Proteomics

Dataset Information

0

OTS Development and E. coli Proteome LC-MSMS


ABSTRACT: Over the past twenty years, the development of orthogonal biological systems has sparked a revolution in our ability to study cellular physiology. Orthogonal translation systems (OTSs) enable site-specific incorporation of hundreds of non-standard amino acids, offering unprecedented access to the study of cellular mechanisms modulated by post-translational modifications (e.g. protein phosphorylation). Although development of phosphoserine-OTSs (pSerOTS) has been significant, little work has focused on the biology of OTS development and utilization. To better understand the impact of OTSs on host physiology, we utilize pSerOTS as a model to systematically explore the extent to which OTS components interact with Escherichia coli. Using this information, we constructed pSerOTS variants designed to enhance OTS orthogonality by minimizing interactions with host processes and decreasing stress response activation. Our expanded understanding of OTS:host interactions enables informed OTS design practices which minimize the negative impact of OTSs while improving OTS performance across a range of experimental settings.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Escherichia Coli

SUBMITTER: Kyle Mohler  

LAB HEAD: Jesse Rinehart

PROVIDER: PXD026217 | Pride | 2023-07-27

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Proteome_Full-OTS-Stress_SEARCH.zip Other
Proteome_OTS-component-stress_SEARCH.zip Other
QX1_19_0664.raw Raw
QX1_19_0666.raw Raw
QX1_19_0668.raw Raw
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Publications

System-wide optimization of an orthogonal translation system with enhanced biological tolerance.

Mohler Kyle K   Moen Jack M JM   Rogulina Svetlana S   Rinehart Jesse J  

Molecular systems biology 20230721 8


Over the past two decades, synthetic biological systems have revolutionized the study of cellular physiology. The ability to site-specifically incorporate biologically relevant non-standard amino acids using orthogonal translation systems (OTSs) has proven particularly useful, providing unparalleled access to cellular mechanisms modulated by post-translational modifications, such as protein phosphorylation. However, despite significant advances in OTS design and function, the systems-level biolo  ...[more]

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