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The advent of the electron microscope, the findings of J. David Robertson, the proposal of Singer and Nicolson, and additional work of Unwin and Henderson all contributed to the development of the modern membrane model. However, understanding of past membrane models elucidates present-day perception of membrane characteristics.
Charles Ernest Overton (1865–1933) was a British and Swedish physiologist and biologist, now regarded as a pioneer of the theory of the cell membrane. [1]In the last years of the 19th century Overton did experimental work, allowing the distinction to be drawn between the cell wall of plants and their cytoplasmic membrane. [2]
The results of this experiment were key in the development of the "fluid mosaic" model of the cell membrane by Singer and Nicolson in 1972. [19] According to this model, biological membranes are composed largely of bare lipid bilayer with proteins penetrating either half way or all the way through the membrane.
Fluid mosaic model of a cell membrane. The fluid mosaic model explains various characteristics regarding the structure of functional cell membranes.According to this biological model, there is a lipid bilayer (two molecules thick layer consisting primarily of amphipathic phospholipids) in which protein molecules are embedded.
Anticipating the birth of string theory by almost a decade, he was the first to introduce what is now called a type of Nambu–Goto action for membranes. [2] [3] In the Dirac membrane model the repulsive electromagnetic forces on the membrane are balanced by the contracting ones coming from the positive tension.
The Davson–Danielli model (or paucimolecular model) was a model of the plasma membrane of a cell, proposed in 1935 by Hugh Davson and James Danielli. The model describes a phospholipid bilayer that lies between two layers of globular proteins , which is both trilaminar and lipoprotinious. [ 1 ]
A Nicholson model, showing a short part of protein backbone (white) with side chains (grey). Note the snipped stubs representing hydrogen atoms. A good example of composite models is the Nicholson approach, widely used from the late 1970s for building models of biological macromolecules.
The actin-based membrane skeleton (MSK) meshwork is directly situated on the cytoplasmic surface of the plasma membrane. Membrane skeleton fence, or membrane skeleton corralling model, suggests that this meshwork is likely to partition the plasma membrane into many small compartments with regard to the lateral diffusion of membrane molecules.