TY - JOUR
T1 - Protein misfolding cyclic amplification of infectious prions.
AU - Morales, Rodrigo
AU - Duran-Aniotz, Claudia
AU - Diaz-Espinoza, Rodrigo
AU - Camacho, Manuel V.
AU - Soto, Claudio
N1 - Funding Information:
acknowleDGMents We thank the many former laboratory members whose input has been important for reaching the optimal PMCA procedure, especially G. Saborio, L. Anderes, C. Adessi, K. Maundrell, J. Castilla, P. Saa, K. Abid, M. Barria, D. Gonzalez-Romero and B. Chen. We also thank M.-J. Liberona for critical reading of the manuscript. This work was partially supported by US National Institutes of Health grants R01 NS049173, P01 AI077774 and P01 AG014359 to C.S.
PY - 2012/7
Y1 - 2012/7
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84866789585&partnerID=8YFLogxK
U2 - 10.1038/nprot.2012.067
DO - 10.1038/nprot.2012.067
M3 - Article
C2 - 22743831
AN - SCOPUS:84866789585
SN - 1750-2799
VL - 7
SP - 1397
EP - 1409
JO - Nature protocols
JF - Nature protocols
IS - 7
ER -