Peter J. Peters

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Peter J. Peters (born 22 August 1957) is a professor of nanobiology and a distinguished university professor at Maastricht University. Peters is best known for his work in electron microscopy (EM) and cellular immunology. He is the founder and director of the Institute of Nanoscopy. [1]

Contents

Early life and education

Peters was born in Hunsel, the Netherlands in 1957. [2] The eldest of six children, he often accompanied his father—a farmer—on errands. On one such visit to a local artificial insemination station, Peters discovered a keen interest in science.

Peters obtained his PhD in 1991 from Utrecht University. [3] His PhD thesis, "Cellular immunology at the subcellular level", was completed under the guidance of Hans Geuze, Jannie Borst, and Hidde Ploegh. During this time, he studied the ultrastructure and trafficking of MHC class II molecules, [4] [5] [6] as well as how the role of secretory granules in T-cell function. [4] [7] Following his PhD, Peters completed a postdoctoral fellowship at the National Institutes of Health in the laboratory of Richard Klausner, where he studied the regulation of endocytosis. [4] [8]

Career

From 1994 to 1998, Peters worked at Utrecht University. He then moved on to the Netherlands Cancer Institute, where he worked from 1998 to 2013. There his group focused on sorting within the eukaryotic cell endomembrane system, primarily using cryo immunogold-electron microscopy. [4] [9] In 2014, Peters was appointed professor of nanobiology and co-director of the Maastricht Multimodal Molecular Imaging Institute at Maastricht University. [1] [2]

Since 1988, Peters has collaborated with Hans Clevers, working to establish human tissue organoids from stem cells in order to study the origin and mechanism of cancer and infection.

Peters’s current research goal is to devise a way of doing cryo-electron tomography in order to give a 3D view of a cell’s internal structure. His research group under M4I’s Division of Nanoscopy studies the 3D structure of an important component of the nanomachinery in bacteria causing tuberculosis.

Other professional activities

Peters hold patents for three inventions, with a fourth filed and pending. One of his innovations resulted in a commercial product used in EM, currently sold by Leica Microsystems.

Peters is a member of the American Society of Cell Biology and the European Society of Microscopy. In 2016, he was elected to the Netherlands Academy of Technology and Innovation. [10] He has frequently chaired international conferences and symposia, most recently the 19th International Microscopy Conference in Sydney, Australia in 2018. [11]

Peters founded the Netherlands Postdoc Career Development Initiative (PDCI) in 1998 and served as its dean until 2002. PDCI was highlighted in the international press, in Cell, [12] [13] The Scientist, [14] and Nature. [15] Peters was editor of the journal Microscopy (formerly the Journal of Electron Microscopy) from 2008 to 2012.

In 2009, Peters was invited by the Society of Histochemistry to deliver the Robert Feulgen lecture. [16]

In 2010–2011, Peters led the initiative and coordinated the establishment of the Netherlands Centre for Electron Nanoscopy, a Dutch national research infrastructure.[ citation needed ]

Publications

Peters has published over 125 papers that have been cited over 24,000 times. [17] His Hirsch index is 69.

Related Research Articles

<span class="mw-page-title-main">Endocytosis</span> Cellular process

Endocytosis is a cellular process in which substances are brought into the cell. The material to be internalized is surrounded by an area of cell membrane, which then buds off inside the cell to form a vesicle containing the ingested materials. Endocytosis includes pinocytosis and phagocytosis. It is a form of active transport.

<span class="mw-page-title-main">Structural biology</span> Study of molecular structures in biology

Structural biology, as defined by the Journal of Structural Biology, deals with structural analysis of living material at every level of organization.

An epitope, also known as antigenic determinant, is the part of an antigen that is recognized by the immune system, specifically by antibodies, B cells, or T cells. The part of an antibody that binds to the epitope is called a paratope. Although epitopes are usually non-self proteins, sequences derived from the host that can be recognized are also epitopes.

<span class="mw-page-title-main">MHC class I</span> Protein of the immune system

MHC class I molecules are one of two primary classes of major histocompatibility complex (MHC) molecules and are found on the cell surface of all nucleated cells in the bodies of vertebrates. They also occur on platelets, but not on red blood cells. Their function is to display peptide fragments of proteins from within the cell to cytotoxic T cells; this will trigger an immediate response from the immune system against a particular non-self antigen displayed with the help of an MHC class I protein. Because MHC class I molecules present peptides derived from cytosolic proteins, the pathway of MHC class I presentation is often called cytosolic or endogenous pathway.

<span class="mw-page-title-main">PIPES</span> Chemical compound

PIPES is a frequently used buffering agent in biochemistry. It is an ethanesulfonic acid buffer developed by Good et al. in the 1960s.

<span class="mw-page-title-main">STED microscopy</span> Technique in fluorescence microscopy

Stimulated emission depletion (STED) microscopy is one of the techniques that make up super-resolution microscopy. It creates super-resolution images by the selective deactivation of fluorophores, minimizing the area of illumination at the focal point, and thus enhancing the achievable resolution for a given system. It was developed by Stefan W. Hell and Jan Wichmann in 1994, and was first experimentally demonstrated by Hell and Thomas Klar in 1999. Hell was awarded the Nobel Prize in Chemistry in 2014 for its development. In 1986, V.A. Okhonin had patented the STED idea. This patent was unknown to Hell and Wichmann in 1994.

<span class="mw-page-title-main">MHC class II</span> Protein of the immune system

MHC Class II molecules are a class of major histocompatibility complex (MHC) molecules normally found only on professional antigen-presenting cells such as dendritic cells, macrophages, some endothelial cells, thymic epithelial cells, and B cells. These cells are important in initiating immune responses.

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<span class="mw-page-title-main">CD63</span> Mammalian protein found in Homo sapiens

CD63 antigen is a protein that, in humans, is encoded by the CD63 gene. CD63 is mainly associated with membranes of intracellular vesicles, although cell surface expression may be induced.

<span class="mw-page-title-main">TAP1</span> Protein-coding gene in the species Homo sapiens

Transporter associated with antigen processing 1 (TAP1) is a protein that in humans is encoded by the TAP1 gene. A member of the ATP-binding cassette transporter family, it is also known as ABCB2.

<i>CD82</i> (gene) Mammalian protein found in Homo sapiens

CD82, or KAI1, is a human protein encoded by the CD82 gene.

<span class="mw-page-title-main">Tripeptidyl peptidase II</span> Protein-coding gene in the species Homo sapiens

Tripeptidyl-peptidase 2 is an enzyme that in humans is encoded by the TPP2 gene. Among other things it is heavily implicated in MHC (HLA) class-I processing, as it has both endopeptidase and exopeptidase activity.

Super-resolution microscopy is a series of techniques in optical microscopy that allow such images to have resolutions higher than those imposed by the diffraction limit, which is due to the diffraction of light. Super-resolution imaging techniques rely on the near-field or on the far-field. Among techniques that rely on the latter are those that improve the resolution only modestly beyond the diffraction-limit, such as confocal microscopy with closed pinhole or aided by computational methods such as deconvolution or detector-based pixel reassignment, the 4Pi microscope, and structured-illumination microscopy technologies such as SIM and SMI.

<span class="mw-page-title-main">Immunogold labelling</span> Staining technique used in electron microscopy

Immunogold labeling or immunogold staining (IGS) is a staining technique used in electron microscopy. This staining technique is an equivalent of the indirect immunofluorescence technique for visible light. Colloidal gold particles are most often attached to secondary antibodies which are in turn attached to primary antibodies designed to bind a specific antigen or other cell component. Gold is used for its high electron density which increases electron scatter to give high contrast 'dark spots'.

Immunoevasins are proteins expressed by some viruses that enable the virus to evade immune recognition by interfering with MHC I complexes in the infected cell, therefore blocking the recognition of viral protein fragments by CD8+ cytotoxic T lymphocytes. Less frequently, MHC II antigen presentation and induced-self molecules may also be targeted. Some viral immunoevasins block peptide entry into the endoplasmic reticulum (ER) by targeting the TAP transporters. Immunoevasins are particularly abundant in viruses that are capable of establishing long-term infections of the host, such as herpesviruses.

<span class="mw-page-title-main">Jean Pieters</span> Dutch biochemist

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<span class="mw-page-title-main">Hidde Ploegh</span>

Hidde Lolke Ploegh is an immunologist at Boston Children's Hospital, known for his contributions in understanding antigen processing and the evasion of the immune system by viruses.

<span class="mw-page-title-main">Jacques Neefjes</span> Dutch biochemist

Jacques (Sjaak) Neefjes is a Dutch scientist who made breakthroughs in several research disciplines such as immunology, cell biology, chemistry, cancer biology, microbiology, and epidemiology. He is a professor at the Leiden University Medical Center. In 2020 he was one of four winners of the Spinoza Prize.

<span class="mw-page-title-main">Ron Heeren</span> Dutch mass spectrometry researcher

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<span class="mw-page-title-main">Deborah F. Kelly</span> American biomedical engineer

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References

  1. 1 2 "Distinguished university professors". Maastricht University. Retrieved 7 November 2021.
  2. 1 2 "Top nanobiologist Peter Peters to Maastricht University". Instruct Integrating Biology. Retrieved 16 August 2018.
  3. "Prof. Peter J. Peters from Maastricht University of the Netherlands made a BEI Shinzhang Lecutre". Chinese Academy of Sciences. July 2016. Retrieved 16 August 2018.
  4. 1 2 3 4 "Peter Peters Group". Netherlands Cancer Institute. Retrieved 16 August 2018.
  5. Peters, Peter J.; Neefjes, Jacques J.; Oorschot, Viola; Ploegh, Hidde L.; Geuze, Hans J. (1991). "Segregation of MHC class II molecules from MHC class I molecules in the Golgi complex for transport to lysosomal compartments". Nature. 349 (6311): 669–676. doi:10.1038/349669a0. ISSN   1476-4687. PMID   1847504. S2CID   4242062.
  6. Peters, P. J.; Raposo, G.; Neefjes, J. J.; Oorschot, V.; Leijendekker, R. L.; Geuze, H. J.; Ploegh, H. L. (1995-08-01). "Major histocompatibility complex class II compartments in human B lymphoblastoid cells are distinct from early endosomes". Journal of Experimental Medicine. 182 (2): 325–334. doi:10.1084/jem.182.2.325. ISSN   0022-1007. PMC   2192145 . PMID   7629497.
  7. Peters, P. J.; Borst, J.; Oorschot, V.; Fukuda, M.; Krähenbühl, O.; Tschopp, J.; Slot, J. W.; Geuze, H. J. (1991-05-01). "Cytotoxic T lymphocyte granules are secretory lysosomes, containing both perforin and granzymes". Journal of Experimental Medicine. 173 (5): 1099–1109. doi:10.1084/jem.173.5.1099. ISSN   0022-1007. PMC   2118839 . PMID   2022921.
  8. Peters, P. J.; Hsu, V. W.; Ooi, C. E.; Finazzi, D.; Teal, S. B.; Oorschot, V.; Donaldson, J. G.; Klausner, R. D. (1995-03-15). "Overexpression of wild-type and mutant ARF1 and ARF6: distinct perturbations of nonoverlapping membrane compartments". J Cell Biol. 128 (6): 1003–1017. doi:10.1083/jcb.128.6.1003. ISSN   0021-9525. PMC   2120412 . PMID   7896867.
  9. van der Wel, Nicole; Hava, David; Houben, Diane; Fluitsma, Donna; Zon, Maaike van; Pierson, Jason; Brenner, Michael; Peters, Peter J. (2007). "M. tuberculosis and M. leprae Translocate from the Phagolysosome to the Cytosol in Myeloid Cells". Cell. 129 (7): 1287–1298. doi: 10.1016/j.cell.2007.05.059 . PMID   17604718.
  10. "Bestuur en leden – AcTI".
  11. "19th International Microscopy Congress (IMC19)".
  12. Aschwanden, Christie (2006). "Professionalizing the Postdoctoral Experience". Cell. 124 (3): 445–447. doi: 10.1016/j.cell.2006.01.025 . PMID   16469686.
  13. Aschwanden, Christie (2006). "Learning to Lead". Cell. 125 (3): 407–409. doi: 10.1016/j.cell.2006.04.017 . PMID   16678082.
  14. "Best Places to Work 2008: Postdocs". The Scientist. Retrieved 2018-01-23.
  15. Griekspoor, Alexander (2007-02-21). "Torn between two ladders". Nature. 445 (7130): 948. doi: 10.1038/nj7130-948b .
  16. "Robert Feulgen Lectures". Society for Histochemistry. Retrieved 16 August 2018.
  17. "PJ Peters citations".