
The principal RBC membrane structure is a two-layered shell composed of a cytoplasmic membrane (RBCcm) and a spectrin-based cytoskeleton. The RBCcm is a lipid bilayer that includes phospholipids, sphingolipids, cholesterol, and integral membrane proteins. The cytoskeleton is a two-dimensional structure formed by triangularly arranged spectrin filaments parallel to the RBCcm. The RBC membrane is a critical supplier of oxygen to tissues and plays a crucial role in the mammalian metabolism.
| Characteristics | Values |
|---|---|
| Composition | Lipids and proteins |
| Lipid type | Phospholipids, sphingolipids, cholesterol |
| Protein type | Transmembrane proteins, haemoglobin, spectrin, actin, band-3, glycophorin |
| Structure | Two-layered shell |
| Function | Selective transport of molecules, cell-cell recognition, cell deformability, stability |
| Shape | Discocyte, biconcave |
| Dimensions | Diameter: 6.2-8.2 μm, Thickness: 2-2.5 μm, Surface area: 136 μm2 |
| Volume | 90 fL |
| Count | 20-30 trillion |
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What You'll Learn

The RBC membrane is composed of proteins and lipids
The red blood cell (RBC) membrane, or erythrocyte membrane, is a two-layered structure composed of proteins and lipids. This membrane is essential for the physiological function of red blood cells, providing properties such as deformability and stability.
The RBC membrane is structurally distinct from other cell membranes, exhibiting unique material behaviour. It is composed of a plasma membrane envelope, or cytoplasmic membrane, anchored to a two-dimensional elastic network of skeletal proteins, known as the cytoskeleton. This cytoskeleton is formed by spectrin tetramers, which are connected at actin junctional complexes, creating a sixfold triangular network. The cytoskeleton is tethered to the lipid bilayer, which includes various types of lipids such as phospholipids, sphingolipids, cholesterol, and glycolipids.
Proteins play a crucial role in the RBC membrane structure and function. They are responsible for carrying out specific membrane functions, such as the transport of molecules and cell-cell recognition. Integral membrane proteins, such as band-3 and glycophorin, are embedded within the lipid bilayer, contributing to the membrane's stability and functionality. Additionally, membrane-bound enzymes, such as acidic glycohydrolases and O-GlcNAcase (OGA), are present in the RBC membrane and play important roles in cellular processes.
The RBC membrane's protein and lipid composition also influences its mechanical properties. The membrane's deformability is essential for its ability to change shape as it flows through the microcirculation, optimizing oxygen delivery to tissues. The interaction between lipids and proteins within the lipid bilayer allows the RBC membrane to resist bending while maintaining flexibility. This flexibility is crucial for the cell's ability to withstand shear stress and ensure unimpeded transit through the microvasculature.
In summary, the RBC membrane is a dynamic structure composed of proteins and lipids. This composition is vital for the membrane's functionality, mechanical properties, and interactions with other cells. Understanding the RBC membrane's unique structure is essential for studying red blood cell behaviour and its role in physiological processes.
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Phospholipids are a type of lipid that forms a stable barrier
The cell membrane of a red blood cell (RBC) is composed of proteins and lipids. The fundamental structure of the membrane is the phospholipid bilayer, which forms a stable barrier between two aqueous compartments. Phospholipids are a type of lipid that forms a stable barrier. The RBC membrane is essentially a two-dimensional (2D) structure, comprising a cytoskeleton and a lipid bilayer, tethered together. The lipid bilayer includes various types of phospholipids, sphingolipids, cholesterol, and integral membrane proteins, such as band-3 and glycophorin.
The RBC's two-layered outer shell is composed of a cytoplasmic membrane (RBCcm) tethered to a spectrin cytoskeleton, allowing the cell to be flexible and resistant to shear stress. The RBCcm is tethered to the cytoskeleton via two protein complexes: the ankyrin-based complex and the 4.1R-based complex. The cytoskeleton is a 2D sixfold structure consisting of spectrin tetramers, which are connected at the actin junctional complexes. The cytoskeleton is anchored to the RBCcm through tethering sites formed by two macromolecular complexes of membrane proteins. Both complexes are highly mobile within the lipid bilayer and allow the RBCcm to slide against the cytoskeleton.
The RBC membrane resists bending but cannot sustain in-plane static shear stress as the lipids and proteins diffuse within the lipid bilayer at equilibrium. The RBC membrane's unique material behaviour, including maximum elasticity and absolute structural resistance, is the result of a composite structure where a plasma membrane envelope is anchored to a 2D elastic network of skeletal proteins through the binding sites of the cytoplasmic domains of transmembrane proteins placed in the lipid bilayer.
The phospholipid bilayer is critical to the membrane function of acting as a barrier between two aqueous compartments. Because the interior of the phospholipid bilayer is occupied by hydrophobic fatty acid chains, the membrane is impermeable to water-soluble molecules, including ions and most biological molecules. Cholesterol, which inserts into the bilayer of phospholipids, has distinct effects on membrane fluidity depending on the temperature. At high temperatures, cholesterol interferes with the movement of the phospholipid fatty acid chains, reducing the membrane's permeability to small molecules. At low temperatures, cholesterol prevents membranes from freezing and maintains membrane fluidity by interfering with interactions between fatty acid chains.
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Cholesterol is a major membrane constituent of animal cells
Cholesterol is a major lipid in the plasma membrane of mammalian cells and plays diverse structural and functional roles. Cellular unesterified cholesterol is primarily (up to 90%) localized in the plasma membrane and is essential for its physical integrity. Cholesterol has been implicated in the structural and functional modulation of integral membrane proteins and in the formation of cholesterol-rich membrane domains called membrane (lipid) rafts. It affects the physiological features of the cell membrane by controlling its fluidity and regulating the negative membrane curvature through interaction with phospholipid acyl chains.
Cholesterol is an essential component of animal cell plasma membranes. It is absent in bacteria, but plant cells also lack cholesterol, containing related compounds (sterols) that fulfil a similar function. Cholesterol will not form a membrane by itself but inserts into a bilayer of phospholipids with its polar hydroxyl group close to the phospholipid head groups. Depending on the temperature, cholesterol has distinct effects on membrane fluidity. At high temperatures, cholesterol interferes with the movement of the phospholipid fatty-acid chains, making the outer part of the membrane less fluid and reducing its permeability to small molecules. At low temperatures, cholesterol has the opposite effect: by interfering with interactions between fatty-acid chains, it prevents membranes from freezing and maintains membrane fluidity.
The fundamental structure of the membrane is the phospholipid bilayer, which forms a stable barrier between two aqueous compartments. In the case of the plasma membrane, these compartments are the inside and the outside of the cell. In addition to the phospholipids, the plasma membranes of animal cells contain cholesterol and glycolipids. Cholesterol is a major membrane constituent of animal cells, being present in about the same molar amounts as the phospholipids.
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Glycolipids are found exclusively in the outer leaflet of the plasma membrane
The cell membrane of a red blood cell (RBC) is composed of proteins and lipids. The fundamental structure of the membrane is the phospholipid bilayer, which forms a stable barrier between the inside and outside of the cell. In addition to phospholipids, the plasma membranes of animal cells contain cholesterol and glycolipids.
The RBC membrane is a two-dimensional structure, consisting of a cytoskeleton and a lipid bilayer, which are tethered together. The lipid bilayer includes various types of lipids, such as phospholipids, sphingolipids, cholesterol, and integral membrane proteins. The cytoskeleton is a two-dimensional protein network that shapes the cell and provides structural resistance and flexibility.
The RBC membrane exhibits unique material behaviour due to its composite structure. The plasma membrane envelope is anchored to a two-dimensional elastic network of skeletal proteins through binding sites on the cytoplasmic domains of transmembrane proteins placed within the lipid bilayer. This composite structure confers maximum elasticity and absolute structural resistance to the RBC membrane, allowing it to be both flexible and resistant to shear stress.
In summary, glycolipids are found exclusively in the outer leaflet of the plasma membrane, constituting a minor component of the lipids in the RBC membrane. The RBC membrane's unique properties, such as its elasticity and structural resistance, arise from the interaction between the plasma membrane and the underlying cytoskeleton, which is facilitated by the presence of glycolipids and other membrane components.
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The RBC membrane is a two-dimensional structure
The cell membrane of a red blood cell (RBC) is composed of proteins and lipids. The RBC membrane is a two-dimensional structure, consisting of a cytoskeleton and a lipid bilayer. The lipid bilayer includes various types of lipids, such as phospholipids, sphingolipids, cholesterol, glycolipids, and glycoproteins. The cytoskeleton, on the other hand, is a two-dimensional sixfold structure made up of spectrin tetramers, which are connected at actin junctional complexes.
The RBC membrane's two-dimensional nature is essential for its flexibility and resistance to shear stress. This unique structure allows the cell to change shape as it moves through the microvasculature and capillaries, optimizing oxygen delivery to the tissues. The membrane's flexibility is also attributed to the absence of organelles and filaments inside the cell, allowing the lipids and proteins to diffuse within the lipid bilayer at equilibrium.
The RBC membrane's two-dimensional structure is further stabilized by the binding sites of transmembrane proteins, which anchor the lipid bilayer to the cytoskeleton. These transmembrane proteins, such as band-3 and glycophorin, play a crucial role in maintaining the integrity and functionality of the RBC membrane. They contribute to the membrane's deformability and stability, ensuring that it can withstand the demands of blood flow while effectively carrying out its physiological functions.
The two-dimensional nature of the RBC membrane also has implications for its mechanical properties. The arrangement of spectrin filaments in a triangular network contributes to the membrane's elasticity and resistance to bending. However, the RBC membrane cannot sustain in-plane static shear stress, as the diffusion of lipids and proteins within the bilayer affects its overall stability. This dynamic behavior of the RBC membrane is a key area of study, particularly in understanding hereditary blood disorders such as sickle cell disease.
In summary, the RBC membrane's two-dimensional structure is a fundamental aspect of its functionality. The interplay between the cytoskeleton and the lipid bilayer, along with the integral membrane proteins, allows RBCs to perform their critical role in oxygen delivery and carbon dioxide transport efficiently.
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Frequently asked questions
The RBC membrane structure is primarily composed of lipids and proteins.
Lipids are the fundamental structural elements of the RBC membrane, providing flexibility and resistance to the cell. Proteins, on the other hand, carry out specific membrane functions, such as the transport of molecules and cell-cell recognition.
The RBC membrane contains various types of lipids, including phospholipids, sphingolipids, and cholesterol. The proteins found in the RBC membrane include structural proteins like spectrin and actin, as well as functional proteins such as band-3 and glycophorin.

























