化学
谷氨酸羧肽酶Ⅱ
谷氨酸受体
羧肽酶
配体(生物化学)
羧肽酶A
抗原
生物化学
内科学
酶
免疫学
受体
医学
生物
癌症
前列腺
作者
Marco Müller,Laura Lucaroni,Nicholas Favalli,Gabriele Bassi,Dario Neri,Samuele Cazzamalli,Sebastian Oehler
标识
DOI:10.1021/acs.jmedchem.4c00332
摘要
Prostate-specific membrane antigen (PSMA)-targeted radio ligand therapeutics (RLTs), such as [177Lu]Lu-PSMA-617 (Pluvicto), have been shown to accumulate in salivary glands and kidneys, potentially leading to undesired side effects. As unwanted accumulation in normal organs may derive from the cross-reactivity of PSMA ligands to glutamate carboxypeptidase III (GCPIII), it may be convenient to block this interaction with GCPIII-selective ligands. Parallel screening of a DNA-encoded chemical library (DEL) against GCPIII and PSMA allowed the identification of GCPIII binders. Structure–activity relationship (SAR) studies resulted in the identification of nanomolar GCPIII ligands with up to 1000-fold selectivity over PSMA. We studied the ability of GCPIII ligands to counteract the binding of [177Lu]Lu-PSMA-617 to human salivary glands by autoradiography and could demonstrate a partial radioprotection.
科研通智能强力驱动
Strongly Powered by AbleSci AI