Natural Product Proteomining, a Quantitative Proteomics Platform, Allows Rapid Discovery of Biosynthetic Gene Clusters for Different Classes of Natural Products
Jacob Gubbens
1
,
Hua Zhu
2
,
Genevieve Girard
2
,
Lijiang Song
3
,
Bogdan I. Florea
1
,
Philip Aston
3
,
Koji Ichinose
4
,
Dmitri V. Filippov
1
,
Young H Choi
2
,
Hermen S. Overkleeft
1
,
Gilles P. van Wezel
2
Publication type: Journal Article
Publication date: 2014-06-01
PubMed ID:
24816229
Drug Discovery
Biochemistry
Molecular Biology
General Medicine
Pharmacology
Clinical Biochemistry
Molecular Medicine
Abstract
Information on gene clusters for natural product biosynthesis is accumulating rapidly because of the current boom of available genome sequencing data. However, linking a natural product to a specific gene cluster remains challenging. Here, we present a widely applicable strategy for the identification of gene clusters for specific natural products, which we name natural product proteomining. The method is based on using fluctuating growth conditions that ensure differential biosynthesis of the bioactivity of interest. Subsequent combination of metabolomics and quantitative proteomics establishes correlations between abundance of natural products and concomitant changes in the protein pool, which allows identification of the relevant biosynthetic gene cluster. We used this approach to elucidate gene clusters for different natural products in Bacillus and Streptomyces, including a novel juglomycin-type antibiotic. Natural product proteomining does not require prior knowledge of the gene cluster or secondary metabolite and therefore represents a general strategy for identification of all types of gene clusters.
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56
Total citations:
56
Citations from 2025:
3
(5.36%)
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GOST
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Gubbens J. et al. Natural Product Proteomining, a Quantitative Proteomics Platform, Allows Rapid Discovery of Biosynthetic Gene Clusters for Different Classes of Natural Products // Chemistry & Biology. 2014. Vol. 21. No. 6. pp. 707-718.
GOST all authors (up to 50)
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Gubbens J., Zhu H., Girard G., Song L., Florea B. I., Aston P., Ichinose K., Filippov D. V., Choi Y. H., Overkleeft H. S., Challis G. L., van Wezel G. P. Natural Product Proteomining, a Quantitative Proteomics Platform, Allows Rapid Discovery of Biosynthetic Gene Clusters for Different Classes of Natural Products // Chemistry & Biology. 2014. Vol. 21. No. 6. pp. 707-718.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.chembiol.2014.03.011
UR - https://doi.org/10.1016/j.chembiol.2014.03.011
TI - Natural Product Proteomining, a Quantitative Proteomics Platform, Allows Rapid Discovery of Biosynthetic Gene Clusters for Different Classes of Natural Products
T2 - Chemistry & Biology
AU - Gubbens, Jacob
AU - Zhu, Hua
AU - Girard, Genevieve
AU - Song, Lijiang
AU - Florea, Bogdan I.
AU - Aston, Philip
AU - Ichinose, Koji
AU - Filippov, Dmitri V.
AU - Choi, Young H
AU - Overkleeft, Hermen S.
AU - Challis, Gregory L.
AU - van Wezel, Gilles P.
PY - 2014
DA - 2014/06/01
PB - Elsevier
SP - 707-718
IS - 6
VL - 21
PMID - 24816229
SN - 1074-5521
SN - 1879-1301
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2014_Gubbens,
author = {Jacob Gubbens and Hua Zhu and Genevieve Girard and Lijiang Song and Bogdan I. Florea and Philip Aston and Koji Ichinose and Dmitri V. Filippov and Young H Choi and Hermen S. Overkleeft and Gregory L. Challis and Gilles P. van Wezel},
title = {Natural Product Proteomining, a Quantitative Proteomics Platform, Allows Rapid Discovery of Biosynthetic Gene Clusters for Different Classes of Natural Products},
journal = {Chemistry & Biology},
year = {2014},
volume = {21},
publisher = {Elsevier},
month = {jun},
url = {https://doi.org/10.1016/j.chembiol.2014.03.011},
number = {6},
pages = {707--718},
doi = {10.1016/j.chembiol.2014.03.011}
}
Cite this
MLA
Copy
Gubbens, Jacob, et al. “Natural Product Proteomining, a Quantitative Proteomics Platform, Allows Rapid Discovery of Biosynthetic Gene Clusters for Different Classes of Natural Products.” Chemistry & Biology, vol. 21, no. 6, Jun. 2014, pp. 707-718. https://doi.org/10.1016/j.chembiol.2014.03.011.