Challenges in observing transcription–translation for bottom-up synthetic biology

Synthetic biology aims to create a viable synthetic cell. However, to achieve this goal, it is essential first to gain a profound understanding of the cellular systems used to build that cell, how to reconstitute those systems in the compartments, and how to track their function. Transcription and t...

Full description

Saved in:
Bibliographic Details
Main Authors: Vadim G. Bogatyr, Gijs J. L. Wuite
Format: Article
Language:English
Published: Cambridge University Press 2025-01-01
Series:QRB Discovery
Subjects:
Online Access:https://www.cambridge.org/core/product/identifier/S2633289224000279/type/journal_article
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832583707561558016
author Vadim G. Bogatyr
Gijs J. L. Wuite
author_facet Vadim G. Bogatyr
Gijs J. L. Wuite
author_sort Vadim G. Bogatyr
collection DOAJ
description Synthetic biology aims to create a viable synthetic cell. However, to achieve this goal, it is essential first to gain a profound understanding of the cellular systems used to build that cell, how to reconstitute those systems in the compartments, and how to track their function. Transcription and translation are two vital cellular systems responsible for the production of RNA and, consequently, proteins, without which the cell would not be able to maintain itself or fulfill its functions. This review discusses in detail how the Protein synthesis Using Recombinant Element (PURE) system and cell lysate are used to reconstitute transcription–translation in vitro. Furthermore, it examines how these systems can be encapsulated in GUVs using the existing methods. It also assesses approaches available to image transcription and translation with a diverse arsenal of fluorescence microscopy techniques and a broad collection of probes developed in recent decades. Finally, it highlights solutions for the challenge ahead, namely the decoupling of the two systems in PURE, and discusses the prospects of synthetic biology in the modern world.
format Article
id doaj-art-32367031bcb74e9aa64b95d0c2473d37
institution Kabale University
issn 2633-2892
language English
publishDate 2025-01-01
publisher Cambridge University Press
record_format Article
series QRB Discovery
spelling doaj-art-32367031bcb74e9aa64b95d0c2473d372025-01-28T08:01:13ZengCambridge University PressQRB Discovery2633-28922025-01-01610.1017/qrd.2024.27Challenges in observing transcription–translation for bottom-up synthetic biologyVadim G. Bogatyr0https://orcid.org/0000-0002-2829-3197Gijs J. L. Wuite1https://orcid.org/0000-0002-5706-043XDepartment of Physics and Astronomy and LaserLab, Faculty of Science, Vrije Universiteit, Amsterdam, NetherlandsDepartment of Physics and Astronomy and LaserLab, Faculty of Science, Vrije Universiteit, Amsterdam, NetherlandsSynthetic biology aims to create a viable synthetic cell. However, to achieve this goal, it is essential first to gain a profound understanding of the cellular systems used to build that cell, how to reconstitute those systems in the compartments, and how to track their function. Transcription and translation are two vital cellular systems responsible for the production of RNA and, consequently, proteins, without which the cell would not be able to maintain itself or fulfill its functions. This review discusses in detail how the Protein synthesis Using Recombinant Element (PURE) system and cell lysate are used to reconstitute transcription–translation in vitro. Furthermore, it examines how these systems can be encapsulated in GUVs using the existing methods. It also assesses approaches available to image transcription and translation with a diverse arsenal of fluorescence microscopy techniques and a broad collection of probes developed in recent decades. Finally, it highlights solutions for the challenge ahead, namely the decoupling of the two systems in PURE, and discusses the prospects of synthetic biology in the modern world.https://www.cambridge.org/core/product/identifier/S2633289224000279/type/journal_articleDNAtranscritpionfluorescenceRNAprotein–nucleic acid interactionstranslationsynthetic biology
spellingShingle Vadim G. Bogatyr
Gijs J. L. Wuite
Challenges in observing transcription–translation for bottom-up synthetic biology
QRB Discovery
DNA
transcritpion
fluorescence
RNA
protein–nucleic acid interactions
translation
synthetic biology
title Challenges in observing transcription–translation for bottom-up synthetic biology
title_full Challenges in observing transcription–translation for bottom-up synthetic biology
title_fullStr Challenges in observing transcription–translation for bottom-up synthetic biology
title_full_unstemmed Challenges in observing transcription–translation for bottom-up synthetic biology
title_short Challenges in observing transcription–translation for bottom-up synthetic biology
title_sort challenges in observing transcription translation for bottom up synthetic biology
topic DNA
transcritpion
fluorescence
RNA
protein–nucleic acid interactions
translation
synthetic biology
url https://www.cambridge.org/core/product/identifier/S2633289224000279/type/journal_article
work_keys_str_mv AT vadimgbogatyr challengesinobservingtranscriptiontranslationforbottomupsyntheticbiology
AT gijsjlwuite challengesinobservingtranscriptiontranslationforbottomupsyntheticbiology