McKenzie Luke K, Flamme Marie, Felder Patrick S, Karges Johannes, Bonhomme Frederic, Gandioso Albert, Malosse Christian, Gasser Gilles, Hollenstein Marcel
Institut Pasteur, Department of Structural Biology and Chemistry, Laboratory for Bioorganic Chemistry of Nucleic Acids, CNRS UMR3523 28 rue du Docteur Roux 75724 Paris Cedex 15 France
Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology 75005 Paris France
RSC Chem Biol. 2021 Nov 2;3(1):85-95. doi: 10.1039/d1cb00146a. eCollection 2022 Jan 5.
Ruthenium complexes have emerged as a promising class of compounds for use as photosensitizers (PSs) in photodynamic therapy (PDT) due to their attractive photophysical properties and relative ease of chemical alteration. While promising, they generally are not inherently targeting to disease sites and may therefore be prone to side effects and require higher doses. Aptamers are short oligonucleotides that bind specific targets with high affinity. One such aptamer is AS1411, a nucleolin targeting, G-quadruplex forming, DNA aptamer. Here we present the first example of direct conjugation of a Ru(ii) polypyridyl complex-based PS to an aptamer and an assessment of its cancer cell specific photosensitization including discussion of the challenges faced.
钌配合物因其具有吸引人的光物理性质以及相对易于进行化学修饰,已成为光动力疗法(PDT)中用作光敏剂(PSs)的一类有前景的化合物。尽管前景广阔,但它们通常并非天然靶向疾病部位,因此可能易于产生副作用且需要更高剂量。适体是能与特定靶标高亲和力结合的短寡核苷酸。其中一种适体是AS1411,一种靶向核仁素、形成G-四链体的DNA适体。在此,我们展示了基于钌(II)多吡啶配合物的光敏剂与适体直接偶联的首个实例,并对其癌细胞特异性光致敏作用进行了评估,包括对所面临挑战的讨论。