Das Poulomi, Phan Anh Tuân
School of Physical and Mathematical Sciences, Nanyang Technological University, 637371, Singapore.
NTU Institute of Structural Biology, Nanyang Technological University, 636921, Singapore.
Chem Commun (Camb). 2022 Oct 6;58(80):11264-11267. doi: 10.1039/d2cc03374g.
G-quadruplexes (G4s) are attractive anticancer targets. While right-handed G4s have been extensively investigated with many specific ligands reported, left-handed G4s formed by natural DNA have been recently discovered. Here we show that ligands specific for right-handed G4s, such as Phen-DC and RHAU peptide, do not bind specifically to left-handed G4s. In right-handed G4s, these ligands can displace capping overhangs and/or loops to stack on the exposed terminal tetrads. In contrast, the presence of tight T-capping in left-handed G4s hinders access to the tetrads.
G-四链体(G4s)是颇具吸引力的抗癌靶点。虽然右手性G4s已得到广泛研究,并有许多特异性配体被报道,但由天然DNA形成的左手性G4s最近才被发现。在此我们表明,针对右手性G4s的特异性配体,如Phen-DC和RHAU肽,不会特异性结合左手性G4s。在右手性G4s中,这些配体可以取代封端突出端和/或环,从而堆叠在暴露的末端四分体上。相比之下,左手性G4s中紧密的T封端的存在阻碍了对四分体的接近。