Dalvit Claudio, Veronesi Marina, Vulpetti Anna
Lavis, Trento, Italy.
D3-PharmaChemistry, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163, Genova, Italy.
J Biomol NMR. 2020 Nov;74(10-11):613-631. doi: 10.1007/s10858-020-00311-3. Epub 2020 Apr 28.
The substrate- or cofactor-based fluorine NMR screening, also known as n-FABS (n fluorine atoms for biochemical screening), represents a powerful method for performing a direct functional assay in the search of inhibitors or enhancers of an enzymatic reaction. Although it suffers from the intrinsic low sensitivity compared to other biophysical techniques usually applied in functional assays, it has some distinctive features that makes it appealing for tackling complex chemical and biological systems. Its strengths are represented by the easy set-up, robustness, flexibility, lack of signal interference and rich information content resulting in the identification of bona fide inhibitors and reliable determination of their inhibitory strength. The versatility of the n-FABS allows its application to either purified enzymes, cell lysates or intact living cells. The principles, along with theoretical, technical and practical aspects, of the methodology are discussed. Furthermore, several applications of the technique to pharmaceutical projects are presented.
基于底物或辅因子的氟核磁共振筛选,也称为n-FABS(用于生化筛选的n个氟原子),是一种在寻找酶促反应抑制剂或增强剂时进行直接功能测定的强大方法。尽管与功能测定中通常使用的其他生物物理技术相比,它具有固有的低灵敏度,但它具有一些独特的特征,使其在处理复杂的化学和生物系统时具有吸引力。其优势在于设置简便、稳健性强、灵活性高、无信号干扰且信息丰富,能够识别真正的抑制剂并可靠地确定其抑制强度。n-FABS的多功能性使其可应用于纯化的酶、细胞裂解物或完整的活细胞。本文讨论了该方法的原理以及理论、技术和实际方面。此外,还介绍了该技术在制药项目中的一些应用。