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Antibody based assay –Pitfall and practical issue. 2012 05 30 Seok-Hyung Kim. Antibody based assay. 1. The chemical basis for Ab -reaction 2. How to choose good antibody 3. How to reduce non-specific reaction. Structure of Antibody. Heavy chain :Variable region + constant region
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Antibody based assay –Pitfall and practical issue 2012 05 30Seok-Hyung Kim
Antibody based assay 1. The chemical basis for Ab-reaction 2. How to choose good antibody 3. How to reduce non-specific reaction
Structure of Antibody • Heavy chain :Variable region + constant region (isotype ) => class of antibody • Light chain : Variable region + constant region (kappa / lambda chain)
Beta pleated sheet containing two anti-Parallel beta strands
Ab-Ag interaction Computer simulation of an antibody-antigen Interaction between antibody and influenza Virus antigen(a globular protein)
Ag contact area : flat undulating face • 650 – 900 A (15 – 22 amino acid) • small antigen : antigen binding site is generally smaller and appear more like a deep pocket in which ligand is largely buried
Solvent accessible surface of an anti-hemagglutinin Fab fragment Bound Fab fragment Unbound Fab fragment
Maturation of an antibody response is governed by modulations in flexibility of antigen combining site (immunity 2000 13: 611-620) Pliable germline antigen combining site epitope templated structural rigidity maturation
Result (1) • Temperature dependence of antigen affinities of antibodies from primary and secondary responses • 25 -> 35’C : IgM : affinity 3 – 100 folds decrease IgG : No difference ; Qualitative difference
Model synthetic peptide antigen : PS1CT3 Table 1 Temperature dependance
Temperature differentially affects antigen association rates of primary and secondary mAbs
Result(2) The cause of contradictory Effectsof Temperature on Antigen Association Rates between Primary and Secondary Responses : Change of Entropy G= H-TS • Enthalpy(H) : Heat change • Entrophy(S) : net conformational, stereochemical structural perturbations
Chemical bond used in Ag-Ab interaction (1) • Covalent bond : not used • Hydrogen bond : important for Ag-Ab • Ionic bond : infrequently used • Van derwaals bond : frequently used but not important • Hydrophobic interaction : important for Ag-Ab
Result (2) • Primary Ab(IgM) : enthalpy diriven entropy constrained • Secondary Ab : entropy driven Enthalpy란 면에선 불리
Result(3) • Germ line antibody 7cM(PS1CT3), 36-65(Ars), BBE6.12H3(NP) 37’C : high degree of cross reactivity 4’C : no cross reactivity • Mature antibody Cys18(PS1CT3), P16.7(Ars), Bg110-2(NP) 37’C, 4’C : no cross reactivity
Discussion(1) • Germ line antibody affinity at high temperature cross reactivity at high temperature => multiple conformational state > induced fit trasition from one conformation to another
Discussion (2) • Entropic constraint of germline Ab. : Free germline paratope exist in an equilibrium between multiple conformational states, only subset of which are capable of binding to the Ag
Molecular dynamics and free energy calculations applied to affinity maturation In antibody 48G7 Increasing the rigidity of the antibody structure further optimizes the binding affinity of the antibody for the hapten (PNAS 1999 96: 14330)
rms fluctuations of the germ line and mature antibody hapten complexes. rms fluctuations are defined as rms deviations of the structure at a given time from the average structure of the MD simulation (PNAS 1999 96: 14330)
Structural Insights into the Evolution of an Antibody Combining Site Many germline antibodies may indeed adopt multipleconfigurations with antigen binding, together with somatic mutation,stabilizing the configuration with optimum complementarity toantigen (Science 1997 : 276; 1665)
Conclusion Flexibility Rigidity Germline Ab Versatile Low affinity Screening &recognition Temperature sensitive Polyspecific Multiple configuration Secondary Ab Specific High affinity Response Cross-reactive
Applications of Antibody Types of antigen (epitope) 3D conformation Linear form 1. Immunohistochemisty 2. Flow cytometric analysis 3. Immunoprecipitation (IP, ChIP) 4. ELISA 1. Immunoblotting (Western blotting)
Antibody based assay 1. The chemical basis for Ab-reaction 2. How to choose good antibody 3. How to reduce non-specific reaction
How to choose good antibody • A good antibody? : High affinity : Entropy driven antibody • A good antibody : low risk-low return : generally expensive (DAKO, Novo…) : restriction in variety
How to choose good antibody • A bad antibody : High risk-high return : generally less expensive (santacruz) : much less restriction in variety : but require highly skillful expert.
Good antibody / bad antibody 역가가 낮은 항체 Control Control 측정값 측정값 항체를 저농도로 사용시 항체를 고농도로 사용시 역가가 높은 항체 Control Control 측정값 측정값 항체를 저농도로 사용시 항체를 고농도로 사용시
Structural difference in good / bad antibody (1) • Bad antibody : structurally more flexible 37’C : high degree of cross reactivity : multiple conformational state 4’C: no cross reactivity • Good antibody : more rigid 37’C, 4’C : no cross reactivity
Structural difference in good / bad antibody (2) Flexibility Rigidity Germline Ab Versatile Low affinity Temperature sensitive Polyspecific Multiple configuration Secondary Ab Specific High affinity cross-reactive
Antibody based assay 1. The chemical basis for Ab-reaction 2. How to choose good antibody 3. How to reduce non-specific reaction
Non-specific reactivity of Antibody (Unwanted reactivity) • Polyspecificity (Multi-specificity) • : unrelated specificities, which means • interactions caused by different binding • modes. • Cross-reactivity (Molecular mimicry) • : interactions based on wild-type-derived • key residues.
Causes of non-specific reactivity of Antibody based assay 1. Unwanted reaction of Antibody 2. Non-specific reaction of detection kit 3. Non-opitimized buffer
Solution of non-specific reactivity of Antibody based assay Selection of good Antibody 2. Optimization of antibody dilution 3. Simple but sensitive detection kit 4. Opitimization of buffer (ion concentration / blocking agent)
Positive control Negative control
Causes of background staining in immunohistochemistry 1. Non-specific interaction between SA-HRP and tissue : ionic interaction hydrophobic interaction 2. Endogenous biotin 3. Binding of SA-HRP to endogenous lectin 3. Non-specific interaction of 2ndary antibody
TITERING ANTIBODIES SPECIFIC ANTIBODY AMOUNT BOUND NON-SPECIFIC ANTIBODY CONCENTRATION
3 µg s/n = 2.5 1 µg s/n = 2.1 0.3 µg s/n = 2.4 0.1 µg s/n = 4.1 0.03 µg s/n = 4.8 0.01 µg s/n = 4.6 3 0.003 µg s/n = 3.5 0.001 µg s/n = 3.2 auto
5 4 3 2 0 1 2 3 4 5 6 7 8 TITER Signal to Noise Dilution
1 2 3 4 1 2 3 4 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 1 1 2 2 3 3 4 4 isotype control antibody number cytokeratin 1 µg S/N Ab 278 IC 5.8 .3 µg S/N Ab 100 IC 3.6 .01 µg S/N Ab 25.7 IC 2.6
1PBS NaCl : 150mM 1/10 PBS NaCl : 15mM Lymph node : L26(anti-CD20; B cell marker) 면역조직화학의 주요문제 :비특이적 배경염색의 원인
The enhanced reactivity of endogenous biotin-like molecules by the antigen retrieval procedures and signal amplification with tyramine Seok Hyung Kim1, Kyeong Cheon Jung2 , Young Kee Shin1,4, Kyung Mee Lee4, Young S. Park1, Yoon La Choi1, Kwon Ik Oh1, Min Kyung Kim1, Doo Hyun Chung1, Hyung Geun Song3,4 & Seong Hoe Park1,* Histochemical journal 2002 34;97-103