An improved fluorescent noncanonical amino acid for measuring conformational distributions using time-resolved transition metal ion FRET.

ABSTRACT: With the recent explosion in high-resolution protein structures, one of the next frontiers in biology is elucidating the mechanisms by which conformational rearrangements in proteins are regulated to meet the needs of cells under changing conditions. Rigorously measuring protein energetics and dynamics requires the development of new methods that can resolve structural heterogeneity and conformational distributions. We have previously developed steady-state transition metal ion fluorescence resonance energy transfer (tmFRET) approaches using a fluorescent noncanonical amino acid donor (Anap) and transition metal ion acceptor to probe conformational rearrangements in soluble and membrane proteins. Here, we show that the fluorescent noncanonical amino acid Acd has superior photophysical prop

SUBMITTER: Zagotta WN 

PROVIDER: S-EPMC8500717 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature