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Real-Time Measurement of Protein Crystal Growth Rates within the Microfluidic Device to Understand the Microspace Effect
[Image: see text] Preparation of high-quality protein crystals is a major challenge in protein crystallography. Natural convection is considered to be an uncontrollable factor of the crystallization process at the ground level as it disturbs the concentration gradient around the growing crystal, res...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376889/ https://www.ncbi.nlm.nih.gov/pubmed/32715205 http://dx.doi.org/10.1021/acsomega.0c01285 |
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author | Maeki, Masatoshi Yamazaki, Shohei Takeda, Reo Ishida, Akihiko Tani, Hirofumi Tokeshi, Manabu |
author_facet | Maeki, Masatoshi Yamazaki, Shohei Takeda, Reo Ishida, Akihiko Tani, Hirofumi Tokeshi, Manabu |
author_sort | Maeki, Masatoshi |
collection | PubMed |
description | [Image: see text] Preparation of high-quality protein crystals is a major challenge in protein crystallography. Natural convection is considered to be an uncontrollable factor of the crystallization process at the ground level as it disturbs the concentration gradient around the growing crystal, resulting in lower-quality crystals. A microfluidic environment expects an imitated microgravity environment because of the small Gr number. However, the mechanism of protein crystal growth in the microfluidic device was not elucidated due to limitations in measuring the crystal growth process within the device. Here, we demonstrate the real-time measurement of protein crystal growth rates within the microfluidic devices by laser confocal microscopy with differential interference contrast microscopy (LCM-DIM) at the nanometer scale. We confirmed the normal growth rates in the 20 and 30 μm-deep microfluidic device to be 42.2 and 536 nm/min, respectively. In addition, the growth rate of crystals in the 20 μm-deep microfluidic device was almost the same as that reported in microgravity conditions. This phenomenon may enable the development of more accessible alternatives to the microgravity environment of the International Space Station. |
format | Online Article Text |
id | pubmed-7376889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73768892020-07-24 Real-Time Measurement of Protein Crystal Growth Rates within the Microfluidic Device to Understand the Microspace Effect Maeki, Masatoshi Yamazaki, Shohei Takeda, Reo Ishida, Akihiko Tani, Hirofumi Tokeshi, Manabu ACS Omega [Image: see text] Preparation of high-quality protein crystals is a major challenge in protein crystallography. Natural convection is considered to be an uncontrollable factor of the crystallization process at the ground level as it disturbs the concentration gradient around the growing crystal, resulting in lower-quality crystals. A microfluidic environment expects an imitated microgravity environment because of the small Gr number. However, the mechanism of protein crystal growth in the microfluidic device was not elucidated due to limitations in measuring the crystal growth process within the device. Here, we demonstrate the real-time measurement of protein crystal growth rates within the microfluidic devices by laser confocal microscopy with differential interference contrast microscopy (LCM-DIM) at the nanometer scale. We confirmed the normal growth rates in the 20 and 30 μm-deep microfluidic device to be 42.2 and 536 nm/min, respectively. In addition, the growth rate of crystals in the 20 μm-deep microfluidic device was almost the same as that reported in microgravity conditions. This phenomenon may enable the development of more accessible alternatives to the microgravity environment of the International Space Station. American Chemical Society 2020-07-08 /pmc/articles/PMC7376889/ /pubmed/32715205 http://dx.doi.org/10.1021/acsomega.0c01285 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Maeki, Masatoshi Yamazaki, Shohei Takeda, Reo Ishida, Akihiko Tani, Hirofumi Tokeshi, Manabu Real-Time Measurement of Protein Crystal Growth Rates within the Microfluidic Device to Understand the Microspace Effect |
title | Real-Time Measurement of Protein Crystal Growth Rates
within the Microfluidic Device to Understand the Microspace Effect |
title_full | Real-Time Measurement of Protein Crystal Growth Rates
within the Microfluidic Device to Understand the Microspace Effect |
title_fullStr | Real-Time Measurement of Protein Crystal Growth Rates
within the Microfluidic Device to Understand the Microspace Effect |
title_full_unstemmed | Real-Time Measurement of Protein Crystal Growth Rates
within the Microfluidic Device to Understand the Microspace Effect |
title_short | Real-Time Measurement of Protein Crystal Growth Rates
within the Microfluidic Device to Understand the Microspace Effect |
title_sort | real-time measurement of protein crystal growth rates
within the microfluidic device to understand the microspace effect |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376889/ https://www.ncbi.nlm.nih.gov/pubmed/32715205 http://dx.doi.org/10.1021/acsomega.0c01285 |
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