TY - JOUR
T1 - Closing and opening of the RNA polymerase trigger loop
AU - Mazumder, Abhishek
AU - Lin, Miaoxin
AU - Kapanidis, Achillefs N.
AU - Ebright, Richard H.
N1 - Funding Information:
ACKNOWLEDGMENTS. R.H.E. was supported by NIH Grant GM041376. A.N.K. was supported by Wellcome Trust Grant 110164/Z/15/Z, and UK Biotechnology and Biological Sciences Research Council Grants BB/H01795X/1 and BB/ J00054X/1. We thank W. Fenical and E. Steinbrecher for compounds.
Publisher Copyright:
© 2020 National Academy of Sciences. All rights reserved.
PY - 2020/7/7
Y1 - 2020/7/7
N2 - The RNA polymerase (RNAP) trigger loop (TL) is a mobile structural element of the RNAP active center that, based on crystal structures, has been proposed to cycle between an “unfolded”/“open” state that allows an NTP substrate to enter the active center and a “folded”/“closed” state that holds the NTP substrate in the active center. Here, by quantifying single-molecule fluorescence resonance energy transfer between a first fluorescent probe in the TL and a second fluorescent probe elsewhere in RNAP or in DNA, we detect and characterize TL closing and opening in solution. We show that the TL closes and opens on the millisecond timescale; we show that TL closing and opening provides a checkpoint for NTP complementarity, NTP ribo/deoxyribo identity, and NTP tri/di/ monophosphate identity, and serves as a target for inhibitors; and we show that one cycle of TL closing and opening typically occurs in each nucleotide addition cycle in transcription elongation.
AB - The RNA polymerase (RNAP) trigger loop (TL) is a mobile structural element of the RNAP active center that, based on crystal structures, has been proposed to cycle between an “unfolded”/“open” state that allows an NTP substrate to enter the active center and a “folded”/“closed” state that holds the NTP substrate in the active center. Here, by quantifying single-molecule fluorescence resonance energy transfer between a first fluorescent probe in the TL and a second fluorescent probe elsewhere in RNAP or in DNA, we detect and characterize TL closing and opening in solution. We show that the TL closes and opens on the millisecond timescale; we show that TL closing and opening provides a checkpoint for NTP complementarity, NTP ribo/deoxyribo identity, and NTP tri/di/ monophosphate identity, and serves as a target for inhibitors; and we show that one cycle of TL closing and opening typically occurs in each nucleotide addition cycle in transcription elongation.
KW - Conformational dynamics
KW - RNA polymerase
KW - Single-molecule fluorescence resonance energy transfer
KW - Transcription
KW - Trigger loop
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U2 - 10.1073/pnas.1920427117
DO - 10.1073/pnas.1920427117
M3 - Article
C2 - 32571927
AN - SCOPUS:85088210120
SN - 0027-8424
VL - 117
SP - 15642
EP - 15649
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 27
ER -