Mechanosensitive Machinery

Mechanosensitive machinery comprises the proteins and molecular assemblies that detect and respond to physical forces in living cells and tissues. Mechanical inputs such as membrane tension, compression, or shear can deform sensor proteins, trigger conformational changes, and regulate ion flux, cytoskeletal organization, or intracellular signaling. In biology, these systems convert mechanical stimuli into biochemical responses that influence cell shape, migration, growth, and tissue organization. Their study helps explain processes ranging from touch and hearing to vascular function and developmental patterning, while informing research on mechanotransduction, disease mechanisms, biomaterials, and therapies that target force-sensitive cellular pathways.

Mechanosensitive Machinery - Related Videos

Education

JoVE Core - Cell Biology

Protein Translocation Machinery on the ER Membrane

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2023

The translocon complex situated on the ER membrane is the main gateway for the protein secretory pathway. It facilitates the transport of nascent peptides into the ER lumen and their insertion into the ER membrane. Sec61 protein conducting channel In eukaryotes, the translocon complex comprises a core heterotrimeric translocator channel called the Sec61 complex. This channel includes three transmembrane proteins, Sec61α, Sec61β, and Sec61γ, and is the largest subunit of the translocon complex.

Research

JoVE Journal - Biology
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Small-scale Nuclear Extracts for Functional Assays of Gene-expression Machineries

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Cited by 37 •

2012

A protocol for preparation of robust, small-scale HeLa nuclear extracts is described. This protocol is valuable for assays that require use of small populations of cells, such as cells treated with drugs or RNAi. The method should be applicable to a wide variety of gene expression assays and other cell types, including patient cells.

The Encapsulation of Cell-free Transcription and Translation Machinery in Vesicles for the Construction of Cellular Mimics

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Cited by 12 •

2013

Herein we describe simple methods for the preparation of vesicles, the encapsulation of transcription and translation machinery, and the monitoring of protein production. The resulting cell-free systems can be used as a starting point from which to build increasingly complex cellular mimics.

Super-resolution Imaging of the Bacterial Division Machinery

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Cited by 17 •

2013

We describe a super-resolution imaging method to probe the structural organization of the bacterial FtsZ-ring, an essential apparatus for cell division. This method is based on quantitative analyses of photoactivated localization microscopy (PALM) images and can be applied to other bacterial cytoskeletal proteins.

Yeast Luminometric and Xenopus Oocyte Electrophysiological Examinations of the Molecular Mechanosensitivity of TRPV4

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Cited by 13 •

2013

To complement commonly used methods to study TRPV4’s, two methods are described: Its mechanosensitivity can be studied by Ca2+-aequorin luminometry in transgenic yeast upon hypo-osmotic challenge. It can also be examined in TRPV4-RNA injected Xenopus oocytes by whole-cell two-electrode voltage clamp or patch clamp in on-cell or excised mode.

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