Abstract Tris NTA chelators consist of three metal‐chelating N‐nitrilotriacetic acids (NTAs) connected by a scaffold structure. Coupled to a fluorophore or other reporter, tris NTAs can be used as a probe for live‐cell labeling of histidine‐tagged proteins. In their Communication (DOI: 10.1002/anie.201802746), R. Tampé et al. report large differences in affinity and stability between linear, dendritic, and cyclic scaffolds, and clarify which trisNTA scaffold is superior for in vitro and cellular applications.
CITATION STYLE
Gatterdam, K., Joest, E. F., Gatterdam, V., & Tampé, R. (2018). Back Cover: The Scaffold Design of Trivalent Chelator Heads Dictates Affinity and Stability for Labeling His‐tagged Proteins in vitro and in Cells (Angew. Chem. Int. Ed. 38/2018). Angewandte Chemie International Edition, 57(38), 12586–12586. https://doi.org/10.1002/anie.201808284
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