Fisher Martin J, Williamson Daniel J, Burslem George M, Plante Jeffrey P, Manfield Iain W, Tiede Christian, Ault James R, Stockley Peter G, Plein Sven, Maqbool Azhar, Tomlinson Darren C, Foster Richard, Warriner Stuart L, Bon Robin S
School of Chemistry , University of Leeds , LS2 9JT , UK . Email:
Astbury Centre for Structural Molecular Biology , University of Leeds , UK ; School of Molecular and Cellular Biology , University of Leeds , UK.
RSC Adv. 2015 Dec 9;5(116):96194-96200. doi: 10.1039/c5ra20359g. Epub 2015 Nov 11.
The development of novel protein-targeted MRI contrast agents crucially depends on the ability to derivatise suitable targeting moieties with a high payload of relaxation enhancer (, gadolinium(iii) complexes such as Gd-DOTA), without losing affinity for the target proteins. Here, we report robust synthetic procedures for the preparation of trivalent Gd-DOTA reagents with various chemical handles for site-specific modification of biomolecules. The reagents were shown to successfully label proteins through isothiocyanate ligation or through site-specific thiol-maleimide ligation and strain-promoted azide-alkyne cycloaddition.
新型蛋白质靶向磁共振成像(MRI)造影剂的开发关键取决于能否用高负载量的弛豫增强剂(如钆(III)配合物Gd-DOTA)对合适的靶向部分进行衍生化,同时又不丧失对靶蛋白的亲和力。在此,我们报告了用于制备具有各种化学手柄的三价Gd-DOTA试剂的稳健合成程序,这些手柄可用于生物分子的位点特异性修饰。这些试剂已证明可通过异硫氰酸酯连接、位点特异性硫醇-马来酰亚胺连接以及应变促进的叠氮化物-炔烃环加成成功标记蛋白质。