Dissecting the Ultrafast Stepwise Bidirectional Proton Relay in a Blue-Light Photoreceptor

Proton relays through H-bond networks are essential in realizing the functionality of protein machines such as in photosynthesis and photoreceptors. It has been challenging to dissect the rates and energetics of individual proton-transfer steps during the proton relay. Here, we have designed a proton rocking blue light using a flavin (BLUF) domain with the flavin mononucleotide (FMN)-glutamic acid (E)-tryptophan (W) triad and have resolved the four individual proton-transfer steps kinetically using ultrafast spectroscopy. We have found that after the photo-induced charge separation forming FMN center dot-/E-COOH/ WH center dot+, the proton first rapidly jumps from the bridging E-COOH to FMN- (TfPT2 = 3.8 ps; KIE = 1.0), followed by a second proton transfer from WH center dot+ to E-COO- (TfPT1 = 336 ps; KIE = 2.6) which immediately rocks back to W center dot(TrPT1 = 85 ps; KIE = 6.7), followed by a proton return from FMNH center dot to E-COO- (TrPT2 = 34 ps; KIE = 3.3) with the final charge recombination between FMN center dot- and WH center dot+ to close the reaction cycle. Our results revisited the Grotthuss mechanism on the ultrafast timescale using the BLUF domain as a paradigm protein.

Automated summary

Proton relays through H-bond networks are crucial in protein machines. In this study, we designed a proton rocking blue light and used ultrafast spectroscopy to analyze the individual proton-transfer steps. We found that the proton jumps from E-COOH to FMN- rapidly, followed by a second proton transfer from WH+ to E-COO-, which immediately rocks back to W•. Our findings provide insights into the Grotthuss mechanism on the ultrafast timescale.