Porphyrin Binding and Irradiation Promote G-Quadruplex DNA Dimeric Structure
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Porphyrin Binding and Irradiation Promote G-Quadruplex DNA Dimeric Structure. / Libera, Valeria; Andreeva, Elena A.; Martel, Anne; Thureau, Aurelien; Longo, Marialucia; Petrillo, Caterina; Paciaroni, Alessandro; Schiro, Giorgio; Comez, Lucia.
In: Journal of Physical Chemistry Letters, Vol. 12, No. 33, 26.08.2021, p. 8096-8102.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Porphyrin Binding and Irradiation Promote G-Quadruplex DNA Dimeric Structure
AU - Libera, Valeria
AU - Andreeva, Elena A.
AU - Martel, Anne
AU - Thureau, Aurelien
AU - Longo, Marialucia
AU - Petrillo, Caterina
AU - Paciaroni, Alessandro
AU - Schiro, Giorgio
AU - Comez, Lucia
PY - 2021/8/26
Y1 - 2021/8/26
N2 - Nucleic acid sequences rich in guanines can organize into noncanonical DNA G-quadruplexes (G4s) of variable size. The design of small molecules stabilizing the structure of G4s is a rapidly growing area for the development of novel anticancer therapeutic strategies and bottom-up nanotechnologies. Among a multitude of binders, porphyrins are very attractive due to their light activation that can make them valuable conformational regulators of G4s. Here, a structure-based strategy, integrating complementary probes, is employed to study the interaction between TMPyP4 porphyrin and a 22-base human telomeric sequence (Tel22) before and after irradiation with blue light. Porphyrin binding is discovered to promote Tel22 dimerization, while light irradiation of the Tel22-TMPyP4 complex controls dimer fraction. Such a change in quaternary structure is found to be strictly correlated with modifications at the secondary structure level, thus providing an unprecedented link between the degree of dimerization and the underlying conformational changes in G4s.
AB - Nucleic acid sequences rich in guanines can organize into noncanonical DNA G-quadruplexes (G4s) of variable size. The design of small molecules stabilizing the structure of G4s is a rapidly growing area for the development of novel anticancer therapeutic strategies and bottom-up nanotechnologies. Among a multitude of binders, porphyrins are very attractive due to their light activation that can make them valuable conformational regulators of G4s. Here, a structure-based strategy, integrating complementary probes, is employed to study the interaction between TMPyP4 porphyrin and a 22-base human telomeric sequence (Tel22) before and after irradiation with blue light. Porphyrin binding is discovered to promote Tel22 dimerization, while light irradiation of the Tel22-TMPyP4 complex controls dimer fraction. Such a change in quaternary structure is found to be strictly correlated with modifications at the secondary structure level, thus providing an unprecedented link between the degree of dimerization and the underlying conformational changes in G4s.
KW - TELOMERE G-QUADRUPLEX
KW - CATIONIC PORPHYRINS
KW - SEQUENCE
KW - ABSORPTION
KW - LIGAND
KW - TMPYP4
U2 - 10.1021/acs.jpclett.1c01840
DO - 10.1021/acs.jpclett.1c01840
M3 - Journal article
C2 - 34406777
VL - 12
SP - 8096
EP - 8102
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
SN - 1948-7185
IS - 33
ER -
ID: 279626485