Scaling and merging time-resolved pink-beam diffraction with variational inference
Time-resolved x-ray crystallography (TR-X) at synchrotrons and free electron lasers is a promising technique for recording dynamics of molecules at atomic resolution. While experimental methods for TR-X have proliferated and matured, data analysis is often difficult. Extracting small, time-dependent...
| Published in: | Structural Dynamics |
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| Main Authors: | , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
AIP Publishing LLC and ACA
2024-11-01
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| Online Access: | http://dx.doi.org/10.1063/4.0000269 |
| _version_ | 1850031187100172288 |
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| author | Kara A. Zielinski Cole Dolamore Harrison K. Wang Robert W. Henning Mark A. Wilson Lois Pollack Vukica Srajer Doeke R. Hekstra Kevin M. Dalton |
| author_facet | Kara A. Zielinski Cole Dolamore Harrison K. Wang Robert W. Henning Mark A. Wilson Lois Pollack Vukica Srajer Doeke R. Hekstra Kevin M. Dalton |
| author_sort | Kara A. Zielinski |
| collection | DOAJ |
| container_title | Structural Dynamics |
| description | Time-resolved x-ray crystallography (TR-X) at synchrotrons and free electron lasers is a promising technique for recording dynamics of molecules at atomic resolution. While experimental methods for TR-X have proliferated and matured, data analysis is often difficult. Extracting small, time-dependent changes in signal is frequently a bottleneck for practitioners. Recent work demonstrated this challenge can be addressed when merging redundant observations by a statistical technique known as variational inference (VI). However, the variational approach to time-resolved data analysis requires identification of successful hyperparameters in order to optimally extract signal. In this case study, we present a successful application of VI to time-resolved changes in an enzyme, DJ-1, upon mixing with a substrate molecule, methylglyoxal. We present a strategy to extract high signal-to-noise changes in electron density from these data. Furthermore, we conduct an ablation study, in which we systematically remove one hyperparameter at a time to demonstrate the impact of each hyperparameter choice on the success of our model. We expect this case study will serve as a practical example for how others may deploy VI in order to analyze their time-resolved diffraction data. |
| format | Article |
| id | doaj-art-26fadbc3cda74feda7fe75f2e7c1c829 |
| institution | Directory of Open Access Journals |
| issn | 2329-7778 |
| language | English |
| publishDate | 2024-11-01 |
| publisher | AIP Publishing LLC and ACA |
| record_format | Article |
| spelling | doaj-art-26fadbc3cda74feda7fe75f2e7c1c8292025-08-20T00:35:57ZengAIP Publishing LLC and ACAStructural Dynamics2329-77782024-11-01116064301064301-1310.1063/4.0000269Scaling and merging time-resolved pink-beam diffraction with variational inferenceKara A. Zielinski0Cole Dolamore1Harrison K. Wang2Robert W. Henning3Mark A. Wilson4Lois Pollack5Vukica Srajer6Doeke R. Hekstra7Kevin M. Dalton8 School of Applied and Engineering Physics, Cornell University, Ithaca, New York 14853, USA Department of Biochemistry and the Redox Biology Center, University of Nebraska, Lincoln, Nebraska 68588, USA Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA BioCARS, Center for Advanced Radiation Sources, The University of Chicago, Lemont, Illinois 60439, USA Department of Biochemistry and the Redox Biology Center, University of Nebraska, Lincoln, Nebraska 68588, USA School of Applied and Engineering Physics, Cornell University, Ithaca, New York 14853, USA BioCARS, Center for Advanced Radiation Sources, The University of Chicago, Lemont, Illinois 60439, USA Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USATime-resolved x-ray crystallography (TR-X) at synchrotrons and free electron lasers is a promising technique for recording dynamics of molecules at atomic resolution. While experimental methods for TR-X have proliferated and matured, data analysis is often difficult. Extracting small, time-dependent changes in signal is frequently a bottleneck for practitioners. Recent work demonstrated this challenge can be addressed when merging redundant observations by a statistical technique known as variational inference (VI). However, the variational approach to time-resolved data analysis requires identification of successful hyperparameters in order to optimally extract signal. In this case study, we present a successful application of VI to time-resolved changes in an enzyme, DJ-1, upon mixing with a substrate molecule, methylglyoxal. We present a strategy to extract high signal-to-noise changes in electron density from these data. Furthermore, we conduct an ablation study, in which we systematically remove one hyperparameter at a time to demonstrate the impact of each hyperparameter choice on the success of our model. We expect this case study will serve as a practical example for how others may deploy VI in order to analyze their time-resolved diffraction data.http://dx.doi.org/10.1063/4.0000269 |
| spellingShingle | Kara A. Zielinski Cole Dolamore Harrison K. Wang Robert W. Henning Mark A. Wilson Lois Pollack Vukica Srajer Doeke R. Hekstra Kevin M. Dalton Scaling and merging time-resolved pink-beam diffraction with variational inference |
| title | Scaling and merging time-resolved pink-beam diffraction with variational inference |
| title_full | Scaling and merging time-resolved pink-beam diffraction with variational inference |
| title_fullStr | Scaling and merging time-resolved pink-beam diffraction with variational inference |
| title_full_unstemmed | Scaling and merging time-resolved pink-beam diffraction with variational inference |
| title_short | Scaling and merging time-resolved pink-beam diffraction with variational inference |
| title_sort | scaling and merging time resolved pink beam diffraction with variational inference |
| url | http://dx.doi.org/10.1063/4.0000269 |
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