TY - JOUR
T1 - Kinetics of tetramolecular quadruplexes
AU - Mergny, Jean Louis
AU - De Cian, Anne
AU - Ghelab, Amar
AU - Saccà, Barbara
AU - Lacroix, Laurent
N1 - Funding Information:
This manuscript is dedicated to the memory of Professor Claude Hélène (1938–2003). We thank M. Rougée (MNHN, Paris, France) and C. Gosse (CNRS/LPN Marcoussis, France) for helpful discussions and both referees for helpful suggestions. This work was supported by an ARC grant (#3365 to J.L.M.). Funding to pay the Open Access publication charges for this article was provided by the INSERM.
PY - 2005/3/7
Y1 - 2005/3/7
N2 - The melting of tetramolecular DNA or RNA quadruplexes is kinetically irreversible. However, rather than being a hindrance, this kinetic inertia allows us to study association and dissociation processes independently. From a kinetic point of view, the association reaction is fourth order in monomer and the dissociation first order in quadruplex. The association rate constant kon, expressed in M-3·S-1 decreases with increasing temperature, reflecting a negative activation energy (Eon) for the sequences presented here. Association is favored by an increase in monocation concentration. The first-order dissociation process is temperature dependent, with a very positive activation energy Eoff, but nearly ionic strength independent. General rules may be drawn up for various DNA and RNA sequence motifs, involving 3-6 consecutive guanines and 0-5 protruding bases. RNA quadruplexes are more stable than their DNA counterparts as a result of both faster association and slower dissociation. In most cases, no dissociation is found for G-tracts of 5 guanines or more in sodium, 4 guanines or more in potassium. The data collected here allow us to predict the amount of time required for 50% (or 90%) quadruplex formation as a function of strand sequence and concentration, temperature and ionic strength.
AB - The melting of tetramolecular DNA or RNA quadruplexes is kinetically irreversible. However, rather than being a hindrance, this kinetic inertia allows us to study association and dissociation processes independently. From a kinetic point of view, the association reaction is fourth order in monomer and the dissociation first order in quadruplex. The association rate constant kon, expressed in M-3·S-1 decreases with increasing temperature, reflecting a negative activation energy (Eon) for the sequences presented here. Association is favored by an increase in monocation concentration. The first-order dissociation process is temperature dependent, with a very positive activation energy Eoff, but nearly ionic strength independent. General rules may be drawn up for various DNA and RNA sequence motifs, involving 3-6 consecutive guanines and 0-5 protruding bases. RNA quadruplexes are more stable than their DNA counterparts as a result of both faster association and slower dissociation. In most cases, no dissociation is found for G-tracts of 5 guanines or more in sodium, 4 guanines or more in potassium. The data collected here allow us to predict the amount of time required for 50% (or 90%) quadruplex formation as a function of strand sequence and concentration, temperature and ionic strength.
U2 - 10.1093/nar/gki148
DO - 10.1093/nar/gki148
M3 - Article
C2 - 15642696
AN - SCOPUS:13744249293
SN - 0305-1048
VL - 33
SP - 81
EP - 94
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 1
ER -