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A subcellular map of the human proteome
KTH, Skolan för bioteknologi (BIO), Proteomik och nanobioteknologi. KTH, Centra, Science for Life Laboratory, SciLifeLab.ORCID-id: 0000-0002-6107-1465
KTH, Skolan för bioteknologi (BIO). KTH, Centra, Science for Life Laboratory, SciLifeLab.
KTH, Skolan för bioteknologi (BIO), Proteomik och nanobioteknologi. KTH, Centra, Science for Life Laboratory, SciLifeLab.ORCID-id: 0000-0002-6368-6690
KTH, Skolan för bioteknologi (BIO), Proteomik och nanobioteknologi. KTH, Centra, Science for Life Laboratory, SciLifeLab.
Visa övriga samt affilieringar
2017 (Engelska)Ingår i: Science, ISSN 0036-8075, E-ISSN 1095-9203, Vol. 356, nr 6340, artikel-id 820Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Resolving the spatial distribution of the human proteome at a subcellular level can greatly increase our understanding of human biology and disease. Here we present a comprehensive image-based map of subcellular protein distribution, the Cell Atlas, built by integrating transcriptomics and antibody-based immunofluorescence microscopy with validation by mass spectrometry. Mapping the in situ localization of 12,003 human proteins at a single-cell level to 30 subcellular structures enabled the definition of the proteomes of 13 major organelles. Exploration of the proteomes revealed single-cell variations in abundance or spatial distribution and localization of about half of the proteins to multiple compartments. This subcellular map can be used to refine existing protein-protein interaction networks and provides an important resource to deconvolute the highly complex architecture of the human cell.

Ort, förlag, år, upplaga, sidor
American Association for the Advancement of Science , 2017. Vol. 356, nr 6340, artikel-id 820
Nyckelord [en]
antibody, proteome, biology, cells and cell components, disease incidence, image analysis, physiological response, protein, proteomics, spatial distribution, Article, cell organelle, cellular distribution, human, human cell, immunofluorescence microscopy, mass spectrometry, priority journal, protein analysis, protein localization, protein protein interaction, single cell analysis, transcriptomics
Nationell ämneskategori
Cellbiologi
Identifikatorer
URN: urn:nbn:se:kth:diva-216588DOI: 10.1126/science.aal3321ISI: 000401957900032Scopus ID: 2-s2.0-85019201137OAI: oai:DiVA.org:kth-216588DiVA, id: diva2:1164056
Anmärkning

QC 20171208

Tillgänglig från: 2017-12-08 Skapad: 2017-12-08 Senast uppdaterad: 2019-10-03Bibliografiskt granskad
Ingår i avhandling
1. Spatiotemporal characterization of the human proteome
Öppna denna publikation i ny flik eller fönster >>Spatiotemporal characterization of the human proteome
2019 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Characterizing the molecular components of the basic unit of life; the cell, is crucial for a complete understanding of human biology. The cell is divided into compartments to create a suitable environment for the resident proteins to fulfill their functions. Therefore, spatial mapping of the human proteome is essential to understand protein function in health and disease.

 

Spatial proteomics is most commonly investigated using mass spectrometry or imaging, combined with machine learning for the data analysis. Until now, studies have been limited to high abundant proteins and relied on the purification of organelle fractions from a bulk of cells. Within the scope of this thesis, we were able to systematically localize proteins in their native cellular environment using antibody-based imaging techniques, and to investigate protein subcellular localization and dynamics on a single cell level, introducing a major advance within the field of spatial proteomics.

 

Paper I of this thesis presents a subcellular map of the human proteome, where the spatial distribution of 12,003 human proteins was mapped into 30 subcellular structures, half of which were not previously localized. Besides providing a valuable dataset for cell biology, this study is the first to reveal the spatial complexity of human cells with proteins localizing to multiple compartments and pronounced single cell variations. Paper II reports on the systematic temporal dissection of these single cell variations and the identification of cell cycle correlated variations. We identified 258 novel cell cycle regulated proteins and showed that several of these proteins may be connected to proliferative diseases. A key finding of Paper II is that proteins showing non-cell cycle dependent variations are significantly enriched in mitochondria, whereas cell cycle dependent proteins are enriched in nucleoli. In Paper III and IV, we spatiotemporally characterized the proteomes of these two organelles, mitochondria and nucleoli, in greater detail.

In Paper III, we expanded the mitochondrial proteome with 560 novel proteins. As many as 20% of the mitochondrial proteome showed variations in their expression pattern at the single cell level, most often independent of the cell cycle. Paper IV provides a complete characterization of the nucleolar proteome. Nucleoli are not only important for ribosome synthesis and assembly, but are also crucial for cell cycle regulation through the recruitment of its proteins to the chromosomal periphery during cell division. Here, we presented the first proteome-wide spatiotemporal analysis of the nucleolus with its sub-compartments, and identified 69 nucleolar proteins that relocated to the chromosomes periphery during mitosis.

 

In conclusion, this thesis unravels the spatiotemporal proteome organization of the human cell over the course of a cell cycle and offers a valuable starting point for a better understanding of human cell biology in health and disease.

Ort, förlag, år, upplaga, sidor
Stockholm, Sweden: KTH Royal Institute of Technology, 2019. s. 65
Serie
TRITA-CBH-FOU ; 2019:48
Nyckelord
Spatial proteomics, Spatiotemporal proteomics, Immunofluorescence, Human Protein Atlas, Cell compartments, Single cell proteomics, Cell cycle, Cancer
Nationell ämneskategori
Cell- och molekylärbiologi Biologiska vetenskaper
Identifikatorer
urn:nbn:se:kth:diva-261245 (URN)978-91-7873-302-6 (ISBN)
Disputation
2019-10-25, Atrium, Nobels väg 12B, Wargentinhuset, solna, 09:00 (Engelska)
Opponent
Handledare
Forskningsfinansiär
Science for Life Laboratory - a national resource center for high-throughput molecular bioscience
Anmärkning

QC 2019-10-04

Tillgänglig från: 2019-10-04 Skapad: 2019-10-03 Senast uppdaterad: 2019-10-04Bibliografiskt granskad

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Av författaren/redaktören
Thul, Peter J.Åkesson, LovisaWiking, MikaelaMahdessian, DianaAit Blal, HammouAlm, Tove L.Björk, LarsBäckström, AnnaDanielsson, FridaFagerberg, LinnFall, JennyGnann, ChristianHober, SophiaHjelmare, MartinJohansson, FredricLee, SunjaeNilsson, PeterOksvold, PerRockberg, JohanSchutten, RutgerSchwenk, Jochen M.Sivertsson, ÅsaSkogs, MarieStadler, CharlotteSullivan, Devin P.Tegel, HannaWinsnes, Casper F.Zhang, ChengZwahlen, MartinMardinoglu, Adilvon Feilitzen, KalleUhlén, MathiasLundberg, Emma
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Proteomik och nanobioteknologiScience for Life Laboratory, SciLifeLabSkolan för bioteknologi (BIO)Proteinteknologi
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