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RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 1
A Seminar as a part of curricular requirement for
M . Pharmacy I year I Semester
Presented by
T. Niranjan Reddy
(20L81S0109)
Department of Pharmacology
Under the guidance of
Dr. P. Ramalingam, MPharm, Ph. D
Research Director and professor of Pharmaceutical and medicinal
chemistry
WESTERN BLOTTING
RIPER
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Contents :
 Introduction
 Types of blotting techniques
 Principle of western blotting
 Procedure for western blotting
 Gel electrophoresis
 Protein transfer
 Antibody probing
 Protein detection
 Analysis and imaging
 Applications
 Limitations
2
RIPER
AUTONOMOUS
NAAC &
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Introduction:
Blotting
 Blotting is a method of transferring proteins, DNA or
RNA, on to a carrier (for example, a nitrocellulose or
PVDF or nylon membrane)
3
RIPER
AUTONOMOUS
NAAC &
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
 Western blotting is a widely used analytical technique in molecular
biology to detect specific protein in a sample of tissue homogenate
or the extract
 It works on the principle of gel electrophoresis
 Proteins are separated based on their size on polyacrylamide gel
Western blotting
RIPER
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NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 6
• Western blotting is an immunoblotting technique which rely on the
specificity of bonding between a molecule of interest and a probe to
allow detection of the molecule of interest in a mixture of many
other similar molecules
• In western blotting, the molecule of interest is a protein and the
probe is typically an antibody raised against that particular protein
• The SDS PAGE (sodium dodecyl sulphate –polyacrylamide gel )
technique is a prerequisite for western blotting.
Principle of western blotting
RIPER
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 7
RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 8
RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 9
• The proteins of the sample are separated by using the gel
electrophoresis
• Electrophoresis is a commonly used method for separating proteins
on the basis of size, shape and charge
• In SDS (sodium dodecyl sulphate) electrophoresis, protein samples
are separated according to their molecular weight.
Gel electrophoresis
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 10
Page protocol
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K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Sample Loading
11
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 12
 On completion of the separation of proteins by polyacrylamide gel
electrophoresis, the next step is to transfer the proteins from the gels to
solid support membrane
 This solid support membrane usually made up of a chemically inert
substance such as nitrocellulose or PVDF (polyvinylidene difluoride)
 The process of transferring proteins from a gel to a membrane while
maintaining their relative positions and resolutions is known as blotting.
protein transfer:
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 13
 After gel electrophoresis it may be necessary to confirm that all the
proteins in the gel have been completely eluted
 As proteins are not directly visible in the gel, the gel must be stained
 Proteins are usually stained with dyes such as Coomassie blue, sliver
stain or deep purple
 After staining a permanent record may be made by imaging the gel
with the suitable instrument.
Protein staining:
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 14
RIPER
AUTONOMOUS
NAAC &
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Blocking :
 The membrane has the ability to bind to proteins in this case
both the target and antibodies are proteins and so there could
be some unwanted binding.
 For meaningful results, the antibodies must bind only to the
protein of interest and not to the membrane
 Non specific binding of antibodies can be reduced by
blocking the unoccupied sites of inert protein or non-ionic
protein
 Blocking agents should possess greater affinity towards
membrane than the antibodies
15
RIPER
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 16
The most commonly used blocking agents are :
 Bovine serum albumin (BSA)
 Non –fat milk
 Casein
 Gelatine
 Dilute solution of tween 20
Blocking agents
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Antibody probing
 After blocking, the blot is incubated with one or more antibodies.
 This uses specific antibody to detect a localize the protein blotted to the
membrane
 The specificity of antigen antibody permits the identification of a single protein
in a complex sample
 The non-labelled primary antibody directed against the target protein and
specific labelled secondary antibody binds to primary antibody
 The secondary antibody is conjugated to an enzyme that is used to indicate the
location of protein
 Secondary antibodies can be a monoclonal or polyclonal antibodies
17
RIPER
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Washing
• The unbound antibodies can cause high background and poor
detection
• Hence, washing the blot removes unbound antibodies from the
membrane
• A dilute solution of tween – 20 in TBS or PBS buffer is
commonly used for washing
18
RIPER
AUTONOMOUS
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Protein detection
• After the unbound probes are washed away, the western
blotting is now ready for detection of probes that are labelled
and bound to the protein of interest
• The marked antibody which is linked to a reporter enzyme
which when exposed to appropriate substrate drives a
colorimetric reaction and produces a colour
• Enzymes such as alkaline phosphatase(AP) and horse radish
peroxidase (HRP) are widely used in detection of proteins
RIPER
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 20
RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 21
 This is the last and major step of the western blotting technique
 Detection of signals using either x-ray film, scanners or a CCD,
results in one or more visible proteins on the membrane image
 The molecular weight of protein can be estimated by comparison
with marker proteins and the amount of protein can be determined
and this is related to band intensity
 Qualitative and quantitative analysis can be done in order to verify
the absence or presence of specific proteins of interest.
Analysis and imaging
RIPER
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NAAC &
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 22
 Analysis of igG fractions purifies from human plasma
 Diagnosis of HIV by ELISA, involves the western blotting technique
 Western blotting technique is also used to detect some forms of
Lyme disease
 Western blotting technique is used in definitive test for BSE, which
is commonly known as mad cow disease
 confirmatory test for hepatitis-B involves western blotting
technique
 This technique are employed in the gene expression studies.
Application of Western Blotting
RIPER
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NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 23
 Very delicate and time consuming process
 If a protein is degraded quickly, then western blotting technique
wont detect it well
 Well trained techniques are required for this technique
 Primary antibody availability is crucial.
Limitations of Western Blotting
RIPER
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K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
References :
• Kurien BT, Scofield RH. 2006. Western blotting. Methods 38: 283–
293.
• Jensen EC. The Basics of Western Blotting. Anat Rec. 2012
Mar 1;295(3):369–71.
• Antharavally BS, et al. A high-affinity reversible protein stain
for Western blots. Analytical biochemistry. 2004;329(2):276–
80
24
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 25

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Western Blotting Technique.

  • 1. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 1 A Seminar as a part of curricular requirement for M . Pharmacy I year I Semester Presented by T. Niranjan Reddy (20L81S0109) Department of Pharmacology Under the guidance of Dr. P. Ramalingam, MPharm, Ph. D Research Director and professor of Pharmaceutical and medicinal chemistry WESTERN BLOTTING
  • 2. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 Contents :  Introduction  Types of blotting techniques  Principle of western blotting  Procedure for western blotting  Gel electrophoresis  Protein transfer  Antibody probing  Protein detection  Analysis and imaging  Applications  Limitations 2
  • 3. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 Introduction: Blotting  Blotting is a method of transferring proteins, DNA or RNA, on to a carrier (for example, a nitrocellulose or PVDF or nylon membrane) 3
  • 4. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
  • 5. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721  Western blotting is a widely used analytical technique in molecular biology to detect specific protein in a sample of tissue homogenate or the extract  It works on the principle of gel electrophoresis  Proteins are separated based on their size on polyacrylamide gel Western blotting
  • 6. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 6 • Western blotting is an immunoblotting technique which rely on the specificity of bonding between a molecule of interest and a probe to allow detection of the molecule of interest in a mixture of many other similar molecules • In western blotting, the molecule of interest is a protein and the probe is typically an antibody raised against that particular protein • The SDS PAGE (sodium dodecyl sulphate –polyacrylamide gel ) technique is a prerequisite for western blotting. Principle of western blotting
  • 7. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 7
  • 8. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 8
  • 9. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 9 • The proteins of the sample are separated by using the gel electrophoresis • Electrophoresis is a commonly used method for separating proteins on the basis of size, shape and charge • In SDS (sodium dodecyl sulphate) electrophoresis, protein samples are separated according to their molecular weight. Gel electrophoresis
  • 10. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 10 Page protocol
  • 11. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 Sample Loading 11
  • 12. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 12  On completion of the separation of proteins by polyacrylamide gel electrophoresis, the next step is to transfer the proteins from the gels to solid support membrane  This solid support membrane usually made up of a chemically inert substance such as nitrocellulose or PVDF (polyvinylidene difluoride)  The process of transferring proteins from a gel to a membrane while maintaining their relative positions and resolutions is known as blotting. protein transfer:
  • 13. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 13  After gel electrophoresis it may be necessary to confirm that all the proteins in the gel have been completely eluted  As proteins are not directly visible in the gel, the gel must be stained  Proteins are usually stained with dyes such as Coomassie blue, sliver stain or deep purple  After staining a permanent record may be made by imaging the gel with the suitable instrument. Protein staining:
  • 14. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 14
  • 15. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 Blocking :  The membrane has the ability to bind to proteins in this case both the target and antibodies are proteins and so there could be some unwanted binding.  For meaningful results, the antibodies must bind only to the protein of interest and not to the membrane  Non specific binding of antibodies can be reduced by blocking the unoccupied sites of inert protein or non-ionic protein  Blocking agents should possess greater affinity towards membrane than the antibodies 15
  • 16. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 16 The most commonly used blocking agents are :  Bovine serum albumin (BSA)  Non –fat milk  Casein  Gelatine  Dilute solution of tween 20 Blocking agents
  • 17. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 Antibody probing  After blocking, the blot is incubated with one or more antibodies.  This uses specific antibody to detect a localize the protein blotted to the membrane  The specificity of antigen antibody permits the identification of a single protein in a complex sample  The non-labelled primary antibody directed against the target protein and specific labelled secondary antibody binds to primary antibody  The secondary antibody is conjugated to an enzyme that is used to indicate the location of protein  Secondary antibodies can be a monoclonal or polyclonal antibodies 17
  • 18. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 Washing • The unbound antibodies can cause high background and poor detection • Hence, washing the blot removes unbound antibodies from the membrane • A dilute solution of tween – 20 in TBS or PBS buffer is commonly used for washing 18
  • 19. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 Protein detection • After the unbound probes are washed away, the western blotting is now ready for detection of probes that are labelled and bound to the protein of interest • The marked antibody which is linked to a reporter enzyme which when exposed to appropriate substrate drives a colorimetric reaction and produces a colour • Enzymes such as alkaline phosphatase(AP) and horse radish peroxidase (HRP) are widely used in detection of proteins
  • 20. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 20
  • 21. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 21  This is the last and major step of the western blotting technique  Detection of signals using either x-ray film, scanners or a CCD, results in one or more visible proteins on the membrane image  The molecular weight of protein can be estimated by comparison with marker proteins and the amount of protein can be determined and this is related to band intensity  Qualitative and quantitative analysis can be done in order to verify the absence or presence of specific proteins of interest. Analysis and imaging
  • 22. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 22  Analysis of igG fractions purifies from human plasma  Diagnosis of HIV by ELISA, involves the western blotting technique  Western blotting technique is also used to detect some forms of Lyme disease  Western blotting technique is used in definitive test for BSE, which is commonly known as mad cow disease  confirmatory test for hepatitis-B involves western blotting technique  This technique are employed in the gene expression studies. Application of Western Blotting
  • 23. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 23  Very delicate and time consuming process  If a protein is degraded quickly, then western blotting technique wont detect it well  Well trained techniques are required for this technique  Primary antibody availability is crucial. Limitations of Western Blotting
  • 24. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 References : • Kurien BT, Scofield RH. 2006. Western blotting. Methods 38: 283– 293. • Jensen EC. The Basics of Western Blotting. Anat Rec. 2012 Mar 1;295(3):369–71. • Antharavally BS, et al. A high-affinity reversible protein stain for Western blots. Analytical biochemistry. 2004;329(2):276– 80 24
  • 25. RIPER AUTONOMOUS NAAC & NBA (UG) SIRO- DSIR Raghavendra Institute of Pharmaceutical Education and Research - Autonomous K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 25