Citation
Yang, Chien-I (2023) Mechanism and Function of Nascent Protein Modification in Bacteria. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/qhz7-a383. https://resolver.caltech.edu/CaltechTHESIS:07032022-182356199
Abstract
Newly synthesized proteins undergo multiple modifications to ensure proper biogenesis and acquire their functions. N-terminal methionine excision (NME), mediated by the sequential actions of peptide deformylase (PDF) and methionine aminopeptidase (MAP), is an essential and the most prevalent N-terminal protein modification in the bacterial proteome. Despite the extensive studies on enzymatic catalysis, how NME impacts various cellular functions and how the enzymes achieve timing and selectivity under complex cellular conditions have been long-standing puzzles.
In this work, we use a combination of biochemical analyses, computational modeling, and in vivo measurements to investigate the molecular mechanisms and physiological functions of cotranslational NME reactions. We show that the interactions between the ribosome, the nascent chain, the NME enzymes, and other ribosome-associated protein biogenesis factors dramatically remodel the kinetics and specificity of NME reactions under physiological conditions. In addition, we apply time-resolved, system-wide analyses on the translatome and steady-state proteome to study how the inhibition of PDF influences diverse cellular pathways in bacteria. The results unveil the impact of NME on the biogenesis of nascent proteins and highlight the role of the membrane in coupling the biochemical activities of NME enzymes to cellular physiology.
Item Type: | Thesis (Dissertation (Ph.D.)) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Subject Keywords: | protein biogenesis; N-terminal protein modification; peptide deformylase; methionine aminopeptidase; ribosome | |||||||||
Degree Grantor: | California Institute of Technology | |||||||||
Division: | Chemistry and Chemical Engineering | |||||||||
Major Option: | Chemistry | |||||||||
Thesis Availability: | Public (worldwide access) | |||||||||
Research Advisor(s): |
| |||||||||
Thesis Committee: |
| |||||||||
Defense Date: | 28 June 2022 | |||||||||
Funders: |
| |||||||||
Record Number: | CaltechTHESIS:07032022-182356199 | |||||||||
Persistent URL: | https://resolver.caltech.edu/CaltechTHESIS:07032022-182356199 | |||||||||
DOI: | 10.7907/qhz7-a383 | |||||||||
Related URLs: |
| |||||||||
ORCID: |
| |||||||||
Default Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | |||||||||
ID Code: | 14966 | |||||||||
Collection: | CaltechTHESIS | |||||||||
Deposited By: | Chien I Yang | |||||||||
Deposited On: | 11 Jul 2022 23:18 | |||||||||
Last Modified: | 18 Jul 2022 19:03 |
Thesis Files
PDF
- Final Version
See Usage Policy. 13MB | |
MS Excel (Dataset 1)
- Supplemental Material
See Usage Policy. 1MB | |
MS Excel (Dataset 2)
- Supplemental Material
See Usage Policy. 72kB | |
MS Excel (Dataset 3)
- Supplemental Material
See Usage Policy. 1MB | |
MS Excel (Dataset 4)
- Supplemental Material
See Usage Policy. 101kB |
Repository Staff Only: item control page