engleski

Small molecule markers for DNA, RNA and proteins: balance between selectivity and multitarget applicability

Ligands targeting DNA, RNA and/or proteins have many biochemical and biomedical applications, whereby one of the most widespread uses is spectrophotometric markers. For instance, fluorescent markers and techniques significantly developed within the last decades and now represent about 70% of the detection enabling technologies used in molecular biology and medicine. However, the design of low molecular weight ligand (Mw<600) for recognition of ds-DNA/RNA sequence or particular protein is very challenging due to a limited number of modifications in such restricted molecule size. Quite often, small modifications in ligand structure lead to a change of target preference, for instance from DNA-targeting to protein-targeting molecule. Scheme 1. Aggregation-prone dye interacting with various targets and reporting interaction with each target by sensitive and bio- applicable spectrometric method. One of our research interests deals with the generally under-investigated approach: exploitation of intrinsic property of some ligands for aggregation, whereby monomeric and aggregated ligand differ strongly not only in target recognition but also in spectroscopic properties. Thus, one ligand molecule could bind with similar affinity to several targets (DNA, RNA, protein)1 giving different spectroscopic responses for each target: to some polynucleotide sequence ligand would bind as monomer, to another sequence as dimer, and protein binding site would again result in spectroscopic response differing from DNA/RNA signal (Scheme 1). The ongoing research endeavors to establish for the low molecular weight ligands the structure-activity guidelines for the fine-tuning of DNA - RNA - protein preferences combined with a recognition by a complementary set of sensitive and bio- applicable spectrometric methods (fluorescence and CD/LD spectrophotometry). References: [1] Ž. Ban, S. Griesbeck, S. Tomić, J. Nitsch, T. Marder, I Piantanida, Chem. Eur. J. (2019) doi.org/10.1002/chem.201903936 ; T. Šmidlehner, M. Badovinac, I. Piantanida, , New J. Chem. 42, (2018), 6655 ; Crnolatac et al, Anal. Chim. Acta 2016, 940, 128 ; L.-M. Tumir et al, Chem., Eur. J. 2012, 18, 3859.

DNA ; RNA ; protein ; sensor, dye, fluorescence

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