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STRUCTURE & FUNCTION OF
PLASMA MEMBRANE
PLASMA MEMBRANE
• The membrane enclosing a cell is called cell membrane or plasma membrane (animal cells) and plasma lemma
(plant cells).
• It contains proteins and lipids in the ratio of 80 : 20 in bacteria on one extreme and on the other extreme 20 : 80
in some nerve cells.
• The over all composition of most of the cell membranes is 40-50% protein and 50-60% lipids; both the
components vary in their composition.
• They have been further classified into different types. The proportion of these lipids varies in different
membranes. For example, plasma membrane is composed of 55% phospholipids. 5% glycolipids, 20% steroids
and 20% other lipids.
• But endoplasmic reticulum contains 65% phospholipids, 30% glycolipids and 5% steroids. The percentage of
these lipid types in mitochondrial membranes is 75% (phospholipids), 20% (glycolipids) and 5% (steroids).
• Bacterial membrane constrains a high proportion of cholesterol (70%) and a lesser proportion of phospholipids
(30%). The different types of phospholipids found in the biological membranes.
MEMBRANE LIPIDS
Phospholipids
Phosphoglycerides
 Phosphotidylcholine
 Phosphodidylethanolamine
 Phosphotidylserine
 Phosphotidylthreonine
 Phosphotidylglycerol
 Phosphotidylinositol
 Diphosphotidyl glycerol
Sphingo-phhospholipids
 Sphingomyelin
Glycolipids
 Cerebrosides
 Sulfatides
 Gangliosides
Steroids
Cholesterol
Stigmasterol
STRUCTURE OF PLASMA MEMBRANE
• Electron microscopic studies have revealed that the 7-8 nm thick plasma membrane has two electron
dense regions separated by an electron light central region.
• These three layers together are called “trilaminar”.
• Robertson termed them as “unit membrane”; he proposed the “unit membrane
hypothesis” according to which all the biological membranes have “trilaminar” organisation.
• The most widely accepted model of plasma membrane is the “fluid mosaic model” which was
proposed by Singer and Nicholson in 1972.
• According to this model, Two monolayers of lipid molecules form a lipid bilayer.
Lipid Bilayer:
• The lipid bilayer is made up of two lipid layers, each layer being one molecule thick. This organisation is common
to all biological membranes, but there are notable differences in the particular kinds of lipids present.
• Each lipid molecule has a ‘hydrophilic’ head and one or two ‘hydrophobic’ tails, making
them “amphipathic” molecules.
• The hydrophilic ends of the lipid molecules are oriented toward the outside of the membrane of the cell, while
their hydrophobic tails are oriented inward, the latter constitute the interior hydrophobic region of the
membrane.
• The tails of the lipid molecules are made up of fatty acids, both saturated and unsaturated fatty acids may be
present.
• In myelin membrane, unsaturated fatty acids constitute less than 10%, while in the mitochondrial and chloroplast
membranes, unsaturated fatty acids make up more than 50% of the fatly acids.
• Tails of saturated fatty acids extend freely but those of the unsaturated chain bend at the double bond.
Membrane Proteins:
• In general, the ratio of lipids and proteins is equal (about 50% each) in the biological membranes but the
organellar membranes contain a high proportion (75-80%) of proteins.
• Integral proteins are embedded within the lipid bilayer, and they can move laterally within the bilayer.
• The region (domain) of the protein molecule lying within the lipid bilayer is “hydrophobic” while that lying out
side the bilayer is “hydrophilic”.
• The protein molecules that pass through the lipid bilayer and are exposed on both the sides of the lipid bilayer
are called trans-membrane.
• Trans-membrane proteins have one or more regions containing 21-26 hydrophobic amino acids which are coiled
into an α-helix.
The membrane proteins are of different kinds within the membrane:
• Proteins with single membrane-spanning region (hydrophobic region)
 Group I Proteins - Group I proteins are those whose N-terminal end is exposed to the exterior of the cell,
while the C-terminal end is exposed in the cytoplasm.
 Group II Proteins - Such proteins have their C-terminal end exposed to the exterior of the cell, while their N-
terminal end is exposed into the cytoplasm. Such proteins are less common.
 Proteins with ‘odd’ number of hydrophobic regions: In such proteins, the N-terminal and C-terminal regions lie
on different sides of the membrane.
 Proteins with ‘even’ number of hydrophobic regions: These proteins have both, their N-terminal and C-terminal
ends on the same side of the lipid bilayer.
• Proteins with multiple membrane-spanning regions.
• Lipids are synthesized in the ER, and are transported to the cytoplasmic surface of the membrane, from where
they are transported to the outer monolayer of the lipid bilayer.
• The protein involved in this movement is called flippase.
Carbohydrates - Glycoproteins:
• The outer surface of the membrane is rich in carbohydrate groups such as, glycoproteins or glycolipids.
• The inner surface (cytoplasmic surface), on the other hand, is charged negatively (-) due to the
predominance of unsaturated fatty acid chains in the lipid molecules forming the inner monolayer.
• Thus there is an asymmetry in the organisation of the lipid bilayer of the plasma membrane.
• One important property of the plasma membrane is that it can produce “vesicles” by a process of
budding.
• The vesicles can fuse with the membrane by the reverse process.
FLUID MOSAIC
MODEL OF
PLASMA MEMBRANE
• Singer and Nicolson (1972) have given the fluid mosaic model of
plasma membrane to explain its major features.
• This model is well accepted. According to this model, the plasma
membrane is quasi-fluid structure in which lipids and proteins
are arranged in a mosaic manner.
• The globular proteins are of two types: Extrinsic (peripheral)
proteins and Intrinsic (integral) proteins.
• The extrinsic protein is soluble and, therefore, dissociates from
the membrane, while the intrinsic protein is insoluble and could
not (or rarely) dissociate.
• The intrinsic proteins are partially embedded either on outer
surface or on inner surface of the bilayer and take part in lateral
diffusion in lipid bilayer.
• The lipid matrix of membrane has fluidity that permits the
membrane components to move laterally.
• The membrane fluidity is due to the hydrophobic interactions of
lipids and proteins.
• The fluidity is important for a number of membrane functions.
Phospholipids and many intrinsic proteins are amphipathic i.e.
they possess both hydrophilic and hydrophobic groups.
• Phospholipids are the complex lipids which are made up of
glycerol, two fatty acids and, in place of a third fatty acid, a
phosphate group bounded to one of several organic groups.
• They have polar (hydrophilic) as well as non-polar (hydrophobic)
regions.
• Polar portion consists of a phosphate group and glycerol, while
non-polar portion consists of fatty acids.
• All non-polar parts of phospholipid make contact only with the
non-polar portion of the neighbouring molecules.
• The polar portion occurs towards outside. This characteristic fea-
ture gives the appearance of bilayer.
• However, between the fatty acid chains proper spacing is maintained by interspersing unsaturated chains
throughout the membrane.
• This type of arrangement maintains the semi-fluidity of plasma membrane.
• The presence of complex lipids becomes a key character of certain microorganisms on the basis of which they
can be identified.
• For example, the cell wall of Mycobacterium contains high amount of lipids such as waxes and glycolipids which
gives the bacterium a distinctive staining characteristic.
• In some microorganisms such as mycoplasmas and fungi, sterols are found to be associated within the plasma
membrane.
• Sterols are structurally different from the lipids. The -OH group in cholesterol makes it a sterol. Sterols are
alcohols composed of hydrocarbon rings attached to hydrocarbon chain.
• The sterols separate the fatty acid chains and check packing which harden the plasma membrane at low
temperature.
• In case of certain bacteria hopanoids are present which have similar role to that of sterols found in certain fungi.
FUNCTION OF PLASMA MEMBRANE
A PHYSICAL BARRIER
• The plasma membrane surrounds all cells and physically separates the cytoplasm, which is the material
that makes up the cell, from the extracellular fluid outside the cell.
• This protects all the components of the cell from the outside environment and allows separate
activities to occur inside and outside the cell.
• The plasma membrane provides structural support to the cell. It tethers the cytoskeleton, which is a
network of protein filaments inside the cell that hold all the parts of the cell in place.
• This gives the cell its shape and it provides additional support to the cell. Certain organisms such as
plants and fungi have a cell wall in addition to the membrane. The cell wall is composed of molecules
such as cellulose.
MOVEMENT OF MATERIALS
Simple Diffusion:
• Simple diffusion refers to the unaided movement of a substance
from the region of its higher concentration to a region of its
lower concentration till an equilibrium is achieved.
• The plasma membrane is called a selectively permeable or
differentially permeable membrane.
• When water molecules move through a differentially permeable
membrane from lower to higher concentration of solutes, the
process is called osmosis.
Facilitated Diffusion:
• It is similar to simple diffusion but the rate of the solute
movement increases by interaction with specific membrane
transporters. The transporters are “trans membrane proteins.”
Active Transport:
• It is the mechanism by which movement of solutes occurs in one
direction (unidirectional), i.e., from lower to higher concentration.
• This is an energy requiring process. The energy is obtained from
hydrolysis of ATP and from other sources.
Endocytosis & Exocytosis:
• Endocytosis is the process of capturing a substance or particle from
outside the cell by engulfing it with the cell membrane.
• The membrane folds over the substance and it becomes completely
enclosed by the membrane.
Phagocytosis or cellular eating, occurs when the dissolved materials enter the
cell. The plasma membrane engulfs the solid material, forming a phagocytic
vesicle.
Pinocytosis or cellular drinking, occurs when the plasma membrane folds
inward to form a channel allowing dissolved substances to enter the cell.
When the channel is closed, the liquid is encircled within a pinocytic vesicle.
• Exocytosis describes the process of vesicles fusing with the plasma
membrane and releasing their contents to the outside of the cell.
• Exocytosis occurs when a cell produces substances for export, such as
a protein, or when the cell is getting rid of a waste product or a toxin.
• Newly made membrane proteins and membrane lipids are
moved on top the plasma membrane by exocytosis.
There from outside into the cell:
(i) Through Channels - The channels are made by trans membrane
proteins. Ions are transferred by this process. Separate channels exist for
K+, Na+, and Ca2+ etc.
(ii) By Receptor Itself - The ligand, such as sugars, binds to the receptor
and is transported from extracellular side to the cytoplasm side of the
membrane.
(iii) Receptor Internalization - The ligand binds to receptor which
triggers the process of internalization. Vesicle is formed by endocytosis
and the ligand is brought into the cell.
Metabolic Functions:
• Plasma membrane plays an important role in metabolism. Several enzymes
are located on the cell surface, such as, those involved in extracellular nutrient
breakdown and those involved in cell wall biosynthesis.
• In prokaryotes, respiratory enzymes are located in the plasma membrane.
Communication Recognition and Adhesion:
• Some important functions of the plasma membrane are the communication
between cells, recognition and cell to cell adhesion.
• Such functions are carried out by “receptors” which are trans membrane
proteins or integral proteins.
• The extracellular substance, called “ligand” binds to the specific receptors.
• This binding triggers a change in the function of the membrane. It can
transduce signal in the cytoplasm, the phenomenon is called “signal
transduction”.
There are two types of signal transduction:
• When a ligand binds to the receptor (a trans membrane protein), it activates the kinase activity of the cytoplasmic
domain of the receptor leading to its phosphorylation. The phosphorylated receptor associates with the target
protein in the cytoplasm.
• The ligand receptor binding may activate the G protein associated with the plasma membrane. G proteins are
guanine nucleotide-binding trimeric proteins consisting of the subunits α (monomer) and βγ (dimer). G protein is
inactive when the trimer (αβγ) is bound to GDP.
o On activation, GDP (bound to the a subunit) is replaced by GTP and the G protein dissociates into the subunits
α, β and γ dimer.
o Then one of the active subunits (either α or βγ) acts upon the target proteins in the cytoplasm. It either activates
or represses the target proteins.
• Different cells may have different receptors, and therefore, they may respond to different signals.
• Formation of tissues and organs in multicellular organisms occurs when cells adhere to each other in specific
ways.
• Glycoproteins are known to be involved in cell-to-cell recognition and adhesion. Membrane junctions are
formed in animal cells for different functions.
• “Tight junctions” prevent the movement of molecules through the spaces between adjacent cells.
• Desmosomes (specialized areas of cell surface that serve to bind the surface to another structure) provide
mechanical strength to hold the cells together in conditions when tissues are exposed to forces that lead to
stretching.
• “Gap junctions” occur in both, vertebrates and invertebrates, especially in tissues which require quick
communication between cells, e.g., nerve cells, muscles etc.
• They enable small molecules to move from one cell to the other.
• One type of receptor may respond to protein hormones, some other type of receptor respond to neuro
transmitters (e.g., acetylcholine), while another type of receptors respond to antigens etc.

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Plasma membrane.pptx

  • 1. STRUCTURE & FUNCTION OF PLASMA MEMBRANE
  • 2. PLASMA MEMBRANE • The membrane enclosing a cell is called cell membrane or plasma membrane (animal cells) and plasma lemma (plant cells). • It contains proteins and lipids in the ratio of 80 : 20 in bacteria on one extreme and on the other extreme 20 : 80 in some nerve cells. • The over all composition of most of the cell membranes is 40-50% protein and 50-60% lipids; both the components vary in their composition. • They have been further classified into different types. The proportion of these lipids varies in different membranes. For example, plasma membrane is composed of 55% phospholipids. 5% glycolipids, 20% steroids and 20% other lipids. • But endoplasmic reticulum contains 65% phospholipids, 30% glycolipids and 5% steroids. The percentage of these lipid types in mitochondrial membranes is 75% (phospholipids), 20% (glycolipids) and 5% (steroids). • Bacterial membrane constrains a high proportion of cholesterol (70%) and a lesser proportion of phospholipids (30%). The different types of phospholipids found in the biological membranes.
  • 3. MEMBRANE LIPIDS Phospholipids Phosphoglycerides  Phosphotidylcholine  Phosphodidylethanolamine  Phosphotidylserine  Phosphotidylthreonine  Phosphotidylglycerol  Phosphotidylinositol  Diphosphotidyl glycerol Sphingo-phhospholipids  Sphingomyelin Glycolipids  Cerebrosides  Sulfatides  Gangliosides Steroids Cholesterol Stigmasterol
  • 4. STRUCTURE OF PLASMA MEMBRANE • Electron microscopic studies have revealed that the 7-8 nm thick plasma membrane has two electron dense regions separated by an electron light central region. • These three layers together are called “trilaminar”. • Robertson termed them as “unit membrane”; he proposed the “unit membrane hypothesis” according to which all the biological membranes have “trilaminar” organisation. • The most widely accepted model of plasma membrane is the “fluid mosaic model” which was proposed by Singer and Nicholson in 1972. • According to this model, Two monolayers of lipid molecules form a lipid bilayer.
  • 5. Lipid Bilayer: • The lipid bilayer is made up of two lipid layers, each layer being one molecule thick. This organisation is common to all biological membranes, but there are notable differences in the particular kinds of lipids present. • Each lipid molecule has a ‘hydrophilic’ head and one or two ‘hydrophobic’ tails, making them “amphipathic” molecules. • The hydrophilic ends of the lipid molecules are oriented toward the outside of the membrane of the cell, while their hydrophobic tails are oriented inward, the latter constitute the interior hydrophobic region of the membrane. • The tails of the lipid molecules are made up of fatty acids, both saturated and unsaturated fatty acids may be present. • In myelin membrane, unsaturated fatty acids constitute less than 10%, while in the mitochondrial and chloroplast membranes, unsaturated fatty acids make up more than 50% of the fatly acids. • Tails of saturated fatty acids extend freely but those of the unsaturated chain bend at the double bond.
  • 6. Membrane Proteins: • In general, the ratio of lipids and proteins is equal (about 50% each) in the biological membranes but the organellar membranes contain a high proportion (75-80%) of proteins. • Integral proteins are embedded within the lipid bilayer, and they can move laterally within the bilayer. • The region (domain) of the protein molecule lying within the lipid bilayer is “hydrophobic” while that lying out side the bilayer is “hydrophilic”. • The protein molecules that pass through the lipid bilayer and are exposed on both the sides of the lipid bilayer are called trans-membrane. • Trans-membrane proteins have one or more regions containing 21-26 hydrophobic amino acids which are coiled into an α-helix. The membrane proteins are of different kinds within the membrane:
  • 7. • Proteins with single membrane-spanning region (hydrophobic region)  Group I Proteins - Group I proteins are those whose N-terminal end is exposed to the exterior of the cell, while the C-terminal end is exposed in the cytoplasm.  Group II Proteins - Such proteins have their C-terminal end exposed to the exterior of the cell, while their N- terminal end is exposed into the cytoplasm. Such proteins are less common.  Proteins with ‘odd’ number of hydrophobic regions: In such proteins, the N-terminal and C-terminal regions lie on different sides of the membrane.  Proteins with ‘even’ number of hydrophobic regions: These proteins have both, their N-terminal and C-terminal ends on the same side of the lipid bilayer. • Proteins with multiple membrane-spanning regions. • Lipids are synthesized in the ER, and are transported to the cytoplasmic surface of the membrane, from where they are transported to the outer monolayer of the lipid bilayer. • The protein involved in this movement is called flippase.
  • 8. Carbohydrates - Glycoproteins: • The outer surface of the membrane is rich in carbohydrate groups such as, glycoproteins or glycolipids. • The inner surface (cytoplasmic surface), on the other hand, is charged negatively (-) due to the predominance of unsaturated fatty acid chains in the lipid molecules forming the inner monolayer. • Thus there is an asymmetry in the organisation of the lipid bilayer of the plasma membrane. • One important property of the plasma membrane is that it can produce “vesicles” by a process of budding. • The vesicles can fuse with the membrane by the reverse process.
  • 9. FLUID MOSAIC MODEL OF PLASMA MEMBRANE • Singer and Nicolson (1972) have given the fluid mosaic model of plasma membrane to explain its major features. • This model is well accepted. According to this model, the plasma membrane is quasi-fluid structure in which lipids and proteins are arranged in a mosaic manner. • The globular proteins are of two types: Extrinsic (peripheral) proteins and Intrinsic (integral) proteins. • The extrinsic protein is soluble and, therefore, dissociates from the membrane, while the intrinsic protein is insoluble and could not (or rarely) dissociate. • The intrinsic proteins are partially embedded either on outer surface or on inner surface of the bilayer and take part in lateral diffusion in lipid bilayer. • The lipid matrix of membrane has fluidity that permits the membrane components to move laterally. • The membrane fluidity is due to the hydrophobic interactions of lipids and proteins.
  • 10. • The fluidity is important for a number of membrane functions. Phospholipids and many intrinsic proteins are amphipathic i.e. they possess both hydrophilic and hydrophobic groups. • Phospholipids are the complex lipids which are made up of glycerol, two fatty acids and, in place of a third fatty acid, a phosphate group bounded to one of several organic groups. • They have polar (hydrophilic) as well as non-polar (hydrophobic) regions. • Polar portion consists of a phosphate group and glycerol, while non-polar portion consists of fatty acids. • All non-polar parts of phospholipid make contact only with the non-polar portion of the neighbouring molecules. • The polar portion occurs towards outside. This characteristic fea- ture gives the appearance of bilayer.
  • 11. • However, between the fatty acid chains proper spacing is maintained by interspersing unsaturated chains throughout the membrane. • This type of arrangement maintains the semi-fluidity of plasma membrane. • The presence of complex lipids becomes a key character of certain microorganisms on the basis of which they can be identified. • For example, the cell wall of Mycobacterium contains high amount of lipids such as waxes and glycolipids which gives the bacterium a distinctive staining characteristic. • In some microorganisms such as mycoplasmas and fungi, sterols are found to be associated within the plasma membrane. • Sterols are structurally different from the lipids. The -OH group in cholesterol makes it a sterol. Sterols are alcohols composed of hydrocarbon rings attached to hydrocarbon chain. • The sterols separate the fatty acid chains and check packing which harden the plasma membrane at low temperature. • In case of certain bacteria hopanoids are present which have similar role to that of sterols found in certain fungi.
  • 12. FUNCTION OF PLASMA MEMBRANE
  • 13. A PHYSICAL BARRIER • The plasma membrane surrounds all cells and physically separates the cytoplasm, which is the material that makes up the cell, from the extracellular fluid outside the cell. • This protects all the components of the cell from the outside environment and allows separate activities to occur inside and outside the cell. • The plasma membrane provides structural support to the cell. It tethers the cytoskeleton, which is a network of protein filaments inside the cell that hold all the parts of the cell in place. • This gives the cell its shape and it provides additional support to the cell. Certain organisms such as plants and fungi have a cell wall in addition to the membrane. The cell wall is composed of molecules such as cellulose.
  • 14. MOVEMENT OF MATERIALS Simple Diffusion: • Simple diffusion refers to the unaided movement of a substance from the region of its higher concentration to a region of its lower concentration till an equilibrium is achieved. • The plasma membrane is called a selectively permeable or differentially permeable membrane. • When water molecules move through a differentially permeable membrane from lower to higher concentration of solutes, the process is called osmosis. Facilitated Diffusion: • It is similar to simple diffusion but the rate of the solute movement increases by interaction with specific membrane transporters. The transporters are “trans membrane proteins.”
  • 15. Active Transport: • It is the mechanism by which movement of solutes occurs in one direction (unidirectional), i.e., from lower to higher concentration. • This is an energy requiring process. The energy is obtained from hydrolysis of ATP and from other sources. Endocytosis & Exocytosis: • Endocytosis is the process of capturing a substance or particle from outside the cell by engulfing it with the cell membrane. • The membrane folds over the substance and it becomes completely enclosed by the membrane. Phagocytosis or cellular eating, occurs when the dissolved materials enter the cell. The plasma membrane engulfs the solid material, forming a phagocytic vesicle. Pinocytosis or cellular drinking, occurs when the plasma membrane folds inward to form a channel allowing dissolved substances to enter the cell. When the channel is closed, the liquid is encircled within a pinocytic vesicle.
  • 16. • Exocytosis describes the process of vesicles fusing with the plasma membrane and releasing their contents to the outside of the cell. • Exocytosis occurs when a cell produces substances for export, such as a protein, or when the cell is getting rid of a waste product or a toxin. • Newly made membrane proteins and membrane lipids are moved on top the plasma membrane by exocytosis. There from outside into the cell: (i) Through Channels - The channels are made by trans membrane proteins. Ions are transferred by this process. Separate channels exist for K+, Na+, and Ca2+ etc. (ii) By Receptor Itself - The ligand, such as sugars, binds to the receptor and is transported from extracellular side to the cytoplasm side of the membrane. (iii) Receptor Internalization - The ligand binds to receptor which triggers the process of internalization. Vesicle is formed by endocytosis and the ligand is brought into the cell.
  • 17. Metabolic Functions: • Plasma membrane plays an important role in metabolism. Several enzymes are located on the cell surface, such as, those involved in extracellular nutrient breakdown and those involved in cell wall biosynthesis. • In prokaryotes, respiratory enzymes are located in the plasma membrane. Communication Recognition and Adhesion: • Some important functions of the plasma membrane are the communication between cells, recognition and cell to cell adhesion. • Such functions are carried out by “receptors” which are trans membrane proteins or integral proteins. • The extracellular substance, called “ligand” binds to the specific receptors. • This binding triggers a change in the function of the membrane. It can transduce signal in the cytoplasm, the phenomenon is called “signal transduction”.
  • 18. There are two types of signal transduction: • When a ligand binds to the receptor (a trans membrane protein), it activates the kinase activity of the cytoplasmic domain of the receptor leading to its phosphorylation. The phosphorylated receptor associates with the target protein in the cytoplasm. • The ligand receptor binding may activate the G protein associated with the plasma membrane. G proteins are guanine nucleotide-binding trimeric proteins consisting of the subunits α (monomer) and βγ (dimer). G protein is inactive when the trimer (αβγ) is bound to GDP. o On activation, GDP (bound to the a subunit) is replaced by GTP and the G protein dissociates into the subunits α, β and γ dimer. o Then one of the active subunits (either α or βγ) acts upon the target proteins in the cytoplasm. It either activates or represses the target proteins.
  • 19. • Different cells may have different receptors, and therefore, they may respond to different signals. • Formation of tissues and organs in multicellular organisms occurs when cells adhere to each other in specific ways. • Glycoproteins are known to be involved in cell-to-cell recognition and adhesion. Membrane junctions are formed in animal cells for different functions. • “Tight junctions” prevent the movement of molecules through the spaces between adjacent cells. • Desmosomes (specialized areas of cell surface that serve to bind the surface to another structure) provide mechanical strength to hold the cells together in conditions when tissues are exposed to forces that lead to stretching. • “Gap junctions” occur in both, vertebrates and invertebrates, especially in tissues which require quick communication between cells, e.g., nerve cells, muscles etc. • They enable small molecules to move from one cell to the other. • One type of receptor may respond to protein hormones, some other type of receptor respond to neuro transmitters (e.g., acetylcholine), while another type of receptors respond to antigens etc.