> #biology , #science > Explain the evidence of the fluid mosaic model and the Davson- Danielli model.
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Enock Gideon
2 hours ago

Explain the evidence of the fluid mosaic model and the Davson- Danielli model.

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ChatGPT
2 hours ago
The fluid mosaic model of the cell membrane was proposed by Singer and Nicolson in 1972. This model suggests that the cell membrane is composed of a fluid lipid bilayer in which proteins are embedded, giving it a mosaic-like appearance. The lipid bilayer is made up of phospholipids, which have hydrophilic heads that face outward towards the aqueous environment and hydrophobic tails that face inward towards each other. This structure allows the membrane to be flexible and dynamic, allowing for the movement of molecules and proteins within the membrane.

Evidence supporting the fluid mosaic model includes studies using freeze-fracture electron microscopy, which showed a bilayer structure of the membrane with embedded proteins. Additionally, studies using fluorescence recovery after photobleaching (FRAP) have shown that proteins within the membrane are able to move laterally, further supporting the fluidity of the membrane.

In contrast, the Davson-Danielli model, proposed in 1935, suggested that the cell membrane was composed of a sandwich-like structure with a protein layer on either side of a lipid bilayer. This model was based on early electron microscopy studies that showed a dense protein layer on the outer surface of the membrane. However, further research and advancements in technology have since disproven this model, as it was found that proteins are embedded within the lipid bilayer rather than forming distinct layers on either side.

Overall, the fluid mosaic model is widely accepted as the current model for the structure of the cell membrane, supported by various lines of evidence that demonstrate the dynamic and flexible nature of the membrane.
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Google Gemini AI
2 hours ago
Fluid Mosaic Model

- Electron microscopy: Freeze-fracture replicas of cell membranes show a mosaic of small, round particles embedded in a fluid matrix.
- Fluorescence microscopy: When fluorescent probes are targeted to specific membrane components (e.g., proteins or lipids), they diffuse laterally, indicating the fluidity of the membrane.
- Spin label experiments: Molecules attached to specific membrane components exhibit rotational and lateral diffusion, further supporting membrane fluidity.
- NMR spectroscopy: Lipid and protein molecules in the membrane exhibit high mobility, indicating the dynamic nature of the membrane structure.
- Electrical properties: The membrane shows low electrical resistance and a high capacitance, consistent with a fluid, insulating bilayer.

Davson-Danielli Model

- Electron microscopy: Early electron microscopy images suggested a tripartite structure of the membrane, with two dense layers (presumably protein) separated by a light layer (presumably lipid).
- X-ray diffraction: Diffraction patterns of isolated cell membranes showed two strong bands, consistent with the presence of a bimolecular lipid layer.
- Chemical analysis: Isolated cell membranes contained a significant proportion of protein and lipid, supporting the idea of a protein-lipid sandwich.
- Lipid bilayer stability: Experiments with artificial lipid bilayers showed that they could form stable, self-sealing structures, providing support for the lipid bilayer concept.

Limitations of the Davson-Danielli Model:

- The model did not account for membrane fluidity, which was later demonstrated by experimental evidence.
- It overestimated the rigidity of the membrane and did not fully capture the dynamic interactions between membrane components.
- It did not explain the asymmetric distribution of lipids and proteins in biological membranes.

Resolution of the Two Models:

The fluid mosaic model ultimately replaced the Davson-Danielli model because it more accurately reflected the experimental evidence and provided a more complete understanding of membrane structure and function. The Davson-Danielli model still retains historical significance as a stepping stone in the development of our understanding of cell membranes.
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