TY - JOUR
T1 - Cryo-EM in the study of challenging systems
T2 - the human transcription pre-initiation complex
AU - Nogales, Eva
AU - Louder, Robert K.
AU - He, Yuan
N1 - Funding Information:
This work was funded by NIGMS (GM63072 to EN). EN is a Howard Hughes Medical Institute Investigator.
Publisher Copyright:
© 2016
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Single particle cryo-Electron Microscopy (cryo-EM) is a technique that allows the structural characterization of macromolecules without the need for crystallization. For certain type of samples that are ideally suited for cryo-EM studies it has been possible to reach high-resolution structures following relatively standard procedures. Other biological systems remain highly challenging, even for cryo-EM. Challenges may involve the scarcity of the sample, poor stability of the complexes, and most often, the intrinsic flexibility of biological molecules. Among these challenging samples are large eukaryotic transcription complexes, which suffer from all such shortcomings. Here we report how we have recently tried to overcome those challenges in order to improve our structural understanding of the human transcription pre-initiation complex assembly and the transcription initiation process. Parallel efforts have also been carried out for budding yeast transcription initiation complexes, allowing comparisons that establish both the overall conservation and the specific structural differences between the two systems.
AB - Single particle cryo-Electron Microscopy (cryo-EM) is a technique that allows the structural characterization of macromolecules without the need for crystallization. For certain type of samples that are ideally suited for cryo-EM studies it has been possible to reach high-resolution structures following relatively standard procedures. Other biological systems remain highly challenging, even for cryo-EM. Challenges may involve the scarcity of the sample, poor stability of the complexes, and most often, the intrinsic flexibility of biological molecules. Among these challenging samples are large eukaryotic transcription complexes, which suffer from all such shortcomings. Here we report how we have recently tried to overcome those challenges in order to improve our structural understanding of the human transcription pre-initiation complex assembly and the transcription initiation process. Parallel efforts have also been carried out for budding yeast transcription initiation complexes, allowing comparisons that establish both the overall conservation and the specific structural differences between the two systems.
UR - http://www.scopus.com/inward/record.url?scp=84988884528&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84988884528&partnerID=8YFLogxK
U2 - 10.1016/j.sbi.2016.09.009
DO - 10.1016/j.sbi.2016.09.009
M3 - Review article
C2 - 27689812
AN - SCOPUS:84988884528
SN - 0959-440X
VL - 40
SP - 120
EP - 127
JO - Current Opinion in Structural Biology
JF - Current Opinion in Structural Biology
ER -