Inferring structure factors of weakly populated excited states in perturbative crystallography experiments

Perturbative X-ray crystallography can visualize functional dynamics and conformational changes in proteins at atomic resolution. During a typical perturbative crystallography experiment, only a fraction of protein molecules in a crystal will be perturbed, or "excited". As a result, the observed data represent a mixture of excited and ground states. The conventional approach to estimating the excited-state structure factor amplitudes is to linearly extrapolate the difference between the structure factor amplitudes of the perturbed and unperturbed data. This approach often fails to yield well-refined structural models because it amplifies experimental errors and neglects phase differences between the ground and excited states. Here, we introduce an approach to estimating excited-state structure factor amplitudes that starts from a statistical prior for the correlations between excited and ground states. Using benchmarks from time-resolved crystallography and a drug-fragment screen, we illustrate how this approach effectively addresses the limitations of traditional extrapolation.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-04-21
DOI
https://doi.org/10.64898/2026.04.16.719053
Primary Topic
Enzyme Structure and Function
Type
article
Field-Weighted Citation Impact
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article

Inferring structure factors of weakly populated excited states in perturbative crystallography experiments

H Wang, Doeke Romke Hekstra, Andrew K. Choe
bioRxiv (Cold Spring Harbor Laboratory)
Enzyme Structure and Function
article

Inferring structure factors of weakly populated excited states in perturbative crystallography experiments

H Wang, Doeke Romke Hekstra, Andrew K. Choe
article en

Abstract

Perturbative X-ray crystallography can visualize functional dynamics and conformational changes in proteins at atomic resolution. During a typical perturbative crystallography experiment, only a fraction of protein molecules in a crystal will be perturbed, or "excited". As a result, the observed data represent a mixture of excited and ground states. The conventional approach to estimating the excited-state structure factor amplitudes is to linearly extrapolate the difference between the structure factor amplitudes of the perturbed and unperturbed data. This approach often fails to yield well-refined structural models because it amplifies experimental errors and neglects phase differences between the ground and excited states. Here, we introduce an approach to estimating excited-state structure factor amplitudes that starts from a statistical prior for the correlations between excited and ground states. Using benchmarks from time-resolved crystallography and a drug-fragment screen, we illustrate how this approach effectively addresses the limitations of traditional extrapolation.

bioRxiv (Cold Spring Harbor Laboratory)
Harvard University (US)
Openalex Percentile: Top 18%
Enzyme Structure and Function
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Inferring structure factors of weakly populated excited states in perturbative crystallography experiments — H Wang, Doeke Romke Hekstra, et al. · bioRxiv (Cold Spring Harbor Laboratory) (2026) | TGRS Research Map | TGRS