An Overview of the Optical and Electrochemical Methods for Detection of DNA - Drug Interactions
Abstract
A large number of inorganic and organic compounds is able to bind to DNA and form complexes. Among them, drugs are very important, especially chemotherapeutics. This paper presents the overview of DNA structural characteristics and types of interactions (covalent and non-covalent) between DNA molecule and drugs. Covalent binding of the drug is irreversible and leads to complete inhibition of DNA function, what conclusively, causes the cell death. On the other hand, non-covalent binding is reversible and based on the principle of molecular recognition. Special attention is given to elucidation of the specific sites in DNA molecule for drug binding. According to their structural characteristics, drugs that react non-covalently with DNA are mainly intercalators, but also minor and major groove binders. When the complex between drug and DNA is formed, both the drug molecule, as well as DNA, experienced some modifications. This paper presents the overview of the methods used for the study o...f the interactions between DNA and drugs with the aim of detection and explanation of the resulting changes. For this purpose many spectroscopic methods like UV/VIS, fluorescence, infrared and NMR, polarized light spectroscopies like circular and linear dichroism, and fluorescence anisotropy or resonance is used. The development of the electrochemical DNA biosensors has opened a wide perspective using particularly sensitive and selective electrochemical methods for the detection of specific DNA interactions. The presented results summarize literature data obtained by the mentioned methods. The results are used to confirm the DNA damage, to determine drug binding sites and sequence preference, as well as conformational changes due to drug-DNA interaction.
Keywords:
DNA / drug / interaction / spectroscopic methods / electrochemical DNA-biosensorsSource:
Acta Chimica Slovenica, 2014, 61, 3, 555-573Publisher:
- Slovensko Kemijsko Drustvo, Ljubljana
Funding / projects:
Collections
Institution/Community
PharmacyTY - JOUR AU - Aleksić, Mara AU - Kapetanović, Vera PY - 2014 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2138 AB - A large number of inorganic and organic compounds is able to bind to DNA and form complexes. Among them, drugs are very important, especially chemotherapeutics. This paper presents the overview of DNA structural characteristics and types of interactions (covalent and non-covalent) between DNA molecule and drugs. Covalent binding of the drug is irreversible and leads to complete inhibition of DNA function, what conclusively, causes the cell death. On the other hand, non-covalent binding is reversible and based on the principle of molecular recognition. Special attention is given to elucidation of the specific sites in DNA molecule for drug binding. According to their structural characteristics, drugs that react non-covalently with DNA are mainly intercalators, but also minor and major groove binders. When the complex between drug and DNA is formed, both the drug molecule, as well as DNA, experienced some modifications. This paper presents the overview of the methods used for the study of the interactions between DNA and drugs with the aim of detection and explanation of the resulting changes. For this purpose many spectroscopic methods like UV/VIS, fluorescence, infrared and NMR, polarized light spectroscopies like circular and linear dichroism, and fluorescence anisotropy or resonance is used. The development of the electrochemical DNA biosensors has opened a wide perspective using particularly sensitive and selective electrochemical methods for the detection of specific DNA interactions. The presented results summarize literature data obtained by the mentioned methods. The results are used to confirm the DNA damage, to determine drug binding sites and sequence preference, as well as conformational changes due to drug-DNA interaction. PB - Slovensko Kemijsko Drustvo, Ljubljana T2 - Acta Chimica Slovenica T1 - An Overview of the Optical and Electrochemical Methods for Detection of DNA - Drug Interactions VL - 61 IS - 3 SP - 555 EP - 573 UR - https://hdl.handle.net/21.15107/rcub_farfar_2138 ER -
@article{ author = "Aleksić, Mara and Kapetanović, Vera", year = "2014", abstract = "A large number of inorganic and organic compounds is able to bind to DNA and form complexes. Among them, drugs are very important, especially chemotherapeutics. This paper presents the overview of DNA structural characteristics and types of interactions (covalent and non-covalent) between DNA molecule and drugs. Covalent binding of the drug is irreversible and leads to complete inhibition of DNA function, what conclusively, causes the cell death. On the other hand, non-covalent binding is reversible and based on the principle of molecular recognition. Special attention is given to elucidation of the specific sites in DNA molecule for drug binding. According to their structural characteristics, drugs that react non-covalently with DNA are mainly intercalators, but also minor and major groove binders. When the complex between drug and DNA is formed, both the drug molecule, as well as DNA, experienced some modifications. This paper presents the overview of the methods used for the study of the interactions between DNA and drugs with the aim of detection and explanation of the resulting changes. For this purpose many spectroscopic methods like UV/VIS, fluorescence, infrared and NMR, polarized light spectroscopies like circular and linear dichroism, and fluorescence anisotropy or resonance is used. The development of the electrochemical DNA biosensors has opened a wide perspective using particularly sensitive and selective electrochemical methods for the detection of specific DNA interactions. The presented results summarize literature data obtained by the mentioned methods. The results are used to confirm the DNA damage, to determine drug binding sites and sequence preference, as well as conformational changes due to drug-DNA interaction.", publisher = "Slovensko Kemijsko Drustvo, Ljubljana", journal = "Acta Chimica Slovenica", title = "An Overview of the Optical and Electrochemical Methods for Detection of DNA - Drug Interactions", volume = "61", number = "3", pages = "555-573", url = "https://hdl.handle.net/21.15107/rcub_farfar_2138" }
Aleksić, M.,& Kapetanović, V.. (2014). An Overview of the Optical and Electrochemical Methods for Detection of DNA - Drug Interactions. in Acta Chimica Slovenica Slovensko Kemijsko Drustvo, Ljubljana., 61(3), 555-573. https://hdl.handle.net/21.15107/rcub_farfar_2138
Aleksić M, Kapetanović V. An Overview of the Optical and Electrochemical Methods for Detection of DNA - Drug Interactions. in Acta Chimica Slovenica. 2014;61(3):555-573. https://hdl.handle.net/21.15107/rcub_farfar_2138 .
Aleksić, Mara, Kapetanović, Vera, "An Overview of the Optical and Electrochemical Methods for Detection of DNA - Drug Interactions" in Acta Chimica Slovenica, 61, no. 3 (2014):555-573, https://hdl.handle.net/21.15107/rcub_farfar_2138 .