Olivier Pible

Mr. Olivier Pible

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2014 in Journal of Proteomics
Verified
Journal Article
Closed access
Jean ArmengaudJean Armengaud
Jean Armengaud
JTJudith Trapp
Judith Trapp
OPOlivier Pible
Olivier Pible
OGOlivier Geffard
Olivier Geffard
ACArnaud Chaumot
Arnaud Chaumot
EHErica M. Hartmann
Erica M. Hartmann

18 July 2014
Verified
Book Chapter
Closed access
PDF file
EHErica M. Hartmann
Erica M. Hartmann
FAFrançois Allain
François Allain
JGJean-Charles Gaillard
Jean-Charles Gaillard
OPOlivier Pible
Olivier Pible
Jean ArmengaudJean Armengaud
Jean Armengaud

15 December 2021 in Nature Communications
Verified
Journal Article
Open access
PDF file
TBTim Van Den Bossche
Tim Van Den Bossche
BKBenoit J. Kunath
Benoit J. Kunath
KSKay Schallert
Kay Schallert
SSStephanie S. Schäpe
Stephanie S. Schäpe
PAPaul E. Abraham
Paul E. Abraham
TMThilo Muth
Thilo Muth
Metaproteomics has matured into a powerful tool to assess functional interactions in microbial communities. While many metaproteomic workflows are available, the impact of method choice on results remains unclear. Here, we carry out a community-driven, multi-laboratory comparison in metaproteomics: the critical assessment of metaproteome investigation study (CAMPI). Based on well-established workflows, we evaluate the effect of sample preparation, mass spectrometry, and bioinformatic analysis using two samples: a simplified, laboratory-assembled human intestinal model and a human fecal sample. We observe that variability at the peptide level is predominantly due to sample processing workflows, with a smaller contribution of bioinformatic pipelines. These peptide-level differences largely disappear at the protein group level. While differences are observed for predicted community composition, similar functional profiles are obtained across workflows. CAMPI demonstrates the robustness of present-day metaproteomics research, serves as a template for multi-laboratory studies in metaproteomics, and provides publicly available data sets for benchmarking future developments.

6 September 2019 in Frontiers in Microbiology
Verified
Journal Article
Open access
PDF file
KHKarim Hayoun
Karim Hayoun
DGDuarte Gouveia
Duarte Gouveia
LGLucia Grenga
Lucia Grenga
OPOlivier Pible
Olivier Pible
Jean ArmengaudJean Armengaud
Jean Armengaud
BABEATRICE ALPHA-BAZIN
BEATRICE ALPHA-BAZIN
Tandem mass spectrometry-based proteotyping allows characterizing microorganisms in terms of taxonomy and is becoming an important tool for investigating microbial diversity from several ecosystems. Fast and automatable sample preparation for obtaining peptide pools amenable to tandem mass spectrometry is necessary for enabling proteotyping as a high-throughput method. First, the protocol to increase the yield of lysis of several representative bacterial and eukaryotic microorganisms was optimized by using a long and drastic bead-beating setting with 0.1 mm silica beads, 0.1 and 0.5 mm glass beads, in presence of detergents. Then, three different methods to obtain greater digestion yield from these extracts were tested and optimized for improve efficiency and reduce application time: denaturing electrophoresis of proteins and in-gel proteolysis, suspension-trapping filter-based approach (S-Trap) and, solid-phase-enhanced sample preparation named SP3. The latter method outperforms the other two in terms of speed and delivers also more peptides and proteins than with the in-gel proteolysis (2.2 fold for both) and S-trap approaches (1.3 and 1.2 fold, respectively). Thus, SP3 directly improves tandem mass spectrometry proteotyping.

1 February 2007 in Biochemistry
Verified
Journal Article
Closed access
CVClaude Vidaud
Claude Vidaud
SGSamuel Gourion-Arsiquaud
Samuel Gourion-Arsiquaud
FRFrançoise Rollin-Genetet
Françoise Rollin-Genetet
CTCaroline Torne-Celer
Caroline Torne-Celer
SPSophie Plantevin
Sophie Plantevin
EQEric Quéméneur
Eric Quéméneur

1 April 2019 in Journal of Proteomics
Verified
Journal Article
Open access
DGDuarte Gouveia
Duarte Gouveia
CAChristine Almunia
Christine Almunia
YCYannick Cogne
Yannick Cogne
OPOlivier Pible
Olivier Pible
DEDavide Degli Esposti
Davide Degli Esposti
Jean ArmengaudJean Armengaud
Jean Armengaud
Anthropogenic pollutants are found worldwide. Their fate and effects on human and ecosystem health must be appropriately monitored. Today, ecotoxicology is focused on the development of new methods to assess the impact of pollutant toxicity on living organisms and ecosystems. In situ biomonitoring often uses sentinel animals for which, ideally, molecular biomarkers have been defined thanks to which environmental quality can be assessed. In this context, high-throughput proteomics methods offer an attractive approach to study the early molecular responses of organisms to environmental stressors. This approach can be used to identify toxicity pathways, to quantify more precisely novel biomarkers, and to draw the possible adverse outcome pathways. In this review, we discuss the major advances in ecotoxicoproteomics made over the last decade and present the current state of knowledge, emphasizing the technological and conceptual advancements that allowed major breakthroughs in this field, which aims to "make our planet great again". SIGNIFICANCE: Ecotoxicoproteomics is a protein-centric methodology that is useful for ecotoxicology and could have future applications as part of chemical risk assessment and environmental monitoring. Ecotoxicology employing non-model sentinel organisms with highly divergent phylogenetic backgrounds aims to preserve the functioning of ecosystems and the overall range of biological species supporting them. The classical proteomics workflow involves protein identification, functional annotation, and extrapolation of toxicity across species. Thus, it is essential to develop multi-omics approaches in order to unravel molecular information and construct the most suitable databases for protein identification and pathway analysis in non-model species. Current instrumentation and available software allow relevant combined transcriptomic/proteomic studies to be performed for almost any species. This review summarizes these approaches and illustrates how they can be implemented in ecotoxicology for routine biomonitoring.