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Department of Pharmacology
MPL 104 T – CMP
Unit - IV 03-05-2021
What is proteomics?
Proteomics is the analysis of the
protein complement to the genome
Genomics Proteomics
Gene Transcript Protein
Proteomics is multidisciplinary
Proteomics
Molecular
Biology
Biology
Analytical
Chemistry
Protein
Biochemistry
Bioinformatics
Proteomics Research
•Basic research:
To understand the molecular mechanisms
underlying life.
•Applied research:
Clinical testing for proteins associated with
pathological states (e.g. cancer).
Applications of Proteomics
Proteomics
Structural
Proteomics
Proteome
Mining
Post-
translational
Modifications
Protein
Expression
Profiling
Functional
Proteomics
Protein-
protein
Interactions
Glycoyslation
Phosphorylation
Proteolysis
Yeast two-hybrid
Co-precipitation
Phage Display
Drug Discovery
Target ID
Differential Display
Yeast Genomics
Affinity Purified
Protein Complexes
Mouse Knockouts
Medical
Microbiology
Signal
Transduction
Disease
Mechanisms
Organelle
Composition
Subproteome
Isolation
Protein
Complexes
For example: Hemoglobin
Picks up oxygen in the lungs, travels through
the blood, and delivers it to the cells.
O2
hemoglobin
Hbβ Hbα
Hbβ
Hbα
ATG GTG CAC CTG ACT CCT GAG GAG … ATG GTG CAC CTG ACT CCT GTG GAG …
E
E
M V H L T P … E
V
M V H L T P …
Normal Hbβ Mutated Hbβ
Sickle cell disease is caused
by a single amino acid change.
Summary – what is proteomics?
•Involves the study of proteins
•Proteomics is multidisciplinary
•Proteomics is being applied to both basic and clinical
research
Why study proteins?
What are PROTEINS?
Proteins are large, complex molecules
that serve diverse functional and
structural roles within cells.
Transport
Hemoglobin
Carries O2
Defense
Antibody
Fights Viruses
Enzyme
Protease
Degrades Protein
Support
Keratin
Forms Hair and
Nails
Motion
Actin
Contracts Muscles
Regulation
Insulin
Controls Blood Glucose
Proteins do most of the work
in the cell
Proteins are comprised of amino
acid building blocks
R
O
OH
C
N H
H
Acid
Base
Variable
CH
+
H2O
Dipeptide
Peptide Bond
Amino acid 1 Amino acid 2
R1
O
C
C
N O
H
H2 H
R2
H
C
C
N O
O
H
H H
R1
O
C
C
R2
O
C C
H
H
N
H2
N
H OH
Summary – why study proteins?
•Biological workhorses that carry out most of the
functions within the cell
•Serve diverse functional and structural roles
•Composed of amino acids that are covalently
linked by peptide bonds
•Synthesized during the translation process
•Must fold correctly to perform their functions
Proteomic tools and methods
Proteomic tools to study proteins
• Protein isolation
• Protein separation
• Protein identification
Protein Isolation
How are proteins isolated?
• Mechanical Methods
– grinding – break open cell
– centrifugation – remove insoluble debris
• Chemical Methods
– detergent – breaks open cell compartments
– reducing agent – breaks specific protein
bonds
– heat – break peptide bonds to “linearize”
protein
Protein isolation procedure
Find a sample
Pick it
Grind sample in buffer
Transfer to tube
Heat the sample
Centrifuge to remove
insoluble material
“pure” protein
solution
Recover supernatant Keep solution for gel analysis
Protein X
“pure” protein
solution
Isolated Protein X
Summary – protein isolation
•Proteins can be isolated from a variety of samples
•Proteomics includes the use of both mechanical and
chemical methods to isolate proteins
•Opening cell or cellular compartments
•Breaking bonds and “linearizing” proteins
•Removal cell debris
Protein Separation
SDS-PAGE
Why separate proteins?
“PURE” Protein Solution
Tube 1
Decreased Protein ID
Increased Complexity
Tube 2
Increased Protein ID
Decreased Complexity
How to separate proteins?
Separating intact proteins is to take
advantage of their diversity in
physical properties, especially
isoelectric point and molecular weight
Methods of Protein Separation
• Sodium Dodecyl Sulfate –
Polyacrylamide Gel Electrophoresis
(SDS-PAGE)
• Isoelectric Focusing (IEF)
SDS-PolyAcrylamide Gel
Electrophoresis (SDS-PAGE) is a
widely used technique to separate
proteins in solution
SDS-PAGE separates only by
molecular weight
• Molecular weight is mass one molecule
• Dalton (Da) is a small unit of mass
used to express atomic and molecular
masses.
PAGE is widely used in
• Proteomics
• Biochemistry
• Forensics
• Genetics
• Molecular biology
Polyacrylamide gels separate
proteins and small pieces of DNA
• Major components of polyacrylamide gels
• Acrylamide – matrix material/ NEUROTOXIN
• Bis-acrylamide - cross-linking agent/ NEUROTOXINS
• TEMED - catalyst
• Ammonium persulfate - free radical initiator
H
N
H
N
O O
Bisacrylamide
(cross-linking agent)
NH2
O
Acrylamide
(matrix material)
SO4
TEMED
(catalyst)
Ammonium persulfate
(free radical initiator)
Polyacrylamide
(non-toxic)
Polymerization
N N
Polyacrylamide
(non-toxic)
Polyacrylamide
O
NH
C H2
NH
O
O
NH
CH2
NH
O
C ON H
2 CON H
2
C ON H
2
CONH
Bis-acrylamide
cross links
Sodium dodecyl sulfate - SDS
The anionic detergent SDS unfolds or
denatures proteins
• Uniform linear shape
• Uniform charge/mass
ratio
Cathode (-)
Anode (+)
Standard Sample1 Sample2
One-dimensional polyacrylamide
gel electrophoresis (SDS-PAGE)
During SDS-PAGE proteins separate
according to their molecular weight
Bromophenol
Blue dye front
Cathode (-)
Anode (+)
Standard Sample1 Sample2
20 kDa
100 kDa
75 kDa
50 kDa
37 kDa
25 kDa
150 kDa
Image of Real SDS-PAG
20 kDa
250 kiloDaltons
150 kDa
100 kDa
75 kDa
50 kDa
37 kDa
25 kDa
Cathode
Anode
Separation of Protein X
Bromophenol
Blue dye front
Cathode (-)
Anode (+)
Standard Sample1 Sample2
20 kDa
100 kDa
75 kDa
50 kDa
37 kDa
25 kDa
150 kDa
Protein X
11 kDa
25 kDa
Two-dimensional gel
electrophoresis (2-DGE)
Most widely used protein separation technique in
proteomics
Capable of resolving thousands of proteins from a
complex sample (i.e. blood, organs, tissue…)
1st dimension - isoelectric focusing
2nd dimension - SDS-PAGE
Isoelectric focusing (IEF) is separation of
proteins according to native charge.
isoelectric point -pH at which net charge is zero
1st Dimension-Isoelectric
Focusing
2-DGE
protein
samples
IEF
1st dimension
SDS-PAGE
2nd dimension
Neutral at pH 3
20 kDa
100 kDa
75 kDa
50 kDa
37 kDa
25 kDa
150 kDa
11 kDa
pH gradient 10
3
pI
mass
100
75
50
25
3 10
Arabidopsis developing leaf
kDa
2-DG
4 5 6 7 8 9
2-DGE
SDS-PAGE
2nd dimension
20 kDa
100 kDa
75 kDa
50 kDa
37 kDa
25 kDa
150 kDa
11 kDa
10
3 4 5 6 7 8 9
Protein X
25 kDa
pI 5
1-DGE vs. 2-DGE
1-DGE (SDS-PAGE)
• High reproduciblity
• Quick/Easy
• Separates solely based
on size
• Modest resolution,
dependent on complexity
of sample
2-DGE
• Modest reproducibility
• Slow/Demanding
• Separates based on pI and
size
• High resolution, not
dependent on complexity
of sample
Summary – protein separation
•Protein separation takes advantage physical
properties such as isoelectric point and molecular
weight
•SDS-PAGE is a widely used technique to separate
proteins
•1-DGE is a quick and easy method to separate protein
by size only
•2-DGE combines isoeletric focusing (IEF) and SDS-
PAGE to separate proteins by pI and size
Protein identification
mass spectrometry
Peptide mass
fingerprinting
intact protein x
protein digestion
mass spectrometry
m/z
intensity
952.0984
1895.9057
1345.6342
899.8743
2794.9761
mass
Protein ID
Make proteolytic peptide
fragments - Digest the
protein into peptides (using
trypsin)
Measure peptide masses -
“Weigh” the peptides in a
mass spectrometer
Match peptide masses to
protein or nucleotide
sequence database - Compare
the data to known proteins
and look for a match
Protein digestion
We use the enzyme TRYPSIN to digest (cut) proteins
into peptides – trypsin cuts after Lysine (K) and
Arginine (R)
????????K?????R????????
????????K?????R????????
????????K?????R????????
Protein X
????????K?????R????????
????????K?????R????????
????????K?????R????????
How does mass spectrometry
identify unknown proteins?
Basics of mass spectrometry
• determination of mass to charge ratio
(m/z)
• Mass spectrometer = very accurate
weighing scales
– third or fourth decimal place
????????K
?????R
????????
We then “weigh” these peptides
with a Mass Spectrometer
Mass Spectrometer
????????K
?????R
????????
We then “weigh” these peptides
with a Mass Spectrometer
692.31 Da
1106.55 Da
1002.37Da
Mass of peptides should be compared to
theoretical masses of known peptides
?????R = 692.31 Da
????????K = 1106.55 Da
???????? = 1002.37Da
Computation of theoretical masses of
known peptides known
Computer Peptides
• WEGETMILK 1106.55
• ADEMTYEK 1105.23
• PLMEHGAK 1089.50
• LMEHHH 782.25
• ASTEER 692.31
• DMGEYIILES 1056.92
• EGEDMPAFY 1002.35
• CYHGMEI 984.36
• EFPKLYSEK 900.56
• YSEPYSSIIR 1102.34
• IESPLMIA 864.35
• AEFLYSR 600.21
• DLMILIYR 864.97
• METHIPEEK 795.36
• KISSMER 513.21
• PEPTIDEK 456.23
• MANYCQWS 792.15
• TYSMEDGHK 678.46
• YMEPSATFGHR 995.46
• GHLMEDFSAC 896.35
• HHFAASTR 564.88
• ALPMESS 469.12
Proteome = all protein sequences
Digest Proteome with
simulated Trypsin
Mass of peptides compared to
theoretical masses of all peptides
known, using a computer program.
?????R = 692.31 Da
????????K = 1106.55 Da
???????? = 1002.37Da
Computer Peptides
• WEGETMILK 1106.55
• ADEMTYEK 1105.23
• PLMEHGAK 1089.50
• LMEHHH 782.25
• ASTEER 692.31
• DMGEYIILES 1056.92
• EGEDMPAFY 1002.35
• CYHGMEI 984.36
• EFPKLYSEK 900.56
• YSEPYSSIIR 1102.34
• IESPLMIA 864.35
• AEFLYSR 600.21
• DLMILIYR 864.97
• METHIPEEK 795.36
• KISSMER 513.21
• PEPTIDEK 456.23
• MANYCQWS 792.15
• TYSMEDGHK 678.46
• YMEPSATFGHR 995.46
• GHLMEDFSAC 896.35
• HHFAASTR 564.88
• ALPMESS 469.12
Mass of peptides matched to
theoretical masses known peptides,
using a computer program.
?????R = 692.31 Da
????????K = 1106.55 Da
???????? = 1002.37Da
Computer Peptides
• WEGETMILK 1106.55
• ADEMTYEK 1105.23
• PLMEHGAK 1089.50
• LMEHHH 782.25
• ASTEER 692.31
• DMGEYIILES 1056.92
• EGEDMPAFY 1002.35
• CYHGMEI 984.36
• EFPKLYSEK 900.56
• YSEPYSSIIR 1102.34
• IESPLMIA 864.35
• AEFLYSR 600.21
• DLMILIYR 864.97
• METHIPEEK 795.36
• KISSMER 513.21
• PEPTIDEK 456.23
• MANYCQWS 1002.37
• TYSMEDGHK 678.46
• YMEPSATFGHR 995.46
• GHLMEDFSAC 896.35
• HHFAASTR 564.88
• ALPMESS 469.12
The unknown peptides have been
identified
?????R = 692.31 Da
????????K = 1106.55 Da
???????? = 1002.37Da
WEGETMILK
ASTEER
MANYCQWS
Protein X has been identified
????????K?????R????????
????????K?????R????????
????????K?????R????????
WEGETMILK AFTEER MANYCQWS
Summary – tools to study proteins?
•Proteins are digested into peptides
•Peptides are analyzed with a mass spectrometer
•Match observed peptide masses to theoretical
masses of all peptides in database
•Assemble those peptide matches into a protein
identification
Concluding points about Proteomics
-Proteomics is the analysis of all proteins
-Interdisciplinary research
-Essential to both basic and clinical research
-Protein are the workhorses of the cell
- Discovery research – drugs and diseases
-Proteomics tools allow identification of proteins
Questions

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Proteinomics

  • 1. Department of Pharmacology MPL 104 T – CMP Unit - IV 03-05-2021
  • 3. Proteomics is the analysis of the protein complement to the genome Genomics Proteomics Gene Transcript Protein
  • 5. Proteomics Research •Basic research: To understand the molecular mechanisms underlying life. •Applied research: Clinical testing for proteins associated with pathological states (e.g. cancer).
  • 6. Applications of Proteomics Proteomics Structural Proteomics Proteome Mining Post- translational Modifications Protein Expression Profiling Functional Proteomics Protein- protein Interactions Glycoyslation Phosphorylation Proteolysis Yeast two-hybrid Co-precipitation Phage Display Drug Discovery Target ID Differential Display Yeast Genomics Affinity Purified Protein Complexes Mouse Knockouts Medical Microbiology Signal Transduction Disease Mechanisms Organelle Composition Subproteome Isolation Protein Complexes
  • 7. For example: Hemoglobin Picks up oxygen in the lungs, travels through the blood, and delivers it to the cells. O2 hemoglobin Hbβ Hbα Hbβ Hbα
  • 8. ATG GTG CAC CTG ACT CCT GAG GAG … ATG GTG CAC CTG ACT CCT GTG GAG … E E M V H L T P … E V M V H L T P … Normal Hbβ Mutated Hbβ Sickle cell disease is caused by a single amino acid change.
  • 9. Summary – what is proteomics? •Involves the study of proteins •Proteomics is multidisciplinary •Proteomics is being applied to both basic and clinical research
  • 11. What are PROTEINS? Proteins are large, complex molecules that serve diverse functional and structural roles within cells.
  • 12. Transport Hemoglobin Carries O2 Defense Antibody Fights Viruses Enzyme Protease Degrades Protein Support Keratin Forms Hair and Nails Motion Actin Contracts Muscles Regulation Insulin Controls Blood Glucose Proteins do most of the work in the cell
  • 13. Proteins are comprised of amino acid building blocks R O OH C N H H Acid Base Variable CH + H2O Dipeptide Peptide Bond Amino acid 1 Amino acid 2 R1 O C C N O H H2 H R2 H C C N O O H H H R1 O C C R2 O C C H H N H2 N H OH
  • 14. Summary – why study proteins? •Biological workhorses that carry out most of the functions within the cell •Serve diverse functional and structural roles •Composed of amino acids that are covalently linked by peptide bonds •Synthesized during the translation process •Must fold correctly to perform their functions
  • 16. Proteomic tools to study proteins • Protein isolation • Protein separation • Protein identification
  • 18. How are proteins isolated? • Mechanical Methods – grinding – break open cell – centrifugation – remove insoluble debris • Chemical Methods – detergent – breaks open cell compartments – reducing agent – breaks specific protein bonds – heat – break peptide bonds to “linearize” protein
  • 19. Protein isolation procedure Find a sample Pick it Grind sample in buffer Transfer to tube Heat the sample Centrifuge to remove insoluble material “pure” protein solution Recover supernatant Keep solution for gel analysis
  • 21. Summary – protein isolation •Proteins can be isolated from a variety of samples •Proteomics includes the use of both mechanical and chemical methods to isolate proteins •Opening cell or cellular compartments •Breaking bonds and “linearizing” proteins •Removal cell debris
  • 23. Why separate proteins? “PURE” Protein Solution Tube 1 Decreased Protein ID Increased Complexity Tube 2 Increased Protein ID Decreased Complexity
  • 24. How to separate proteins? Separating intact proteins is to take advantage of their diversity in physical properties, especially isoelectric point and molecular weight
  • 25. Methods of Protein Separation • Sodium Dodecyl Sulfate – Polyacrylamide Gel Electrophoresis (SDS-PAGE) • Isoelectric Focusing (IEF)
  • 26. SDS-PolyAcrylamide Gel Electrophoresis (SDS-PAGE) is a widely used technique to separate proteins in solution
  • 27. SDS-PAGE separates only by molecular weight • Molecular weight is mass one molecule • Dalton (Da) is a small unit of mass used to express atomic and molecular masses.
  • 28. PAGE is widely used in • Proteomics • Biochemistry • Forensics • Genetics • Molecular biology
  • 29. Polyacrylamide gels separate proteins and small pieces of DNA • Major components of polyacrylamide gels • Acrylamide – matrix material/ NEUROTOXIN • Bis-acrylamide - cross-linking agent/ NEUROTOXINS • TEMED - catalyst • Ammonium persulfate - free radical initiator
  • 30. H N H N O O Bisacrylamide (cross-linking agent) NH2 O Acrylamide (matrix material) SO4 TEMED (catalyst) Ammonium persulfate (free radical initiator) Polyacrylamide (non-toxic) Polymerization N N
  • 31. Polyacrylamide (non-toxic) Polyacrylamide O NH C H2 NH O O NH CH2 NH O C ON H 2 CON H 2 C ON H 2 CONH Bis-acrylamide cross links
  • 32. Sodium dodecyl sulfate - SDS The anionic detergent SDS unfolds or denatures proteins • Uniform linear shape • Uniform charge/mass ratio
  • 33. Cathode (-) Anode (+) Standard Sample1 Sample2 One-dimensional polyacrylamide gel electrophoresis (SDS-PAGE)
  • 34. During SDS-PAGE proteins separate according to their molecular weight Bromophenol Blue dye front Cathode (-) Anode (+) Standard Sample1 Sample2 20 kDa 100 kDa 75 kDa 50 kDa 37 kDa 25 kDa 150 kDa
  • 35. Image of Real SDS-PAG 20 kDa 250 kiloDaltons 150 kDa 100 kDa 75 kDa 50 kDa 37 kDa 25 kDa Cathode Anode
  • 36. Separation of Protein X Bromophenol Blue dye front Cathode (-) Anode (+) Standard Sample1 Sample2 20 kDa 100 kDa 75 kDa 50 kDa 37 kDa 25 kDa 150 kDa Protein X 11 kDa 25 kDa
  • 37. Two-dimensional gel electrophoresis (2-DGE) Most widely used protein separation technique in proteomics Capable of resolving thousands of proteins from a complex sample (i.e. blood, organs, tissue…) 1st dimension - isoelectric focusing 2nd dimension - SDS-PAGE
  • 38. Isoelectric focusing (IEF) is separation of proteins according to native charge. isoelectric point -pH at which net charge is zero 1st Dimension-Isoelectric Focusing
  • 39. 2-DGE protein samples IEF 1st dimension SDS-PAGE 2nd dimension Neutral at pH 3 20 kDa 100 kDa 75 kDa 50 kDa 37 kDa 25 kDa 150 kDa 11 kDa pH gradient 10 3
  • 41. 2-DGE SDS-PAGE 2nd dimension 20 kDa 100 kDa 75 kDa 50 kDa 37 kDa 25 kDa 150 kDa 11 kDa 10 3 4 5 6 7 8 9 Protein X 25 kDa pI 5
  • 42. 1-DGE vs. 2-DGE 1-DGE (SDS-PAGE) • High reproduciblity • Quick/Easy • Separates solely based on size • Modest resolution, dependent on complexity of sample 2-DGE • Modest reproducibility • Slow/Demanding • Separates based on pI and size • High resolution, not dependent on complexity of sample
  • 43. Summary – protein separation •Protein separation takes advantage physical properties such as isoelectric point and molecular weight •SDS-PAGE is a widely used technique to separate proteins •1-DGE is a quick and easy method to separate protein by size only •2-DGE combines isoeletric focusing (IEF) and SDS- PAGE to separate proteins by pI and size
  • 45. Peptide mass fingerprinting intact protein x protein digestion mass spectrometry m/z intensity 952.0984 1895.9057 1345.6342 899.8743 2794.9761 mass Protein ID Make proteolytic peptide fragments - Digest the protein into peptides (using trypsin) Measure peptide masses - “Weigh” the peptides in a mass spectrometer Match peptide masses to protein or nucleotide sequence database - Compare the data to known proteins and look for a match
  • 46. Protein digestion We use the enzyme TRYPSIN to digest (cut) proteins into peptides – trypsin cuts after Lysine (K) and Arginine (R) ????????K?????R???????? ????????K?????R???????? ????????K?????R???????? Protein X ????????K?????R???????? ????????K?????R???????? ????????K?????R????????
  • 47. How does mass spectrometry identify unknown proteins?
  • 48. Basics of mass spectrometry • determination of mass to charge ratio (m/z) • Mass spectrometer = very accurate weighing scales – third or fourth decimal place
  • 49. ????????K ?????R ???????? We then “weigh” these peptides with a Mass Spectrometer Mass Spectrometer
  • 50. ????????K ?????R ???????? We then “weigh” these peptides with a Mass Spectrometer 692.31 Da 1106.55 Da 1002.37Da
  • 51. Mass of peptides should be compared to theoretical masses of known peptides ?????R = 692.31 Da ????????K = 1106.55 Da ???????? = 1002.37Da
  • 52. Computation of theoretical masses of known peptides known Computer Peptides • WEGETMILK 1106.55 • ADEMTYEK 1105.23 • PLMEHGAK 1089.50 • LMEHHH 782.25 • ASTEER 692.31 • DMGEYIILES 1056.92 • EGEDMPAFY 1002.35 • CYHGMEI 984.36 • EFPKLYSEK 900.56 • YSEPYSSIIR 1102.34 • IESPLMIA 864.35 • AEFLYSR 600.21 • DLMILIYR 864.97 • METHIPEEK 795.36 • KISSMER 513.21 • PEPTIDEK 456.23 • MANYCQWS 792.15 • TYSMEDGHK 678.46 • YMEPSATFGHR 995.46 • GHLMEDFSAC 896.35 • HHFAASTR 564.88 • ALPMESS 469.12 Proteome = all protein sequences Digest Proteome with simulated Trypsin
  • 53. Mass of peptides compared to theoretical masses of all peptides known, using a computer program. ?????R = 692.31 Da ????????K = 1106.55 Da ???????? = 1002.37Da Computer Peptides • WEGETMILK 1106.55 • ADEMTYEK 1105.23 • PLMEHGAK 1089.50 • LMEHHH 782.25 • ASTEER 692.31 • DMGEYIILES 1056.92 • EGEDMPAFY 1002.35 • CYHGMEI 984.36 • EFPKLYSEK 900.56 • YSEPYSSIIR 1102.34 • IESPLMIA 864.35 • AEFLYSR 600.21 • DLMILIYR 864.97 • METHIPEEK 795.36 • KISSMER 513.21 • PEPTIDEK 456.23 • MANYCQWS 792.15 • TYSMEDGHK 678.46 • YMEPSATFGHR 995.46 • GHLMEDFSAC 896.35 • HHFAASTR 564.88 • ALPMESS 469.12
  • 54. Mass of peptides matched to theoretical masses known peptides, using a computer program. ?????R = 692.31 Da ????????K = 1106.55 Da ???????? = 1002.37Da Computer Peptides • WEGETMILK 1106.55 • ADEMTYEK 1105.23 • PLMEHGAK 1089.50 • LMEHHH 782.25 • ASTEER 692.31 • DMGEYIILES 1056.92 • EGEDMPAFY 1002.35 • CYHGMEI 984.36 • EFPKLYSEK 900.56 • YSEPYSSIIR 1102.34 • IESPLMIA 864.35 • AEFLYSR 600.21 • DLMILIYR 864.97 • METHIPEEK 795.36 • KISSMER 513.21 • PEPTIDEK 456.23 • MANYCQWS 1002.37 • TYSMEDGHK 678.46 • YMEPSATFGHR 995.46 • GHLMEDFSAC 896.35 • HHFAASTR 564.88 • ALPMESS 469.12
  • 55. The unknown peptides have been identified ?????R = 692.31 Da ????????K = 1106.55 Da ???????? = 1002.37Da WEGETMILK ASTEER MANYCQWS
  • 56. Protein X has been identified ????????K?????R???????? ????????K?????R???????? ????????K?????R???????? WEGETMILK AFTEER MANYCQWS
  • 57. Summary – tools to study proteins? •Proteins are digested into peptides •Peptides are analyzed with a mass spectrometer •Match observed peptide masses to theoretical masses of all peptides in database •Assemble those peptide matches into a protein identification
  • 58. Concluding points about Proteomics -Proteomics is the analysis of all proteins -Interdisciplinary research -Essential to both basic and clinical research -Protein are the workhorses of the cell - Discovery research – drugs and diseases -Proteomics tools allow identification of proteins