Characterising complex binding interactions by ...

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Characterising complex binding interactions by microcalorimetry

Isothermal Titration Calorimetry &

Differential Scanning Calorimetry

Articles written with isothermal titration calorimetry

content since 1990 sourced from the Web of Science ™.

Falconer, R.J. (2016) Applications of isothermal titration calorimetry - the research and technical developments

from 2011-15. Journal of Molecular Recognition, 29: 504–515.

Differential Scanning Calorimetry

20 40 60 80 100-0.005

0.000

0.005

0.010

0.015

First scan

Subsequent scans

Temperature (Celsius)

Heat

cap

acit

y (

kJ/K

)

Thermal scan of grape invertase

0 20 40 60 80-0.0010

-0.0005

0.0000

0.0005

0.0010First scan

Subsequent scans

Temperature (Celsius)

Heat

cap

acit

y (

kJ/K

)

Thermal scan of grape thaumatin-like protein using a DSC

Differential Scanning Calorimetry

Sanchez-Ruiz, et al. Biochemistry, 1988, 27, 1648-1652.

k = v Cp / (Qt - Q)

0.00300 0.00305 0.00310 0.00315 0.00320-6

-5

-4

-3

-2

-1

0

1

2

1/T

lnk

Arrhenius Equation

k = A exp(-E/RT)

Estimate the activation energy of unfolding

0 10 20 30 40-0.024

-0.023

-0.022

-0.021

-0.020

Temperature (ºC)

He

at

cap

acit

y (k

J/°

C)

0 10 20 30 40-0.024

-0.023

-0.022

-0.021

-0.020

Temperature (ºC)

He

at

cap

acit

y (k

J/°° °°

C)

Differential scanning calorimetry of cryoglobulins (a) the downward thermal scan showing cold-induced

aggregation, (b) upward thermal scan showing heat-induced disassociation, the cryoglobulin Pot IgM

(black) and Yvo IgM (green).

Thermal scan of IGM cold-induced precipitation using a DSC

Differential Scanning Calorimetry

Meliga, S.C.; Farrugia, W.; Ramsland, P.A.; Falconer, R.J. (2013) Cold-induced precipitation of a monoclonal IgM; a negative

activation enthalpy reaction. Journal of Physical Chemistry B, 117: 490-494.

Thermal scan of grape lipid-transfer protein using a DSC

Differential scanning calorimetry of grape lipid-transfer protein purified from Vitis vinifera

Differential Scanning Calorimetry

Differential Scanning Calorimetry

Pressure perturbation calorimetry of sodium dihydrogen phosphate and isopropanol solutions.

Pressure perturbation calorimetry using a DSC

Bye, J.W.; Freeman, C.L.; Howard, J.D.; Herz, G.; McGregor, J.; Falconer, R.J. (2017) Pressure perturbation calorimetry analysis of

the mesoscopic structuring of 2-propanol/water mixtures. Journal of Solution Chemistry, 46: 175-189.

Isothermal Titration Calorimetry

Stoichiometry

Association constant Ka

Thermodynamic constants

ΔH, TΔS & ΔG

ΔG = -RTlnKa

ΔG = ΔH - TΔS

McRae, J.M.; Falconer, R.J.; Kennedy, J.A. (2010) Thermodynamics of

grape and wine tannin interaction with polyproline: implications for

red wine astringency. Journal of Agricultural and Food Chemistry, 58:

12510–12518.

HO O

OH

OH

R1

OH

R2

R3

O

O

OH

OH

OH

1 R1=OH, R2,R3=H2 R1,R3=H, R2=OH3 R1=Galloyl, R2=OH, R3=H4 R1=H, R2,R3=OH

Galloyl=

HO+O

OH

OH

OH

OH

OGlucose

5

2

4

8

6

B

A

N

NO

O

n

O

OH

O

OH

O

OH

HO

HO

OH

OH

OH

OH

OH

OH

OH

OH

OH

HO

O

OH

O

OH

O

HO

HO

O

OH

OH

HO

HO

OH

OH

OH

OH

O

OOH

OH

O

OH

HO

O

OH

HO

OH

OH

HO

O

OH

OH

OH

OHHO

O

OH

OH

OH

OHHO

a. b.

Polyphenolics – Polyproline Binding

Wine polyphenolics – Polyproline Binding

McRae, J.M.; Falconer, R.J.; Kennedy, J.A. (2010) Thermodynamics of grape and wine tannin interaction with

polyproline: implications for red wine astringency. Journal of Agricultural and Food Chemistry, 58: 12510–12518.

Dual interactions

Hydrophobic interaction and H-bonding

10 ºC 45 ºC

Polyphenolics – BSA Binding

Isothermal titration calorimetry of the interaction of the proanthocyanidin trimer, pentamer, hexamer

with BSA showing the thermogram and binding isotherm. All at pH 4.0 in a 10 mM ammonium acetate

buffer at 10 oC.

Kilmister, R.L.; Faulkner, P.; Downey, M.O.; Darby, S.J.; Falconer, R.J. (2016) The complexity of condensed tannin binding to

bovine serum albumin - An isothermal titration calorimetry study. Food Chemistry, 190: 173-178.

Polyphenolics – BSA Binding

Isothermal titration calorimetry of the interaction of the proanthocyanidin tetramer with BSA at different

temperatures a) 10 oC and b) 25 oC and c) 10 oC with 100 mM NaCl showing the thermogram and binding

isotherm. All at pH 4.0 in a 10 mM ammonium acetate buffer.

Kilmister, R.L.; Faulkner, P.; Downey, M.O.; Darby, S.J.; Falconer, R.J. (2016) The complexity of condensed tannin binding to

bovine serum albumin - An isothermal titration calorimetry study. Food Chemistry, 190: 173-178.

Electrostatic interaction – Phytate with lysozyme

Electrostatic interaction – Phytate with lysozyme

Isothermal titration calorimetry (ITC) titration of phytate (6mM) into lysozyme (0.4mM) in 10mM

ammonium acetate buffer pH 4 at 25 °C showing the thermogram (top) and binding isotherm (bottom).

Electrostatic interaction – Phytate with lysozyme

Isothermal titration calorimetry (ITC) titration of phytate (6mM) into lysozyme (0.4mM) in 10mM

ammonium acetate buffer pH 4 at 40 °C showing the thermogram (top) and binding isotherm (bottom).

Electrostatic interaction – Phytate with lysozyme

Darby, S.J.; Platts, L.; Daniel, M.S.; Cowieson, A.J.; Falconer, R.J. (2017) An isothermal titration calorimetry study of phytate

binding to lysozyme: A multisite electrostatic binding reaction. Journal of Thermal Analysis and Calorimetry, 127: 1201–

1208.

Isothermal Titration Calorimetry

Lambert, F.L. (2002) Entropy is simple, qualitatively. Journal of Chemical Education, 79: 1241-1246.

Leff, H.S. (1996) Thermodynamic entropy: The spreading and sharing of energy. American Journal of

Physics, 64: 1261-1271.

Falconer, R.J. (2016) Applications of isothermal titration calorimetry - the research and technical

developments from 2011-15. Journal of Molecular Recognition, 29: 504–515.

What have we learnt?

Binding interactions involve water displacement

Water displacement is usually endothermic while bond formation is exothermic

ΔHobserved = ΔHbonding + ΔHwater

ΔG = ΔH - TΔS

How do you interpret the entropy values?

For an modern explanation of entropy read Franks Lambert and Harvey Leff’s papers

Thank you