Comparative differential cuproproteomes of Rhodobacter capsulatus reveal novel copper homeostasis related proteins. Issue 4 (9th March 2020)
- Record Type:
- Journal Article
- Title:
- Comparative differential cuproproteomes of Rhodobacter capsulatus reveal novel copper homeostasis related proteins. Issue 4 (9th March 2020)
- Main Title:
- Comparative differential cuproproteomes of Rhodobacter capsulatus reveal novel copper homeostasis related proteins
- Authors:
- Selamoglu, Nur
Önder, Özlem
Öztürk, Yavuz
Khalfaoui-Hassani, Bahia
Blaby-Haas, Crysten E.
Garcia, Benjamin A.
Koch, Hans-Georg
Daldal, Fevzi - Abstract:
- Abstract : Cuproproteome of model bacterium Rhodobacter capsulatus reveals 75 Cu-responsive proteins that are strongly influenced (2–300 fold) by Cu availability. Abstract : Copper (Cu) is an essential, but toxic, micronutrient for living organisms and cells have developed sophisticated response mechanisms towards both the lack and the excess of Cu in their environments. In this study, we achieved a global view of Cu-responsive changes in the prokaryotic model organism Rhodobacter capsulatus using label-free quantitative differential proteomics. Semi-aerobically grown cells under heterotrophic conditions in minimal medium (∼0.3 μM Cu) were compared with cells supplemented with either 5 μM Cu or with 5 mM of the Cu-chelator bathocuproine sulfonate. Mass spectrometry based bottom-up proteomics of unfractionated cell lysates identified 2430 of the 3632 putative proteins encoded by the genome, producing a robust proteome dataset for R. capsulatus . Use of biological and technical replicates for each growth condition yielded high reproducibility and reliable quantification for 1926 of the identified proteins. Comparison of cells grown under Cu-excess or Cu-depleted conditions to those grown under minimal Cu-sufficient conditions revealed that 75 proteins exhibited statistically significant ( p < 0.05) abundance changes, ranging from 2- to 300-fold. A subset of the highly Cu-responsive proteins was orthogonally probed using molecular genetics, validating that several of them wereAbstract : Cuproproteome of model bacterium Rhodobacter capsulatus reveals 75 Cu-responsive proteins that are strongly influenced (2–300 fold) by Cu availability. Abstract : Copper (Cu) is an essential, but toxic, micronutrient for living organisms and cells have developed sophisticated response mechanisms towards both the lack and the excess of Cu in their environments. In this study, we achieved a global view of Cu-responsive changes in the prokaryotic model organism Rhodobacter capsulatus using label-free quantitative differential proteomics. Semi-aerobically grown cells under heterotrophic conditions in minimal medium (∼0.3 μM Cu) were compared with cells supplemented with either 5 μM Cu or with 5 mM of the Cu-chelator bathocuproine sulfonate. Mass spectrometry based bottom-up proteomics of unfractionated cell lysates identified 2430 of the 3632 putative proteins encoded by the genome, producing a robust proteome dataset for R. capsulatus . Use of biological and technical replicates for each growth condition yielded high reproducibility and reliable quantification for 1926 of the identified proteins. Comparison of cells grown under Cu-excess or Cu-depleted conditions to those grown under minimal Cu-sufficient conditions revealed that 75 proteins exhibited statistically significant ( p < 0.05) abundance changes, ranging from 2- to 300-fold. A subset of the highly Cu-responsive proteins was orthogonally probed using molecular genetics, validating that several of them were indeed involved in cellular Cu homeostasis. … (more)
- Is Part Of:
- Metallomics. Volume 12:Issue 4(2020)
- Journal:
- Metallomics
- Issue:
- Volume 12:Issue 4(2020)
- Issue Display:
- Volume 12, Issue 4 (2020)
- Year:
- 2020
- Volume:
- 12
- Issue:
- 4
- Issue Sort Value:
- 2020-0012-0004-0000
- Page Start:
- 572
- Page End:
- 591
- Publication Date:
- 2020-03-09
- Subjects:
- Metals -- Physiological effect -- Periodicals
572.51 - Journal URLs:
- https://academic.oup.com/metallomics/issue ↗
http://www.rsc.org/ ↗
http://www.rsc.org/Publishing/Journals/mt/index.asp ↗ - DOI:
- 10.1039/c9mt00314b ↗
- Languages:
- English
- ISSNs:
- 1756-5901
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5694.710000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13835.xml