Protein microarray.pptx

PROTEIN MICROARRAY
DR.MUMTAZ ALI NAREJO
PhD SCHOLAR , SALU KHAIRPUR
OUTLINES
• Introduction
• History
• Preparation
• Methods
• Types
• Detection
• Applications
• Challanges
INTRODUCTION
• a high-throughput method used to track the
interactions and activities of proteins, and to
determine their function, and determining
function on a large scale
• large numbers of proteins can be tracked in
parallel
• The chip consists of a support surface such as a
glass slide, nitrocellulose membrane, bead,
or microtitre plate, to which an array of capture
proteins is bound
• Probe molecules, typically labeled with a
fluorescent dye, are added to the array
• Any reaction between the probe and the
immobilised protein emits a fluorescent signal
that is read by a laser scanner
• rapid, automated, economical, and highly
sensitive, consuming small quantities of
samples and reagents
HISTORY
• antibody microarrays / antibody matrix
• 1983 : Roger Ekins
• DNA microarrays
• Limitations : gene expression
• mRNA don’t express proteins
• protein : functional role in cell response
• post-translational modifications :protein function,
are not visible on DNA microarrays
• 2D gel electrophoresis or chromatography
PREPARATION OF PROTEIN ARRAY
• microscope slides, membranes, beads or microtitre plates
• Support : protein => immobilized
• binding ability is retained
• Microscope : glass or silicon
• Nitrocellulose : highest protein binding
• solid surface => coating
 immobilising the protein
 preventing its denaturation
 orienting it in the appropriate direction
 binding sites are accessible
 providing a hydrophilic environment
• Immobilising agents
 aluminium or gold
 hydrophilic polymers
 polyacrylamide gels
 treatment with amines, aldehyde or epoxy
• Coatings
 physical vapour deposition (PVD)
 chemical vapour deposition (CVD)
• aqueous environment /buffers
 high percent of glycerol (to lower the freezing point)
 humidity of the manufacturing environment
METHODS
• robots/robotic contact printingrobot/potting
• ink-jetting
• Piezoelectric spotting
• Photolithography
TYPES
• Analytical microarrays/capture arrays
• Functional protein microarrays : target protein
arrays
• Reverse phase protein microarray
Protein microarray.pptx
DETECTION
DETECTION
APPLICATIONS
• Diagnostics
detection of antigens and antibodies
profiling of sera to discover new
disease biomarkers
monitoring of disease states
responses to therapy
monitoring of environment and food
Digital bioassay
• Proteomics
protein expression profiling
Protein microarray.pptx
Protein microarray.pptx
• protein functional analysis
identification of protein–protein interactions
protein–phospholipid interactions
small molecule targets
enzymatic substrates
receptor ligands
• antibody characterization
cross-reactivity
Specificity
mapping epitopes
• treatment development
antigen-specific therapies for autoimmunity,
cancer and allergies
CHALLANGES
• quite difficult to handle
• Requires more steps than DNA
• Surface & method of attachment
• Producing of array with long shelf life
• Quantifying level of bound protein
• extracting the detected protein from the chip
• reducing non-specific binding by the capture
agents
• capacity of the chip
THANKYOU
Protein microarray.pptx
Protein microarray.pptx
Protein microarray.pptx
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Protein microarray.pptx

  • 1. PROTEIN MICROARRAY DR.MUMTAZ ALI NAREJO PhD SCHOLAR , SALU KHAIRPUR
  • 2. OUTLINES • Introduction • History • Preparation • Methods • Types • Detection • Applications • Challanges
  • 3. INTRODUCTION • a high-throughput method used to track the interactions and activities of proteins, and to determine their function, and determining function on a large scale • large numbers of proteins can be tracked in parallel • The chip consists of a support surface such as a glass slide, nitrocellulose membrane, bead, or microtitre plate, to which an array of capture proteins is bound
  • 4. • Probe molecules, typically labeled with a fluorescent dye, are added to the array • Any reaction between the probe and the immobilised protein emits a fluorescent signal that is read by a laser scanner • rapid, automated, economical, and highly sensitive, consuming small quantities of samples and reagents
  • 5. HISTORY • antibody microarrays / antibody matrix • 1983 : Roger Ekins • DNA microarrays • Limitations : gene expression • mRNA don’t express proteins • protein : functional role in cell response • post-translational modifications :protein function, are not visible on DNA microarrays • 2D gel electrophoresis or chromatography
  • 6. PREPARATION OF PROTEIN ARRAY • microscope slides, membranes, beads or microtitre plates • Support : protein => immobilized • binding ability is retained • Microscope : glass or silicon • Nitrocellulose : highest protein binding • solid surface => coating  immobilising the protein  preventing its denaturation  orienting it in the appropriate direction  binding sites are accessible  providing a hydrophilic environment
  • 7. • Immobilising agents  aluminium or gold  hydrophilic polymers  polyacrylamide gels  treatment with amines, aldehyde or epoxy • Coatings  physical vapour deposition (PVD)  chemical vapour deposition (CVD) • aqueous environment /buffers  high percent of glycerol (to lower the freezing point)  humidity of the manufacturing environment
  • 8. METHODS • robots/robotic contact printingrobot/potting • ink-jetting • Piezoelectric spotting • Photolithography
  • 9. TYPES • Analytical microarrays/capture arrays • Functional protein microarrays : target protein arrays • Reverse phase protein microarray
  • 13. APPLICATIONS • Diagnostics detection of antigens and antibodies profiling of sera to discover new disease biomarkers monitoring of disease states responses to therapy monitoring of environment and food Digital bioassay • Proteomics protein expression profiling
  • 16. • protein functional analysis identification of protein–protein interactions protein–phospholipid interactions small molecule targets enzymatic substrates receptor ligands • antibody characterization cross-reactivity Specificity mapping epitopes • treatment development antigen-specific therapies for autoimmunity, cancer and allergies
  • 17. CHALLANGES • quite difficult to handle • Requires more steps than DNA • Surface & method of attachment • Producing of array with long shelf life • Quantifying level of bound protein • extracting the detected protein from the chip • reducing non-specific binding by the capture agents • capacity of the chip