Protein misfolding cyclic amplification of infectious prions
Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory has been a major limitation to the study of the unorthodox nature of this infectious agent and the molecular mechanism by which the normal p...
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Published in | Nature protocols Vol. 7; no. 7; pp. 1397 - 1409 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
28.06.2012
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1754-2189 1750-2799 1750-2799 |
DOI | 10.1038/nprot.2012.067 |
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Abstract | Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory has been a major limitation to the study of the unorthodox nature of this infectious agent and the molecular mechanism by which the normal prion protein (PrP
C
) is converted into the abnormal isoform (PrP
Sc
). Protein misfolding cyclic amplification (PMCA), described in detail in this protocol, is a simple, fast and efficient methodology to mimic prion replication in the test tube. PMCA involves incubating materials containing minute amounts of infectious prions with an excess of PrP
C
and boosting the conversion by cycles of sonication to fragment the converting units, thereby leading to accelerated prion replication. PMCA is able to detect the equivalent of a single molecule of infectious PrP
Sc
and propagate prions that maintain high infectivity, strain properties and species specificity. A single PMCA assay takes little more than 3 d to replicate a large amount of prions, which could take years in an
in vivo
situation. Since its invention 10 years ago, PMCA has helped to answer fundamental questions about this intriguing infectious agent and has been broadly applied in research areas that include the food industry, blood bank safety and human and veterinary disease diagnosis. |
---|---|
AbstractList | Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory has been a major limitation to the study of the unorthodox nature of this infectious agent and the molecular mechanism by which the normal prion protein (PrP(C)) is converted into the abnormal isoform (PrP(Sc)). Protein misfolding cyclic amplification (PMCA), described in detail in this protocol, is a simple, fast and efficient methodology to mimic prion replication in the test tube. PMCA involves incubating materials containing minute amounts of infectious prions with an excess of PrP(C) and boosting the conversion by cycles of sonication to fragment the converting units, thereby leading to accelerated prion replication. PMCA is able to detect the equivalent of a single molecule of infectious PrP(Sc) and propagate prions that maintain high infectivity, strain properties and species specificity. A single PMCA assay takes little more than 3 d to replicate a large amount of prions, which could take years in an in vivo situation. Since its invention 10 years ago, PMCA has helped to answer fundamental questions about this intriguing infectious agent and has been broadly applied in research areas that include the food industry, blood bank safety and human and veterinary disease diagnosis. Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory has been a major limitation to the study of the unorthodox nature of this infectious agent and the molecular mechanism by which the normal prion protein (PrP C ) is converted into the abnormal isoform (PrP Sc ). Protein misfolding cyclic amplification (PMCA), described in detail in this protocol, is a simple, fast and efficient methodology to mimic prion replication in the test tube. PMCA involves incubating materials containing minute amounts of infectious prions with an excess of PrP C and boosting the conversion by cycles of sonication to fragment the converting units, thereby leading to accelerated prion replication. PMCA is able to detect the equivalent of a single molecule of infectious PrP Sc and propagate prions that maintain high infectivity, strain properties and species specificity. A single PMCA assay takes little more than 3 d to replicate a large amount of prions, which could take years in an in vivo situation. Since its invention 10 years ago, PMCA has helped to answer fundamental questions about this intriguing infectious agent and has been broadly applied in research areas that include the food industry, blood bank safety and human and veterinary disease diagnosis. Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory has been a major limitation to the study of the unorthodox nature of this infectious agent and the molecular mechanism by which the normal prion protein (PrPC) is converted into the abnormal isoform (PrPSc). Protein misfolding cyclic amplification (PMCA), described in detail in this protocol, is a simple, fast and efficient methodology to mimic prion replication in the test tube. PMCA involves incubating materials containing minute amounts of infectious prions with an excess of PrPC and boosting the conversion by cycles of sonication to fragment the converting units, thereby leading to accelerated prion replication. PMCA is able to detect the equivalent of a single molecule of infectious PrPSc and propagate prions that maintain high infectivity, strain properties and species specificity. A single PMCA assay takes little more than 3 d to replicate a large amount of prions, which could take years in an in vivo situation. Since its invention 10 years ago, PMCA has helped to answer fundamental questions about this intriguing infectious agent and has been broadly applied in research areas that include the food industry, blood bank safety and human and veterinary disease diagnosis. Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory has been a major limitation to the study of the unorthodox nature of this infectious agent and the molecular mechanism by which the normal prion protein (PrP(C)) is converted into the abnormal isoform (PrP(Sc)). Protein misfolding cyclic amplification (PMCA), described in detail in this protocol, is a simple, fast and efficient methodology to mimic prion replication in the test tube. PMCA involves incubating materials containing minute amounts of infectious prions with an excess of PrP(C) and boosting the conversion by cycles of sonication to fragment the converting units, thereby leading to accelerated prion replication. PMCA is able to detect the equivalent of a single molecule of infectious PrP(Sc) and propagate prions that maintain high infectivity, strain properties and species specificity. A single PMCA assay takes little more than 3 d to replicate a large amount of prions, which could take years in an in vivo situation. Since its invention 10 years ago, PMCA has helped to answer fundamental questions about this intriguing infectious agent and has been broadly applied in research areas that include the food industry, blood bank safety and human and veterinary disease diagnosis.Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory has been a major limitation to the study of the unorthodox nature of this infectious agent and the molecular mechanism by which the normal prion protein (PrP(C)) is converted into the abnormal isoform (PrP(Sc)). Protein misfolding cyclic amplification (PMCA), described in detail in this protocol, is a simple, fast and efficient methodology to mimic prion replication in the test tube. PMCA involves incubating materials containing minute amounts of infectious prions with an excess of PrP(C) and boosting the conversion by cycles of sonication to fragment the converting units, thereby leading to accelerated prion replication. PMCA is able to detect the equivalent of a single molecule of infectious PrP(Sc) and propagate prions that maintain high infectivity, strain properties and species specificity. A single PMCA assay takes little more than 3 d to replicate a large amount of prions, which could take years in an in vivo situation. Since its invention 10 years ago, PMCA has helped to answer fundamental questions about this intriguing infectious agent and has been broadly applied in research areas that include the food industry, blood bank safety and human and veterinary disease diagnosis. |
Author | Duran-Aniotz, Claudia Diaz-Espinoza, Rodrigo Soto, Claudio Camacho, Manuel V Morales, Rodrigo |
AuthorAffiliation | 1 Mitchell Center for Alzheimer’s Disease and Related Brain Disorders, Department of Neurology, University of Texas Houston Medical School, Houston, Texas, USA 2 Facultad de Medicina, Universidad de los Andes, Santiago, Chile |
AuthorAffiliation_xml | – name: 1 Mitchell Center for Alzheimer’s Disease and Related Brain Disorders, Department of Neurology, University of Texas Houston Medical School, Houston, Texas, USA – name: 2 Facultad de Medicina, Universidad de los Andes, Santiago, Chile |
Author_xml | – sequence: 1 givenname: Rodrigo surname: Morales fullname: Morales, Rodrigo organization: Department of Neurology, Mitchell Center for Alzheimer's Disease and Related Brain Disorders, University of Texas Houston Medical School – sequence: 2 givenname: Claudia surname: Duran-Aniotz fullname: Duran-Aniotz, Claudia organization: Department of Neurology, Mitchell Center for Alzheimer's Disease and Related Brain Disorders, University of Texas Houston Medical School, Facultad de Medicina, Universidad de los Andes – sequence: 3 givenname: Rodrigo surname: Diaz-Espinoza fullname: Diaz-Espinoza, Rodrigo organization: Department of Neurology, Mitchell Center for Alzheimer's Disease and Related Brain Disorders, University of Texas Houston Medical School – sequence: 4 givenname: Manuel V surname: Camacho fullname: Camacho, Manuel V organization: Department of Neurology, Mitchell Center for Alzheimer's Disease and Related Brain Disorders, University of Texas Houston Medical School – sequence: 5 givenname: Claudio surname: Soto fullname: Soto, Claudio email: claudio.soto@uth.tmc.edu organization: Department of Neurology, Mitchell Center for Alzheimer's Disease and Related Brain Disorders, University of Texas Houston Medical School |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22743831$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/S0140-6736(04)15486-X 10.1038/nrmicro1003 10.1073/pnas.0702662104 10.1038/35081095 10.1128/jvi.66.4.2096-2101.1992 10.1016/S0140-6736(06)69835-8 10.1038/nmeth.1465 10.1111/j.1750-3639.1996.tb00796.x 10.1371/journal.pone.0007990 10.1016/1074-5521(95)90087-X 10.1371/journal.ppat.1000139 10.1128/JVI.00635-07 10.1074/jbc.M603964200 10.1016/0092-8674(93)90635-4 10.1146/annurev.neuro.24.1.519 10.1016/j.virol.2008.09.023 10.1016/S0140-6736(96)08496-6 10.1126/science.1183748 10.1016/S0166-2236(02)02195-1 10.1074/jbc.M110.198465 10.1016/j.febslet.2010.04.040 10.1126/science.1129051 10.1016/S0140-6736(96)01310-4 10.1016/j.febslet.2008.08.003 10.1371/journal.pone.0020384 10.1038/emboj.2008.181 10.1038/nm1286 10.1016/j.neulet.2006.11.056 10.1099/vir.0.82786-0 10.1126/science.1187790 10.1016/j.tibs.2006.01.002 10.1016/j.cell.2005.02.011 10.1073/pnas.95.23.13363 10.1371/journal.ppat.1000421 10.1021/bi100370b 10.1371/journal.pone.0004848 10.1016/j.cell.2008.07.030 10.1371/journal.ppat.1002370 10.1016/S0140-6736(04)16811-6 10.1016/j.tibs.2010.11.001 10.1111/j.1537-2995.2010.02595.x 10.4161/pri.3.3.9819 10.1371/journal.ppat.1001277 10.1016/j.bbrc.2010.06.013 10.1128/JVI.77.15.8462-8469.2003 10.1016/j.bbrc.2008.09.141 10.1099/vir.0.2008/004226-0 |
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References | Soto (CR8) 2011; 36 Jarrett, Lansbury (CR14) 1993; 73 Murayama (CR34) 2007; 88 Castilla (CR21) 2008; 27 Barret (CR38) 2003; 77 Soto, Satani (CR9) 2011; 36 Haley, Seelig, Zabel, Telling, Hoover (CR40) 2009; 4 Supattapone (CR27) 2010; 327 Collinge (CR2) 2001; 24 Soto, Estrada, Castilla (CR15) 2006; 31 Saborio, Permanne, Soto (CR10) 2001; 411 Nagaoka (CR43) 2010; 397 Kurt (CR47) 2007; 81 Wroe (CR7) 2006; 368 Soto (CR31) 2004; 2 Morales (CR39) 2008; 377 Collee, Bradley (CR4) 1997; 349 Peden, Head, Ritchie, Bell, Ironside (CR6) 2004; 364 Abid, Morales, Soto (CR26) 2010; 584 Fernandez-Borges, Castilla (CR19) 2010; 4 Deleault, Kascsak, Geoghegan, Supattapone (CR28) 2010; 49 Tattum, Jones, Pal, Collinge, Jackson (CR35) 2010; 50 Saa, Castilla, Soto (CR17) 2006; 281 Green (CR22) 2008; 4 Barria, Telling, Gambetti, Mastrianni, Soto (CR46) 2011; 286 Collee, Bradley (CR3) 1997; 349 Caughey, Kocisko, Raymond, Lansbury (CR12) 1995; 2 Castilla, Saá, Hetz, Soto (CR16) 2005; 121 Castilla (CR29) 2008; 134 Soto, Saborio, Anderes (CR11) 2002; 25 Chen, Morales, Barria, Soto (CR37) 2010; 7 Ghetti (CR13) 1996; 6 Llewelyn (CR5) 2004; 363 Gonzalez-Montalban (CR18) 2011; 7 Murayama (CR45) 2006; 413 Saa, Castilla, Soto (CR36) 2006; 313 Prusiner (CR1) 1998; 95 Gonzalez-Romero, Barria, Leon, Morales, Soto (CR33) 2008; 582 Thorne, Terry (CR49) 2008; 89 Wang, Wang, Yuan, Ma (CR25) 2010; 327 Nichols (CR42) 2009; 3 Cosseddu (CR48) 2011; 7 Deleault, Harris, Rees, Supattapone (CR24) 2007; 104 Castilla, Saa, Soto (CR32) 2005; 11 Bessen, Marsh (CR44) 1992; 66 Barria, Mukherjee, Gonzalez-Romero, Morales, Soto (CR30) 2009; 5 Meyerett (CR23) 2008; 382 Haley, Mathiason, Zabel, Telling, Hoover (CR41) 2009; 4 Pritzkow (CR20) 2011; 6 JG Collee (BFnprot2012067_CR3) 1997; 349 NR Deleault (BFnprot2012067_CR28) 2010; 49 C Soto (BFnprot2012067_CR31) 2004; 2 J Castilla (BFnprot2012067_CR16) 2005; 121 SJ Wroe (BFnprot2012067_CR7) 2006; 368 B Ghetti (BFnprot2012067_CR13) 1996; 6 C Soto (BFnprot2012067_CR11) 2002; 25 J Castilla (BFnprot2012067_CR32) 2005; 11 MH Tattum (BFnprot2012067_CR35) 2010; 50 MA Barria (BFnprot2012067_CR46) 2011; 286 C Soto (BFnprot2012067_CR9) 2011; 36 NJ Haley (BFnprot2012067_CR40) 2009; 4 A Barret (BFnprot2012067_CR38) 2003; 77 NR Deleault (BFnprot2012067_CR24) 2007; 104 P Saa (BFnprot2012067_CR17) 2006; 281 Y Murayama (BFnprot2012067_CR34) 2007; 88 S Pritzkow (BFnprot2012067_CR20) 2011; 6 S Supattapone (BFnprot2012067_CR27) 2010; 327 TD Kurt (BFnprot2012067_CR47) 2007; 81 Y Murayama (BFnprot2012067_CR45) 2006; 413 JT Jarrett (BFnprot2012067_CR14) 1993; 73 F Wang (BFnprot2012067_CR25) 2010; 327 J Castilla (BFnprot2012067_CR21) 2008; 27 JG Collee (BFnprot2012067_CR4) 1997; 349 B Caughey (BFnprot2012067_CR12) 1995; 2 J Castilla (BFnprot2012067_CR29) 2008; 134 NJ Haley (BFnprot2012067_CR41) 2009; 4 L Thorne (BFnprot2012067_CR49) 2008; 89 MA Barria (BFnprot2012067_CR30) 2009; 5 N Gonzalez-Montalban (BFnprot2012067_CR18) 2011; 7 R Morales (BFnprot2012067_CR39) 2008; 377 TA Nichols (BFnprot2012067_CR42) 2009; 3 SB Prusiner (BFnprot2012067_CR1) 1998; 95 B Chen (BFnprot2012067_CR37) 2010; 7 GM Cosseddu (BFnprot2012067_CR48) 2011; 7 C Meyerett (BFnprot2012067_CR23) 2008; 382 K Abid (BFnprot2012067_CR26) 2010; 584 GP Saborio (BFnprot2012067_CR10) 2001; 411 N Fernandez-Borges (BFnprot2012067_CR19) 2010; 4 C Soto (BFnprot2012067_CR15) 2006; 31 D Gonzalez-Romero (BFnprot2012067_CR33) 2008; 582 CA Llewelyn (BFnprot2012067_CR5) 2004; 363 K Nagaoka (BFnprot2012067_CR43) 2010; 397 J Collinge (BFnprot2012067_CR2) 2001; 24 C Soto (BFnprot2012067_CR8) 2011; 36 KM Green (BFnprot2012067_CR22) 2008; 4 RA Bessen (BFnprot2012067_CR44) 1992; 66 AH Peden (BFnprot2012067_CR6) 2004; 364 P Saa (BFnprot2012067_CR36) 2006; 313 17553879 - J Virol. 2007 Sep;81(17):9605-8 18775309 - Cell. 2008 Sep 5;134(5):757-68 18952250 - Virology. 2008 Dec 20;382(2):267-76 1347795 - J Virol. 1992 Apr;66(4):2096-101 18706416 - FEBS Lett. 2008 Sep 22;582(21-22):3161-6 20185716 - Science. 2010 Feb 26;327(5969):1091-2 21209079 - J Biol Chem. 2011 Mar 4;286(9):7490-5 20377181 - Biochemistry. 2010 May 11;49(18):3928-34 8807814 - Chem Biol. 1995 Dec;2(12):807-17 19293928 - PLoS One. 2009;4(3):e4848 8737929 - Brain Pathol. 1996 Apr;6(2):127-45 17161728 - Lancet. 2006 Dec 9;368(9552):2061-7 20889378 - Trends Mol Med. 2011 Jan;17(1):14-24 18769716 - PLoS Pathog. 2008;4(8):e1000139 17174030 - Neurosci Lett. 2007 Feb 21;413(3):270-3 20570651 - Biochem Biophys Res Commun. 2010 Jul 2;397(3):626-30 11283320 - Annu Rev Neurosci. 2001;24:519-50 8513491 - Cell. 1993 Jun 18;73(6):1055-8 9057745 - Lancet. 1997 Mar 1;349(9052):636-41 17872544 - J Gen Virol. 2007 Oct;88(Pt 10):2890-8 21130657 - Trends Biochem Sci. 2011 Mar;36(3):151-8 18851948 - Biochem Biophys Res Commun. 2008 Dec 12;377(2):373-8 15302196 - Lancet. 2004 Aug 7-13;364(9433):527-9 21347353 - PLoS Pathog. 2011;7(2):e1001277 20512142 - Nat Methods. 2010 Jul;7(7):519-20 14962520 - Lancet. 2004 Feb 7;363(9407):417-21 19823039 - Prion. 2009 Jul-Sep;3(3):171-83 20180925 - Transfusion. 2010 May;50(5):996-1002 16127436 - Nat Med. 2005 Sep;11(9):982-5 15378045 - Nat Rev Microbiol. 2004 Oct;2(10):809-19 20110469 - Science. 2010 Feb 26;327(5969):1132-5 16473510 - Trends Biochem Sci. 2006 Mar;31(3):150-5 22114554 - PLoS Pathog. 2011 Nov;7(11):e1002370 11459061 - Nature. 2001 Jun 14;411(6839):810-3 17535913 - Proc Natl Acad Sci U S A. 2007 Jun 5;104(23):9741-6 18800058 - EMBO J. 2008 Oct 8;27(19):2557-66 19436715 - PLoS Pathog. 2009 May;5(5):e1000421 19008409 - J Gen Virol. 2008 Dec;89(Pt 12):3177-84 9811807 - Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13363-83 19956732 - PLoS One. 2009;4(11):e7990 12857915 - J Virol. 2003 Aug;77(15):8462-9 20412808 - FEBS Lett. 2010 Jun 3;584(11):2409-14 21647368 - PLoS One. 2011;6(5):e20384 16825570 - Science. 2006 Jul 7;313(5783):92-4 15851027 - Cell. 2005 Apr 22;121(2):195-206 16982620 - J Biol Chem. 2006 Nov 17;281(46):35245-52 12127750 - Trends Neurosci. 2002 Aug;25(8):390-4 9078212 - Lancet. 1997 Mar 8;349(9053):715-21 |
References_xml | – volume: 363 start-page: 417 year: 2004 end-page: 421 ident: CR5 article-title: Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion publication-title: Lancet doi: 10.1016/S0140-6736(04)15486-X – volume: 2 start-page: 809 year: 2004 end-page: 819 ident: CR31 article-title: Diagnosing prion diseases: needs, challenges and hopes publication-title: Nat. Rev. Microbiol. doi: 10.1038/nrmicro1003 – volume: 104 start-page: 9741 year: 2007 end-page: 9746 ident: CR24 article-title: Formation of native prions from minimal components publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.0702662104 – volume: 411 start-page: 810 year: 2001 end-page: 813 ident: CR10 article-title: Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding publication-title: Nature doi: 10.1038/35081095 – volume: 66 start-page: 2096 year: 1992 end-page: 2101 ident: CR44 article-title: Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent publication-title: J. Virol. doi: 10.1128/jvi.66.4.2096-2101.1992 – volume: 368 start-page: 2061 year: 2006 end-page: 2067 ident: CR7 article-title: Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report publication-title: Lancet doi: 10.1016/S0140-6736(06)69835-8 – volume: 4 start-page: 200 year: 2010 end-page: 207 ident: CR19 article-title: PMCA. A decade of prion replication publication-title: Curr. Chem. Biol. – volume: 7 start-page: 519 year: 2010 end-page: 520 ident: CR37 article-title: Estimating prion concentration in fluids and tissues by quantitative PMCA publication-title: Nat. Methods doi: 10.1038/nmeth.1465 – volume: 6 start-page: 127 year: 1996 end-page: 145 ident: CR13 article-title: Prion protein amyloidosis publication-title: Brain Pathol. doi: 10.1111/j.1750-3639.1996.tb00796.x – volume: 4 start-page: e7990 year: 2009 ident: CR41 article-title: Detection of sub-clinical CWD infection in conventional test-negative deer long after oral exposure to urine and feces from CWD deer publication-title: PLoS ONE doi: 10.1371/journal.pone.0007990 – volume: 36 start-page: 151 year: 2011 end-page: 158 ident: CR9 article-title: The intricate mechanisms of neurodegeneration in prion diseases publication-title: Trends Mol. Med. – volume: 2 start-page: 807 year: 1995 end-page: 817 ident: CR12 article-title: Aggregates of scrapie-associated prion protein induce the cell-free conversion of protease-sensitive prion protein to the protease-resistant state publication-title: Chem. Biol. doi: 10.1016/1074-5521(95)90087-X – volume: 4 start-page: e1000139 year: 2008 ident: CR22 article-title: Accelerated high fidelity prion amplification within and across prion species barriers publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1000139 – volume: 81 start-page: 9605 year: 2007 end-page: 9608 ident: CR47 article-title: Efficient amplification of chronic wasting disease PrPRES publication-title: J. Virol. doi: 10.1128/JVI.00635-07 – volume: 281 start-page: 35245 year: 2006 end-page: 35252 ident: CR17 article-title: Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification publication-title: J. Biol. Chem. doi: 10.1074/jbc.M603964200 – volume: 73 start-page: 1055 year: 1993 end-page: 1058 ident: CR14 article-title: Seeding 'one-dimensional crystallization' of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie? publication-title: Cell doi: 10.1016/0092-8674(93)90635-4 – volume: 24 start-page: 519 year: 2001 end-page: 550 ident: CR2 article-title: Prion diseases of humans and animals: their causes and molecular basis publication-title: Annu. Rev. Neurosci. doi: 10.1146/annurev.neuro.24.1.519 – volume: 382 start-page: 267 year: 2008 end-page: 276 ident: CR23 article-title: strain adaptation of CWD prions by serial protein misfolding cyclic amplification publication-title: Virology doi: 10.1016/j.virol.2008.09.023 – volume: 349 start-page: 715 year: 1997 end-page: 721 ident: CR4 article-title: BSE: a decade on—Part 2 publication-title: Lancet doi: 10.1016/S0140-6736(96)08496-6 – volume: 327 start-page: 1132 year: 2010 end-page: 1135 ident: CR25 article-title: Generating a prion with bacterially expressed recombinant prion protein publication-title: Science doi: 10.1126/science.1183748 – volume: 25 start-page: 390 year: 2002 end-page: 394 ident: CR11 article-title: Cyclic amplification of protein misfolding: application to prion-related disorders and beyond publication-title: Trends Neurosci. doi: 10.1016/S0166-2236(02)02195-1 – volume: 286 start-page: 7490 year: 2011 end-page: 7495 ident: CR46 article-title: Generation of a new form of human PrPSc by interspecies transmission from cervid prions publication-title: J. Biol. Chem. doi: 10.1074/jbc.M110.198465 – volume: 584 start-page: 2409 year: 2010 end-page: 2414 ident: CR26 article-title: Cellular factors implicated in prion replication publication-title: FEBS Lett. doi: 10.1016/j.febslet.2010.04.040 – volume: 313 start-page: 92 year: 2006 end-page: 94 ident: CR36 article-title: Presymptomatic detection of prions in blood publication-title: Science doi: 10.1126/science.1129051 – volume: 349 start-page: 636 year: 1997 end-page: 641 ident: CR3 article-title: BSE: a decade on—Part I publication-title: Lancet doi: 10.1016/S0140-6736(96)01310-4 – volume: 582 start-page: 3161 year: 2008 end-page: 3166 ident: CR33 article-title: Detection of infectious prions in urine publication-title: FEBS Lett. doi: 10.1016/j.febslet.2008.08.003 – volume: 6 start-page: e20384 year: 2011 ident: CR20 article-title: Quantitative detection and biological propagation of scrapie seeding activity facilitate use of prions as model pathogens for disinfection publication-title: PLoS ONE doi: 10.1371/journal.pone.0020384 – volume: 27 start-page: 2557 year: 2008 end-page: 2566 ident: CR21 article-title: Cell-free propagation of prion strains publication-title: EMBO J. doi: 10.1038/emboj.2008.181 – volume: 11 start-page: 982 year: 2005 end-page: 985 ident: CR32 article-title: Detection of prions in blood publication-title: Nat. Med. doi: 10.1038/nm1286 – volume: 413 start-page: 270 year: 2006 end-page: 273 ident: CR45 article-title: Efficient amplification of a mouse-adapted scrapie prion protein publication-title: Neurosci. Lett. doi: 10.1016/j.neulet.2006.11.056 – volume: 88 start-page: 2890 year: 2007 end-page: 2898 ident: CR34 article-title: Urinary excretion and blood level of prions in scrapie-infected hamsters publication-title: J. Gen. Virol. doi: 10.1099/vir.0.82786-0 – volume: 327 start-page: 1091 year: 2010 end-page: 1092 ident: CR27 article-title: Biochemistry. What makes a prion infectious? publication-title: Science doi: 10.1126/science.1187790 – volume: 31 start-page: 150 year: 2006 end-page: 155 ident: CR15 article-title: Amyloids, prions and the inherent infectious nature of misfolded protein aggregates publication-title: Trends Biochem. Sci. doi: 10.1016/j.tibs.2006.01.002 – volume: 121 start-page: 195 year: 2005 end-page: 206 ident: CR16 article-title: generation of infectious scrapie prions publication-title: Cell doi: 10.1016/j.cell.2005.02.011 – volume: 95 start-page: 13363 year: 1998 end-page: 13383 ident: CR1 article-title: Prions publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.95.23.13363 – volume: 5 start-page: e1000421 year: 2009 ident: CR30 article-title: generation of infectious prions produces a new disease phenotype publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1000421 – volume: 49 start-page: 3928 year: 2010 end-page: 3934 ident: CR28 article-title: Species-dependent differences in cofactor utilization for formation of the protease-resistant prion protein publication-title: Biochemistry doi: 10.1021/bi100370b – volume: 4 start-page: e4848 year: 2009 ident: CR40 article-title: Detection of CWD prions in urine and saliva of deer by transgenic mouse bioassay publication-title: PLoS ONE doi: 10.1371/journal.pone.0004848 – volume: 134 start-page: 757 year: 2008 end-page: 768 ident: CR29 article-title: Crossing the species barrier by PrP(Sc) replication generates unique infectious prions publication-title: Cell doi: 10.1016/j.cell.2008.07.030 – volume: 7 start-page: e1002370 year: 2011 ident: CR48 article-title: Ultraefficient PrPSc amplification highlights potentialities and pitfalls of the PMCA technology publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1002370 – volume: 364 start-page: 527 year: 2004 end-page: 529 ident: CR6 article-title: Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient publication-title: Lancet doi: 10.1016/S0140-6736(04)16811-6 – volume: 36 start-page: 151 year: 2011 end-page: 158 ident: CR8 article-title: Prion hypothesis: the end of the controversy? publication-title: Trends Biochem. Sci. doi: 10.1016/j.tibs.2010.11.001 – volume: 50 start-page: 996 year: 2010 end-page: 1002 ident: CR35 article-title: Discrimination between prion-infected and normal blood samples by protein misfolding cyclic amplification publication-title: Transfusion doi: 10.1111/j.1537-2995.2010.02595.x – volume: 3 start-page: 171 year: 2009 end-page: 183 ident: CR42 article-title: Detection of protease-resistant cervid prion protein in water from a CWD-endemic area publication-title: Prion doi: 10.4161/pri.3.3.9819 – volume: 7 start-page: e1001277 year: 2011 ident: CR18 article-title: Highly efficient protein misfolding cyclic amplification publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1001277 – volume: 397 start-page: 626 year: 2010 end-page: 630 ident: CR43 article-title: Sensitive detection of scrapie prion protein in soil publication-title: Biochem. Biophys. Res. Commun. doi: 10.1016/j.bbrc.2010.06.013 – volume: 77 start-page: 8462 year: 2003 end-page: 8469 ident: CR38 article-title: Evaluation of quinacrine treatment for prion diseases publication-title: J. Virol. doi: 10.1128/JVI.77.15.8462-8469.2003 – volume: 377 start-page: 373 year: 2008 end-page: 378 ident: CR39 article-title: Reduction of prion infectivity in packed red blood cells publication-title: Biochem. Biophys. Res. Commun. doi: 10.1016/j.bbrc.2008.09.141 – volume: 89 start-page: 3177 year: 2008 end-page: 3184 ident: CR49 article-title: amplification of PrPSc derived from the brain and blood of sheep infected with scrapie publication-title: J. Gen. Virol. doi: 10.1099/vir.0.2008/004226-0 – volume: 88 start-page: 2890 year: 2007 ident: BFnprot2012067_CR34 publication-title: J. Gen. Virol. doi: 10.1099/vir.0.82786-0 – volume: 11 start-page: 982 year: 2005 ident: BFnprot2012067_CR32 publication-title: Nat. Med. doi: 10.1038/nm1286 – volume: 382 start-page: 267 year: 2008 ident: BFnprot2012067_CR23 publication-title: Virology doi: 10.1016/j.virol.2008.09.023 – volume: 49 start-page: 3928 year: 2010 ident: BFnprot2012067_CR28 publication-title: Biochemistry doi: 10.1021/bi100370b – volume: 281 start-page: 35245 year: 2006 ident: BFnprot2012067_CR17 publication-title: J. Biol. Chem. doi: 10.1074/jbc.M603964200 – volume: 24 start-page: 519 year: 2001 ident: BFnprot2012067_CR2 publication-title: Annu. Rev. Neurosci. doi: 10.1146/annurev.neuro.24.1.519 – volume: 582 start-page: 3161 year: 2008 ident: BFnprot2012067_CR33 publication-title: FEBS Lett. doi: 10.1016/j.febslet.2008.08.003 – volume: 4 start-page: e4848 year: 2009 ident: BFnprot2012067_CR40 publication-title: PLoS ONE doi: 10.1371/journal.pone.0004848 – volume: 368 start-page: 2061 year: 2006 ident: BFnprot2012067_CR7 publication-title: Lancet doi: 10.1016/S0140-6736(06)69835-8 – volume: 134 start-page: 757 year: 2008 ident: BFnprot2012067_CR29 publication-title: Cell doi: 10.1016/j.cell.2008.07.030 – volume: 4 start-page: 200 year: 2010 ident: BFnprot2012067_CR19 publication-title: Curr. Chem. Biol. – volume: 6 start-page: e20384 year: 2011 ident: BFnprot2012067_CR20 publication-title: PLoS ONE doi: 10.1371/journal.pone.0020384 – volume: 25 start-page: 390 year: 2002 ident: BFnprot2012067_CR11 publication-title: Trends Neurosci. doi: 10.1016/S0166-2236(02)02195-1 – volume: 6 start-page: 127 year: 1996 ident: BFnprot2012067_CR13 publication-title: Brain Pathol. doi: 10.1111/j.1750-3639.1996.tb00796.x – volume: 7 start-page: e1002370 year: 2011 ident: BFnprot2012067_CR48 publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1002370 – volume: 363 start-page: 417 year: 2004 ident: BFnprot2012067_CR5 publication-title: Lancet doi: 10.1016/S0140-6736(04)15486-X – volume: 50 start-page: 996 year: 2010 ident: BFnprot2012067_CR35 publication-title: Transfusion doi: 10.1111/j.1537-2995.2010.02595.x – volume: 4 start-page: e7990 year: 2009 ident: BFnprot2012067_CR41 publication-title: PLoS ONE doi: 10.1371/journal.pone.0007990 – volume: 377 start-page: 373 year: 2008 ident: BFnprot2012067_CR39 publication-title: Biochem. Biophys. Res. Commun. doi: 10.1016/j.bbrc.2008.09.141 – volume: 4 start-page: e1000139 year: 2008 ident: BFnprot2012067_CR22 publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1000139 – volume: 327 start-page: 1132 year: 2010 ident: BFnprot2012067_CR25 publication-title: Science doi: 10.1126/science.1183748 – volume: 286 start-page: 7490 year: 2011 ident: BFnprot2012067_CR46 publication-title: J. Biol. Chem. doi: 10.1074/jbc.M110.198465 – volume: 349 start-page: 715 year: 1997 ident: BFnprot2012067_CR4 publication-title: Lancet doi: 10.1016/S0140-6736(96)08496-6 – volume: 2 start-page: 807 year: 1995 ident: BFnprot2012067_CR12 publication-title: Chem. Biol. doi: 10.1016/1074-5521(95)90087-X – volume: 584 start-page: 2409 year: 2010 ident: BFnprot2012067_CR26 publication-title: FEBS Lett. doi: 10.1016/j.febslet.2010.04.040 – volume: 413 start-page: 270 year: 2006 ident: BFnprot2012067_CR45 publication-title: Neurosci. Lett. doi: 10.1016/j.neulet.2006.11.056 – volume: 349 start-page: 636 year: 1997 ident: BFnprot2012067_CR3 publication-title: Lancet doi: 10.1016/S0140-6736(96)01310-4 – volume: 77 start-page: 8462 year: 2003 ident: BFnprot2012067_CR38 publication-title: J. Virol. doi: 10.1128/JVI.77.15.8462-8469.2003 – volume: 121 start-page: 195 year: 2005 ident: BFnprot2012067_CR16 publication-title: Cell doi: 10.1016/j.cell.2005.02.011 – volume: 7 start-page: 519 year: 2010 ident: BFnprot2012067_CR37 publication-title: Nat. Methods doi: 10.1038/nmeth.1465 – volume: 95 start-page: 13363 year: 1998 ident: BFnprot2012067_CR1 publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.95.23.13363 – volume: 5 start-page: e1000421 year: 2009 ident: BFnprot2012067_CR30 publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1000421 – volume: 7 start-page: e1001277 year: 2011 ident: BFnprot2012067_CR18 publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1001277 – volume: 313 start-page: 92 year: 2006 ident: BFnprot2012067_CR36 publication-title: Science doi: 10.1126/science.1129051 – volume: 104 start-page: 9741 year: 2007 ident: BFnprot2012067_CR24 publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.0702662104 – volume: 89 start-page: 3177 year: 2008 ident: BFnprot2012067_CR49 publication-title: J. Gen. Virol. doi: 10.1099/vir.0.2008/004226-0 – volume: 81 start-page: 9605 year: 2007 ident: BFnprot2012067_CR47 publication-title: J. Virol. doi: 10.1128/JVI.00635-07 – volume: 327 start-page: 1091 year: 2010 ident: BFnprot2012067_CR27 publication-title: Science doi: 10.1126/science.1187790 – volume: 364 start-page: 527 year: 2004 ident: BFnprot2012067_CR6 publication-title: Lancet doi: 10.1016/S0140-6736(04)16811-6 – volume: 73 start-page: 1055 year: 1993 ident: BFnprot2012067_CR14 publication-title: Cell doi: 10.1016/0092-8674(93)90635-4 – volume: 27 start-page: 2557 year: 2008 ident: BFnprot2012067_CR21 publication-title: EMBO J. doi: 10.1038/emboj.2008.181 – volume: 3 start-page: 171 year: 2009 ident: BFnprot2012067_CR42 publication-title: Prion doi: 10.4161/pri.3.3.9819 – volume: 36 start-page: 151 year: 2011 ident: BFnprot2012067_CR9 publication-title: Trends Mol. Med. – volume: 411 start-page: 810 year: 2001 ident: BFnprot2012067_CR10 publication-title: Nature doi: 10.1038/35081095 – volume: 2 start-page: 809 year: 2004 ident: BFnprot2012067_CR31 publication-title: Nat. Rev. Microbiol. doi: 10.1038/nrmicro1003 – volume: 36 start-page: 151 year: 2011 ident: BFnprot2012067_CR8 publication-title: Trends Biochem. Sci. doi: 10.1016/j.tibs.2010.11.001 – volume: 31 start-page: 150 year: 2006 ident: BFnprot2012067_CR15 publication-title: Trends Biochem. Sci. doi: 10.1016/j.tibs.2006.01.002 – volume: 397 start-page: 626 year: 2010 ident: BFnprot2012067_CR43 publication-title: Biochem. Biophys. Res. Commun. doi: 10.1016/j.bbrc.2010.06.013 – volume: 66 start-page: 2096 year: 1992 ident: BFnprot2012067_CR44 publication-title: J. Virol. doi: 10.1128/jvi.66.4.2096-2101.1992 – reference: 19436715 - PLoS Pathog. 2009 May;5(5):e1000421 – reference: 9811807 - Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13363-83 – reference: 17872544 - J Gen Virol. 2007 Oct;88(Pt 10):2890-8 – reference: 15378045 - Nat Rev Microbiol. 2004 Oct;2(10):809-19 – reference: 16982620 - J Biol Chem. 2006 Nov 17;281(46):35245-52 – reference: 20512142 - Nat Methods. 2010 Jul;7(7):519-20 – reference: 15302196 - Lancet. 2004 Aug 7-13;364(9433):527-9 – reference: 18800058 - EMBO J. 2008 Oct 8;27(19):2557-66 – reference: 14962520 - Lancet. 2004 Feb 7;363(9407):417-21 – reference: 20377181 - Biochemistry. 2010 May 11;49(18):3928-34 – reference: 21647368 - PLoS One. 2011;6(5):e20384 – reference: 1347795 - J Virol. 1992 Apr;66(4):2096-101 – reference: 17553879 - J Virol. 2007 Sep;81(17):9605-8 – reference: 21130657 - Trends Biochem Sci. 2011 Mar;36(3):151-8 – reference: 16473510 - Trends Biochem Sci. 2006 Mar;31(3):150-5 – reference: 12127750 - Trends Neurosci. 2002 Aug;25(8):390-4 – reference: 22114554 - PLoS Pathog. 2011 Nov;7(11):e1002370 – reference: 20570651 - Biochem Biophys Res Commun. 2010 Jul 2;397(3):626-30 – reference: 20110469 - Science. 2010 Feb 26;327(5969):1132-5 – reference: 16127436 - Nat Med. 2005 Sep;11(9):982-5 – reference: 8737929 - Brain Pathol. 1996 Apr;6(2):127-45 – reference: 18775309 - Cell. 2008 Sep 5;134(5):757-68 – reference: 20185716 - Science. 2010 Feb 26;327(5969):1091-2 – reference: 19823039 - Prion. 2009 Jul-Sep;3(3):171-83 – reference: 19008409 - J Gen Virol. 2008 Dec;89(Pt 12):3177-84 – reference: 21209079 - J Biol Chem. 2011 Mar 4;286(9):7490-5 – reference: 11459061 - Nature. 2001 Jun 14;411(6839):810-3 – reference: 18706416 - FEBS Lett. 2008 Sep 22;582(21-22):3161-6 – reference: 17161728 - Lancet. 2006 Dec 9;368(9552):2061-7 – reference: 17174030 - Neurosci Lett. 2007 Feb 21;413(3):270-3 – reference: 18769716 - PLoS Pathog. 2008;4(8):e1000139 – reference: 9057745 - Lancet. 1997 Mar 1;349(9052):636-41 – reference: 15851027 - Cell. 2005 Apr 22;121(2):195-206 – reference: 18851948 - Biochem Biophys Res Commun. 2008 Dec 12;377(2):373-8 – reference: 8807814 - Chem Biol. 1995 Dec;2(12):807-17 – reference: 9078212 - Lancet. 1997 Mar 8;349(9053):715-21 – reference: 12857915 - J Virol. 2003 Aug;77(15):8462-9 – reference: 20412808 - FEBS Lett. 2010 Jun 3;584(11):2409-14 – reference: 19293928 - PLoS One. 2009;4(3):e4848 – reference: 8513491 - Cell. 1993 Jun 18;73(6):1055-8 – reference: 17535913 - Proc Natl Acad Sci U S A. 2007 Jun 5;104(23):9741-6 – reference: 18952250 - Virology. 2008 Dec 20;382(2):267-76 – reference: 16825570 - Science. 2006 Jul 7;313(5783):92-4 – reference: 19956732 - PLoS One. 2009;4(11):e7990 – reference: 21347353 - PLoS Pathog. 2011;7(2):e1001277 – reference: 20180925 - Transfusion. 2010 May;50(5):996-1002 – reference: 11283320 - Annu Rev Neurosci. 2001;24:519-50 – reference: 20889378 - Trends Mol Med. 2011 Jan;17(1):14-24 |
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Snippet | Prions are proteinaceous infectious agents responsible for the transmission of prion diseases. The lack of a procedure for cultivating prions in the laboratory... |
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SubjectTerms | 631/1647/2196 64 64/110 692/699/375/1937 82 Alzheimer's disease Amplification Analytical Chemistry Biological Techniques Blood Blood & organ donations Brain research Computational Biology/Bioinformatics Disease Disease transmission Food industry Food safety Humans In vivo methods and tests Infectivity Life Sciences Microarrays Organic Chemistry Polymers Prion Diseases - genetics Prion protein Prions Prions - chemistry Protein Engineering - methods Protein Folding Protein Multimerization Proteins Protocol Replication Seeds Sonication Sonication - methods Ultrasonic imaging Veterinary diseases |
Title | Protein misfolding cyclic amplification of infectious prions |
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