its use confined to a relatively small group of expert practitioners. Over the last 20 years, however, X-ray diffraction has emerged as an important tool for investigating the structural consequences of cardiac and skeletal myopathies. In this review we show how simple and straightforward measurements, accessible to non-experts, can be used to extract biophysical parameters that can help explain and characterize the physiology and pathology of a given experimental system. We provide a comprehensive guide to the range of the kinds of measurements that can be made and illustrate how they have been used to provide insights into the structural basis of pathology in a comprehensive review of the literature. We also show how these kinds of measurements can inform current controversies and indicate some future directions.

Citing Articles

A FRET assay to quantitate levels of the human β-cardiac myosin interacting heads motif based on its near-atomic resolution structure.

Goluguri R, Guhathakurta P, Nandwani N, Dawood A, Yakota S, Roopnarine O bioRxiv. 2024; .

PMID: 39713291 PMC: 11661104. DOI: 10.1101/2024.12.05.626936.


The distinctive mechanical and structural signatures of residual force enhancement in myofibers.

Hessel A, Kuehn M, Palmer B, Nissen D, Mishra D, Joumaa V Proc Natl Acad Sci U S A. 2024; 121(52):e2413883121.

PMID: 39680764 PMC: 11670058. DOI: 10.1073/pnas.2413883121.


Mavacamten facilitates myosin head ON-to-OFF transitions and shortens thin filament length in relaxed skeletal muscle.

Kuehn M, Engels N, Nissen D, Freundt J, Ma W, Irving T bioRxiv. 2024; .

PMID: 39677804 PMC: 11642802. DOI: 10.1101/2024.11.29.626031.


Functional role of myosin-binding protein H in thick filaments of developing vertebrate fast-twitch skeletal muscle.

Mead A, Wood N, Nelson S, Palmer B, Yang L, Previs S J Gen Physiol. 2024; 156(12).

PMID: 39373654 PMC: 11461142. DOI: 10.1085/jgp.202413604.


The structural and functional effects of myosin regulatory light chain phosphorylation are amplified by increases in sarcomere length and [Ca].

Turner K, Vander Top B, Kooiker K, Mohran S, Mandrycky C, McMillen T J Physiol. 2024; 602(19):4941-4958.

PMID: 39283968 PMC: 11466700. DOI: 10.1113/JP286802.


References
1.
BORDAS J, Svensson A, Rothery M, LOWY J, Diakun G, Boesecke P . Extensibility and symmetry of actin filaments in contracting muscles. Biophys J. 1999; 77(6):3197-207. PMC: 1300590. DOI: 10.1016/S0006-3495(99)77150-X. View

2.
Yu L, Arata T, Steven A, Naylor G, Gamble R, PODOLSKY R . Structural studies of muscle during force development in various states. Adv Exp Med Biol. 1984; 170:207-20. DOI: 10.1007/978-1-4684-4703-3_19. View

3.
Farman G, Walker J, de Tombe P, Irving T . Impact of osmotic compression on sarcomere structure and myofilament calcium sensitivity of isolated rat myocardium. Am J Physiol Heart Circ Physiol. 2006; 291(4):H1847-55. DOI: 10.1152/ajpheart.01237.2005. View

4.
Lindqvist J, Ma W, Li F, Hernandez Y, Kolb J, Kiss B . Triggering typical nemaline myopathy with compound heterozygous nebulin mutations reveals myofilament structural changes as pathomechanism. Nat Commun. 2020; 11(1):2699. PMC: 7264197. DOI: 10.1038/s41467-020-16526-9. View

5.
MILLMAN B . The filament lattice of striated muscle. Physiol Rev. 1998; 78(2):359-91. DOI: 10.1152/physrev.1998.78.2.359. View