TY - JOUR
T1 - Method of measuring oligonucleotide-metal affinities
T2 - Interactions of the thrombin binding aptamer with K+ and Sr2+
AU - Wilcox, J. Micah
AU - Rempel, Don L.
AU - Gross, Michael L.
PY - 2008/4/1
Y1 - 2008/4/1
N2 - We report a new, mass spectrometry-based method for measuring affinity constants for specific metal ion binding to DNA, particularly for quadruplex DNA. This method, which is applicable to other systems, utilizes the gas-phase signal fractions, as determined by mass spectrometry, from the bound and unbound species as input into a mathematical model that determines various parameters, one of which is the binding affinity constant. The system used to develop and test the model was the thrombin-binding aptamer, an appropriate quadruplex structure that binds both K+ and Sr2+ cations. Using this method, we measured the binding constants of potassium and strontium cations with the quadruplex structure to be 5000 and 240 nM, respectively. We then applied the method to measure the change in enthalpy of the binding of strontium cations to the thrombin binding aptamer. The ΔH for this interaction is -71 kJ/mol (-17 kcal/mol). The binding constant measurements are consistent with earlier measurements on the same system, and the measured change in enthalpy is in excellent agreement with previous work.
AB - We report a new, mass spectrometry-based method for measuring affinity constants for specific metal ion binding to DNA, particularly for quadruplex DNA. This method, which is applicable to other systems, utilizes the gas-phase signal fractions, as determined by mass spectrometry, from the bound and unbound species as input into a mathematical model that determines various parameters, one of which is the binding affinity constant. The system used to develop and test the model was the thrombin-binding aptamer, an appropriate quadruplex structure that binds both K+ and Sr2+ cations. Using this method, we measured the binding constants of potassium and strontium cations with the quadruplex structure to be 5000 and 240 nM, respectively. We then applied the method to measure the change in enthalpy of the binding of strontium cations to the thrombin binding aptamer. The ΔH for this interaction is -71 kJ/mol (-17 kcal/mol). The binding constant measurements are consistent with earlier measurements on the same system, and the measured change in enthalpy is in excellent agreement with previous work.
UR - http://www.scopus.com/inward/record.url?scp=41849092336&partnerID=8YFLogxK
U2 - 10.1021/ac701903w
DO - 10.1021/ac701903w
M3 - Article
C2 - 18318508
AN - SCOPUS:41849092336
SN - 0003-2700
VL - 80
SP - 2365
EP - 2371
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 7
ER -