Luma Larita, Pursteiner Judith C, Fischer Tobias, Hegger Rainer, Burghardt Irene, Wachtveitl Josef, Heckel Alexander
Goethe University Frankfurt, Institute for Organic Chemistry and Chemical Biology Max-von-Laue-Str. 7 60438 Frankfurt Germany
Goethe University Frankfurt, Institute for Physical and Theoretical Chemistry Max-von-Laue-Str. 7 60438 Frankfurt Germany
Chem Sci. 2024 Sep 4;15(38):15783-9. doi: 10.1039/d4sc05175k.
Fluorescence quenchers for application in DNA - like the BHQ family - tend to be large molecules which need to be attached, often post-synthetically, long linkers. In this study, we present two new iminothioindoxyl--nucleosidic quenchers which are very compact, feature a native backbone and can be introduced into DNA regular solid-phase synthesis. Especially with d as juxtaposed nucleobase, they have a defined location and orientation in a DNA duplex with minimal perturbation of the structure and hence interaction capabilities. Depending on the nature of the fluorophore, they can be used for orientation-(un)specific FRET studies. Their Förster radius is smaller than the one of BHQ-2. This makes these quenchers ideal for sophisticated studies using conditional quenching in the range between 470 and 670 nm in DNA.
用于DNA的荧光猝灭剂——如BHQ家族——往往是大分子,通常需要在合成后通过长连接子连接。在本研究中,我们展示了两种新型亚氨基硫代吲哚 - 核苷猝灭剂,它们非常紧凑,具有天然主链,并且可以通过常规固相合成引入到DNA中。特别是当d作为相邻的核碱基时,它们在DNA双链体中具有明确的位置和取向,对结构的扰动最小,因此具有相互作用能力。根据荧光团的性质,它们可用于定向(非)特异性荧光共振能量转移(FRET)研究。它们的福斯特半径小于BHQ-2的福斯特半径。这使得这些猝灭剂非常适合在DNA中470至670nm范围内使用条件猝灭进行的复杂研究。