Real-Time Monitoring of Chromophore Isomerization and Deprotonation during the Photoactivation of the Fluorescent Protein Dronpa

Dronpa is a photochromic green fluorescent protein (GFP) homologue used as a probe in super-resolution microscopy. It is known that the photochromic reaction involves cis/trans isomerization of the chromophore and protonation/deprotonation of its phenol group, but the sequence in time of the two ste...

Full description

Saved in:
Bibliographic Details
Published inThe journal of physical chemistry. B Vol. 119; no. 6; pp. 2404 - 2414
Main Authors Yadav, Dheerendra, Lacombat, Fabien, Dozova, Nadia, Rappaport, Fabrice, Plaza, Pascal, Espagne, Agathe
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 12.02.2015
SeriesPhotoinduced Proton Transfer in Chemistry and Biology
Subjects
Online AccessGet full text
ISSN1520-6106
1520-5207
1520-5207
DOI10.1021/jp507094f

Cover

Abstract Dronpa is a photochromic green fluorescent protein (GFP) homologue used as a probe in super-resolution microscopy. It is known that the photochromic reaction involves cis/trans isomerization of the chromophore and protonation/deprotonation of its phenol group, but the sequence in time of the two steps and their characteristic time scales are still the subject of much debate. We report here a comprehensive UV–visible transient absorption spectroscopy study of the photoactivation mechanism of Dronpa, covering all relevant time scales from ∼100 fs to milliseconds. The Dronpa-2 variant was also studied and showed the same behavior. By carefully controlling the excitation energy to avoid multiphoton processes, we could measure both the spectrum and the anisotropy of the first photoactivation intermediate. We show that the observed few nanometer blue-shift of this intermediate is characteristic for a neutral cis chromophore, and that its anisotropy of ∼0.2 is in good agreement with the reorientation of the transition dipole moment expected upon isomerization. These data constitute the first clear evidence that trans → cis isomerization of the chromophore precedes its deprotonation and occurs on the picosecond time scale, concomitantly to the excited-state decay. We found the deprotonation step to follow in ∼10 μs and lead directly from the neutral cis intermediate to the final state.
AbstractList Dronpa is a photochromic green fluorescent protein (GFP) homologue used as a probe in super-resolution microscopy. It is known that the photochromic reaction involves cis/trans isomerization of the chromophore and protonation/deprotonation of its phenol group, but the sequence in time of the two steps and their characteristic time scales are still the subject of much debate. We report here a comprehensive UV–visible transient absorption spectroscopy study of the photoactivation mechanism of Dronpa, covering all relevant time scales from ∼100 fs to milliseconds. The Dronpa-2 variant was also studied and showed the same behavior. By carefully controlling the excitation energy to avoid multiphoton processes, we could measure both the spectrum and the anisotropy of the first photoactivation intermediate. We show that the observed few nanometer blue-shift of this intermediate is characteristic for a neutral cis chromophore, and that its anisotropy of ∼0.2 is in good agreement with the reorientation of the transition dipole moment expected upon isomerization. These data constitute the first clear evidence that trans → cis isomerization of the chromophore precedes its deprotonation and occurs on the picosecond time scale, concomitantly to the excited-state decay. We found the deprotonation step to follow in ∼10 μs and lead directly from the neutral cis intermediate to the final state.
Dronpa is a photochromic green fluorescent protein (GFP) homologue used as a probe in super-resolution microscopy. It is known that the photochromic reaction involves cis/trans isomerization of the chromophore and protonation/deprotonation of its phenol group, but the sequence in time of the two steps and their characteristic time scales are still the subject of much debate. We report here a comprehensive UV-visible transient absorption spectroscopy study of the photoactivation mechanism of Dronpa, covering all relevant time scales from ∼100 fs to milliseconds. The Dronpa-2 variant was also studied and showed the same behavior. By carefully controlling the excitation energy to avoid multiphoton processes, we could measure both the spectrum and the anisotropy of the first photoactivation intermediate. We show that the observed few nanometer blue-shift of this intermediate is characteristic for a neutral cis chromophore, and that its anisotropy of ∼0.2 is in good agreement with the reorientation of the transition dipole moment expected upon isomerization. These data constitute the first clear evidence that trans → cis isomerization of the chromophore precedes its deprotonation and occurs on the picosecond time scale, concomitantly to the excited-state decay. We found the deprotonation step to follow in ∼10 μs and lead directly from the neutral cis intermediate to the final state.Dronpa is a photochromic green fluorescent protein (GFP) homologue used as a probe in super-resolution microscopy. It is known that the photochromic reaction involves cis/trans isomerization of the chromophore and protonation/deprotonation of its phenol group, but the sequence in time of the two steps and their characteristic time scales are still the subject of much debate. We report here a comprehensive UV-visible transient absorption spectroscopy study of the photoactivation mechanism of Dronpa, covering all relevant time scales from ∼100 fs to milliseconds. The Dronpa-2 variant was also studied and showed the same behavior. By carefully controlling the excitation energy to avoid multiphoton processes, we could measure both the spectrum and the anisotropy of the first photoactivation intermediate. We show that the observed few nanometer blue-shift of this intermediate is characteristic for a neutral cis chromophore, and that its anisotropy of ∼0.2 is in good agreement with the reorientation of the transition dipole moment expected upon isomerization. These data constitute the first clear evidence that trans → cis isomerization of the chromophore precedes its deprotonation and occurs on the picosecond time scale, concomitantly to the excited-state decay. We found the deprotonation step to follow in ∼10 μs and lead directly from the neutral cis intermediate to the final state.
Dronpa is a GFP-related photochromic fluorescent protein used as probe in superresolution microscopy. It is known that the photochromic reaction involves cis/trans isomerization of the chromophore and protonation/deprotonation of its phenol group, but the sequence in time of the two steps and their characteristic timescales are still the subject of much debate. We report here a comprehensive UV-visible transient absorption spectroscopy study of the photoactivation mechanism of Dronpa, covering all relevant timescales from ~100 fs to milliseconds. The Dronpa-2 variant was also studied and showed the same behavior. By carefully controlling the excitation energy to avoid multiphoton processes, we could measure both the spectrum and the anisotropy of the first photoactivation intermediate. We show that the observed few nanometer blue-shift of this intermediate is characteristic for a neutral cis chromophore, and that its anisotropy of ~0.2 is in good agreement with the reorientation of the transition dipole moment expected upon isomerization. These data constitute the first clear evidence that trans→cis isomerization of the chromophore precedes its deprotonation and occurs on the picosecond timescale, concomitantly to the excited-state decay. We found the deprotonation step to follow in ~10 μs and lead directly from the neutral cis intermediate to the final state.
Author Espagne, Agathe
Plaza, Pascal
Yadav, Dheerendra
Dozova, Nadia
Lacombat, Fabien
Rappaport, Fabrice
AuthorAffiliation Ecole Normale Supérieure-PSL Research University
Institut de Biologie Physico-Chimique
Département de Chimie
CNRS, UMR 8640 PASTEUR
UMR 7141 CNRS-UPMC
Sorbonne Universités, UPMC Univ Paris 06, PASTEUR
AuthorAffiliation_xml – name: Institut de Biologie Physico-Chimique
– name: Département de Chimie
– name: Ecole Normale Supérieure-PSL Research University
– name: CNRS, UMR 8640 PASTEUR
– name: UMR 7141 CNRS-UPMC
– name: Sorbonne Universités, UPMC Univ Paris 06, PASTEUR
Author_xml – sequence: 1
  givenname: Dheerendra
  surname: Yadav
  fullname: Yadav, Dheerendra
– sequence: 2
  givenname: Fabien
  surname: Lacombat
  fullname: Lacombat, Fabien
– sequence: 3
  givenname: Nadia
  surname: Dozova
  fullname: Dozova, Nadia
– sequence: 4
  givenname: Fabrice
  surname: Rappaport
  fullname: Rappaport, Fabrice
– sequence: 5
  givenname: Pascal
  surname: Plaza
  fullname: Plaza, Pascal
– sequence: 6
  givenname: Agathe
  surname: Espagne
  fullname: Espagne, Agathe
  email: agathe.espagne@ens.fr
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25325882$$D View this record in MEDLINE/PubMed
https://hal.science/hal-03499998$$DView record in HAL
BookMark eNqFkV1rFDEUhoNU7Ide-AckN0K9GJuPSWZyWbbWFlYsUq9DduaMk2UmGZNMQa_86WY76wpSMBByePO8h_Nxio6cd4DQa0reU8LoxXYSpCKq7J6hEyoYKfKtjvaxpEQeo9MYt4QwwWr5Ah0zwZmoa3aCfn0BMxT3dgT8yTubfLDuG_YdXvXBj37qfQB8G_0Iwf40yXqHjWvxFUzBJ-8WpZ0fXakHfNdn2TTJPixfOdNOvh7mnCg24BK-y06wDl8F7ybzEj3vzBDh1f49Q1-vP9yvbor154-3q8t1Ycqap0K1HWmYArGpFW9L1takVJI1uaGyAdkaupEVZyAoN8AAOtjImrW0ERU3kgM_Q--WvL0Z9BTsaMIP7Y3VN5drvdMIL1U-9QPN7PnC5ia_zxCTHm2ufRiMAz9HzQghgiiu1H9RKoVgQlVMZvTNHp03I7SHIv4s42-JTfAxBugOCCV6t2h9WHRmL_5hG5seR56CscOTjreLwzRRb_0cXB73E9xvOcW2_A
CitedBy_id crossref_primary_10_1080_10408347_2021_1907735
crossref_primary_10_1038_s41467_017_00847_3
crossref_primary_10_1021_acs_chemrev_6b00238
crossref_primary_10_1021_acs_jpclett_7b00348
crossref_primary_10_1038_s41467_020_14537_0
crossref_primary_10_1007_s43630_021_00048_4
crossref_primary_10_1371_journal_pone_0123338
crossref_primary_10_1021_acs_jpclett_6b02816
crossref_primary_10_1039_D3CC01617J
crossref_primary_10_1038_s41557_018_0073_0
crossref_primary_10_1007_s40766_024_00052_1
crossref_primary_10_1016_j_jmb_2016_02_029
crossref_primary_10_1021_acs_jpclett_4c03651
crossref_primary_10_1021_acs_jpcb_2c06780
crossref_primary_10_1002_ange_201508452
crossref_primary_10_1073_pnas_1618087114
crossref_primary_10_1063_1_5043246
crossref_primary_10_1021_acs_jpcb_6b10859
crossref_primary_10_1088_0953_8984_28_44_443001
crossref_primary_10_1021_acs_jpclett_3c00431
crossref_primary_10_1021_acs_jpcb_6b05795
crossref_primary_10_1021_acs_jpcb_6b01752
crossref_primary_10_1063_1_4979844
crossref_primary_10_1021_acs_jpcb_1c08570
crossref_primary_10_3390_ijms18061187
crossref_primary_10_1021_acs_jpclett_5b02789
crossref_primary_10_1002_cptc_201700002
crossref_primary_10_1002_pro_4517
crossref_primary_10_3390_ijms23126459
crossref_primary_10_1021_acs_jpcb_5b04826
crossref_primary_10_1038_nchem_2853
crossref_primary_10_1039_C8FD00058A
crossref_primary_10_1002_anie_201508452
crossref_primary_10_1021_acs_jpclett_3c00165
Cites_doi 10.1021/bi1015875
10.1351/pac200476122105
10.1021/jp037902h
10.1073/pnas.0500489102
10.1021/jp047465m
10.1016/S0006-3495(00)76711-7
10.1073/pnas.0404262102
10.1021/ja078193e
10.1073/pnas.0502772102
10.1038/ncomms2460
10.1126/science.1102506
10.1021/ja0520520
10.1016/S0301-0104(96)00340-0
10.1021/jp111593x
10.1021/jp0709104
10.1021/jp909947c
10.1063/1.372185
10.1021/cr00003a007
10.1063/1.1149566
10.1021/jz3008408
10.1016/0040-4039(70)80027-2
10.1073/pnas.0506010102
10.1074/jbc.M109.086314
10.1016/j.jmb.2006.08.089
10.1021/jp802419h
10.1021/jp406142g
10.1021/ja803416h
10.1021/bi901562a
10.1007/978-0-387-46312-4_10
10.1073/pnas.0709599105
10.1073/pnas.0808882105
10.1073/pnas.0700629104
10.1073/pnas.93.16.8362
10.1073/pnas.93.24.13617
10.1073/pnas.1204917109
10.1042/BJ20061401
10.1039/c2cp23351g
10.1021/ja207001y
10.1529/biophysj.107.105882
10.1126/science.1127344
10.1021/ja069365v
10.1016/j.chembiol.2010.05.022
10.1021/jp110741y
10.1073/pnas.0700059104
10.1073/pnas.1000001107
ContentType Journal Article
Copyright Copyright © 2014 American Chemical Society
Distributed under a Creative Commons Attribution 4.0 International License
Copyright_xml – notice: Copyright © 2014 American Chemical Society
– notice: Distributed under a Creative Commons Attribution 4.0 International License
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7S9
L.6
1XC
VOOES
DOI 10.1021/jp507094f
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
Hyper Article en Ligne (HAL)
Hyper Article en Ligne (HAL) (Open Access)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
DatabaseTitleList AGRICOLA
MEDLINE - Academic
MEDLINE


Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1520-5207
EndPage 2414
ExternalDocumentID oai_HAL_hal_03499998v1
25325882
10_1021_jp507094f
c634541424
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID -
.K2
02
123
29L
4.4
53G
55A
5VS
7~N
85S
8RP
AABXI
ABFLS
ABMVS
ABPTK
ABUCX
ACGFS
ACNCT
ACS
AEESW
AENEX
AFEFF
ALMA_UNASSIGNED_HOLDINGS
AQSVZ
BAANH
CS3
DU5
EBS
ED
ED~
EJD
F20
F5P
GNL
IH9
IHE
JG
JG~
K2
LG6
PZZ
RNS
ROL
TAE
TN5
UI2
UKR
UPT
VF5
VG9
VQA
W1F
WH7
X
YZZ
ZGI
ZHY
---
-~X
.DC
AAHBH
AAYXX
ABBLG
ABJNI
ABLBI
ABQRX
ACBEA
ADHLV
AHGAQ
CITATION
CUPRZ
GGK
XSW
YQT
~02
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7S9
L.6
186
1XC
6TJ
9M8
ABDPE
ACRPL
ADNMO
AETEA
AEYZD
AFFNX
AGQPQ
AI.
ANPPW
ANTXH
MVM
NHB
UQL
VH1
VOH
VOOES
VQP
ZCG
ID FETCH-LOGICAL-a483t-9df0c29e5b893d42d804962c5284ce6da1b6732e513ae2eefeb682d1c573a63e3
IEDL.DBID ACS
ISSN 1520-6106
1520-5207
IngestDate Fri Sep 12 12:49:43 EDT 2025
Fri Jul 11 09:52:04 EDT 2025
Fri Jul 11 06:53:30 EDT 2025
Mon Jul 21 06:06:58 EDT 2025
Tue Jul 01 00:22:03 EDT 2025
Thu Apr 24 23:02:22 EDT 2025
Thu Aug 27 13:42:11 EDT 2020
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords Green Fluorescent Protein
proton transfer
photochromism
femtosecond UV-visible spectroscopy
nanosecond UV-visible spectroscopy
cis/trans photoisomerization
Language English
License Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a483t-9df0c29e5b893d42d804962c5284ce6da1b6732e513ae2eefeb682d1c573a63e3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-8021-4521
OpenAccessLink https://hal.science/hal-03499998
PMID 25325882
PQID 1655259726
PQPubID 23479
PageCount 11
ParticipantIDs hal_primary_oai_HAL_hal_03499998v1
proquest_miscellaneous_2000509399
proquest_miscellaneous_1655259726
pubmed_primary_25325882
crossref_primary_10_1021_jp507094f
crossref_citationtrail_10_1021_jp507094f
acs_journals_10_1021_jp507094f
ProviderPackageCode JG~
55A
AABXI
GNL
VF5
7~N
VG9
W1F
ACS
AEESW
AFEFF
.K2
ABMVS
ABUCX
IH9
BAANH
AQSVZ
ED~
UI2
CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2015-02-12
PublicationDateYYYYMMDD 2015-02-12
PublicationDate_xml – month: 02
  year: 2015
  text: 2015-02-12
  day: 12
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationSeriesTitle Photoinduced Proton Transfer in Chemistry and Biology
PublicationTitle The journal of physical chemistry. B
PublicationTitleAlternate J. Phys. Chem. B
PublicationYear 2015
Publisher American Chemical Society
Publisher_xml – name: American Chemical Society
References Espagne A. (ref22/cit22) 2011; 50
Ekvall K. (ref29/cit29) 2000; 87
Habuchi S. (ref19/cit19) 2005; 102
Förster T. (ref35/cit35) 1950; 54
Abbyad P. (ref43/cit43) 2007; 111
Marriott G. (ref6/cit6) 2008; 105
Cox R. J. (ref25/cit25) 1970
Kuhn H. J. (ref26/cit26) 2004; 76
Henderson J. N. (ref10/cit10) 2007; 104
Warren M. M. (ref17/cit17) 2013; 4
Chattoraj M. (ref20/cit20) 1996; 93
Brazard J. (ref28/cit28) 2011; 115
Addison K. (ref33/cit33) 2012; 3
Hofmann M. (ref1/cit1) 2005; 102
Agmon N. (ref37/cit37) 2005; 109
Wilmann P. G. (ref12/cit12) 2006; 364
Olsen S. (ref44/cit44) 2008; 130
Ando R. (ref21/cit21) 2007; 92
Conyard J. (ref40/cit40) 2011; 115
Andresen M. (ref7/cit7) 2005; 102
Dedecker P. (ref3/cit3) 2012; 109
Fron E. (ref16/cit16) 2007; 129
Li X. (ref15/cit15) 2010; 114
Usman A. (ref46/cit46) 2005; 127
Voliani V. (ref24/cit24) 2008; 112
Béal D. (ref32/cit32) 1999; 70
Dong J. (ref34/cit34) 2008; 130
Volkmer A. (ref31/cit31) 2000; 78
Lukacs A. (ref18/cit18) 2013; 117
Chang C. W. (ref42/cit42) 2010; 107
Thiagarajan V. (ref27/cit27) 2010; 49
Kennis J. T. (ref38/cit38) 2004; 101
Betzig E. (ref2/cit2) 2006; 313
Brakemann T. (ref9/cit9) 2010; 285
Andresen M. (ref8/cit8) 2007; 104
Subach F. V. (ref5/cit5) 2010; 17
Regis Faro A. (ref11/cit11) 2011; 133
Vengris M. (ref47/cit47) 2004; 108
Niwa H. (ref23/cit23) 1996; 93
Ansbacher T. (ref45/cit45) 2012; 14
Ando R. (ref4/cit4) 2004; 306
ref30/cit30
Waldeck D. H. (ref41/cit41) 1991; 91
Lossau H. (ref36/cit36) 1996; 213
Stiel A. C. (ref13/cit13) 2007; 402
Mizuno H. (ref14/cit14) 2008; 105
References_xml – volume: 50
  start-page: 437
  year: 2011
  ident: ref22/cit22
  publication-title: Biochemistry
  doi: 10.1021/bi1015875
– volume: 76
  start-page: 2105
  year: 2004
  ident: ref26/cit26
  publication-title: Pure Appl. Chem.
  doi: 10.1351/pac200476122105
– volume: 108
  start-page: 4587
  year: 2004
  ident: ref47/cit47
  publication-title: J. Phys. Chem. A
  doi: 10.1021/jp037902h
– volume: 102
  start-page: 9511
  year: 2005
  ident: ref19/cit19
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0500489102
– volume: 109
  start-page: 13
  year: 2005
  ident: ref37/cit37
  publication-title: J. Phys. Chem. A
  doi: 10.1021/jp047465m
– volume: 78
  start-page: 1589
  year: 2000
  ident: ref31/cit31
  publication-title: Biophys. J.
  doi: 10.1016/S0006-3495(00)76711-7
– volume: 101
  start-page: 17988
  year: 2004
  ident: ref38/cit38
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0404262102
– volume: 130
  start-page: 8677
  year: 2008
  ident: ref44/cit44
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja078193e
– volume: 102
  start-page: 13070
  year: 2005
  ident: ref7/cit7
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0502772102
– volume: 4
  start-page: 1461
  year: 2013
  ident: ref17/cit17
  publication-title: Nat. Commun.
  doi: 10.1038/ncomms2460
– volume: 54
  start-page: 42
  year: 1950
  ident: ref35/cit35
  publication-title: Z. Elektrochem.
– volume: 306
  start-page: 1370
  year: 2004
  ident: ref4/cit4
  publication-title: Science
  doi: 10.1126/science.1102506
– volume: 127
  start-page: 11214
  year: 2005
  ident: ref46/cit46
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja0520520
– volume: 213
  start-page: 1
  year: 1996
  ident: ref36/cit36
  publication-title: Chem. Phys.
  doi: 10.1016/S0301-0104(96)00340-0
– volume: 115
  start-page: 1571
  year: 2011
  ident: ref40/cit40
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp111593x
– volume: 111
  start-page: 8269
  year: 2007
  ident: ref43/cit43
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp0709104
– volume: 114
  start-page: 1114
  year: 2010
  ident: ref15/cit15
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp909947c
– volume: 87
  start-page: 2340
  year: 2000
  ident: ref29/cit29
  publication-title: J. Appl. Phys.
  doi: 10.1063/1.372185
– volume: 91
  start-page: 415
  year: 1991
  ident: ref41/cit41
  publication-title: Chem. Rev.
  doi: 10.1021/cr00003a007
– volume: 70
  start-page: 202
  year: 1999
  ident: ref32/cit32
  publication-title: Rev. Sci. Instrum.
  doi: 10.1063/1.1149566
– volume: 3
  start-page: 2298
  year: 2012
  ident: ref33/cit33
  publication-title: J. Phys. Chem. Lett.
  doi: 10.1021/jz3008408
– start-page: 207
  year: 1970
  ident: ref25/cit25
  publication-title: Tetrahedron Lett.
  doi: 10.1016/0040-4039(70)80027-2
– volume: 102
  start-page: 17565
  year: 2005
  ident: ref1/cit1
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0506010102
– volume: 285
  start-page: 14603
  year: 2010
  ident: ref9/cit9
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M109.086314
– volume: 364
  start-page: 213
  year: 2006
  ident: ref12/cit12
  publication-title: J. Mol. Biol.
  doi: 10.1016/j.jmb.2006.08.089
– volume: 112
  start-page: 10714
  year: 2008
  ident: ref24/cit24
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp802419h
– volume: 117
  start-page: 11954
  year: 2013
  ident: ref18/cit18
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp406142g
– volume: 130
  start-page: 14096
  year: 2008
  ident: ref34/cit34
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja803416h
– volume: 49
  start-page: 297
  year: 2010
  ident: ref27/cit27
  publication-title: Biochemistry
  doi: 10.1021/bi901562a
– ident: ref30/cit30
  doi: 10.1007/978-0-387-46312-4_10
– volume: 105
  start-page: 9227
  year: 2008
  ident: ref14/cit14
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0709599105
– volume: 105
  start-page: 17789
  year: 2008
  ident: ref6/cit6
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0808882105
– volume: 104
  start-page: 13005
  year: 2007
  ident: ref8/cit8
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0700629104
– volume: 93
  start-page: 8362
  year: 1996
  ident: ref20/cit20
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.93.16.8362
– volume: 93
  start-page: 13617
  year: 1996
  ident: ref23/cit23
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.93.24.13617
– volume: 109
  start-page: 10909
  year: 2012
  ident: ref3/cit3
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.1204917109
– volume: 402
  start-page: 35
  year: 2007
  ident: ref13/cit13
  publication-title: Biochem. J.
  doi: 10.1042/BJ20061401
– volume: 14
  start-page: 4109
  year: 2012
  ident: ref45/cit45
  publication-title: Phys. Chem. Chem. Phys.
  doi: 10.1039/c2cp23351g
– volume: 133
  start-page: 16362
  year: 2011
  ident: ref11/cit11
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja207001y
– volume: 92
  start-page: L97
  year: 2007
  ident: ref21/cit21
  publication-title: Biophys. J.
  doi: 10.1529/biophysj.107.105882
– volume: 313
  start-page: 1642
  year: 2006
  ident: ref2/cit2
  publication-title: Science
  doi: 10.1126/science.1127344
– volume: 129
  start-page: 4870
  year: 2007
  ident: ref16/cit16
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja069365v
– volume: 17
  start-page: 745
  year: 2010
  ident: ref5/cit5
  publication-title: Chem. Biol.
  doi: 10.1016/j.chembiol.2010.05.022
– volume: 115
  start-page: 3251
  year: 2011
  ident: ref28/cit28
  publication-title: J. Phys. Chem. A
  doi: 10.1021/jp110741y
– volume: 104
  start-page: 6672
  year: 2007
  ident: ref10/cit10
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.0700059104
– volume: 107
  start-page: 2914
  year: 2010
  ident: ref42/cit42
  publication-title: Proc. Natl. Acad. Sci. U.S.A.
  doi: 10.1073/pnas.1000001107
SSID ssj0025286
Score 2.3283205
Snippet Dronpa is a photochromic green fluorescent protein (GFP) homologue used as a probe in super-resolution microscopy. It is known that the photochromic reaction...
Dronpa is a GFP-related photochromic fluorescent protein used as probe in superresolution microscopy. It is known that the photochromic reaction involves...
SourceID hal
proquest
pubmed
crossref
acs
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 2404
SubjectTerms Chemical Sciences
energy
green fluorescent protein
Green Fluorescent Proteins - chemistry
isomerization
microscopy
Models, Molecular
monitoring
or physical chemistry
phenol
physical chemistry
Protein Conformation
Protons
spectroscopy
Stereoisomerism
Theoretical and
Ultraviolet Rays
Title Real-Time Monitoring of Chromophore Isomerization and Deprotonation during the Photoactivation of the Fluorescent Protein Dronpa
URI http://dx.doi.org/10.1021/jp507094f
https://www.ncbi.nlm.nih.gov/pubmed/25325882
https://www.proquest.com/docview/1655259726
https://www.proquest.com/docview/2000509399
https://hal.science/hal-03499998
Volume 119
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1Lb9QwEB71cYALtOW1UCpTOHBJGzuxkxyr3a4WRKsKqNRb5PihBUqy2geHnvrTmYk3KxBdmqMzcRyPnfnG4_kM8C4rrMsyYyKnlIlSH-eRFoWMcs-LwhrLTbuYc3auRpfpxyt5tQFv10TwBT_-PkHIgk6I34RtodC-EP7pf1l5VVK0xzmiHSI_KFYdfdCfj5LpMbO_TM_mmDY-rkOVrXUZPoZBl6MTNpX8OFrMqyNz8y9l4_8avgOPluiSnYThsAsbrt6DB_3uULcncPsZgWFEeR8szGZa1mONZ0SS-7OZjJupYx9mDcVxQoIm07VlA0d8Dk1YOWQhtZEhdGQXYyym3Iiwsks1UfHweoEVtURR7IKYIL7VbDBt6ol-CpfD06_9UbQ8hCHSaZ7Mo8L62IjCyQqRjU2FzdGnUMJgt6fGKat5pbJEOMkT7YRz3lUqF6hjmSVaJS55Blt1U7sXwKTFn4f3VYxeMQIDX3HBDbc2kzyLvdQ9OEAtlctJNCvb-LhA_6TryB687xRYmiWFOZ2kcX2X6OFKdBJ4O-4UwlGwuk9M26OTTyWVEW0PXvkv3oM33SApUVkUT9G1axbYPiUleo-ZUOtlRGDYQRjYg-dhhK3eJ2QiJHo4L-_77lfwEHFam0nPxT5szacL9xqx0Lw6aOfCb-lAA6E
linkProvider American Chemical Society
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwELZoOZQLlGcX2mIQBy4psRM7yXG1ZbWFbVVBK_UWOX5ooSVZbXY5cOKnd8ZOlodaQY6O40zscfzN2PMNIW-ywtgs0zqyUuoodXEeKV6IKHesKIw2THtnzvGJnJynHy7ERUeTg7EwIEQLLbV-E_8XuwB793UOyAVsEbdB7gqZSkzTMBx9XhtXgvusjrAcoTkUy55F6PdHcQXS7R8r0MYMzz_eBi79IjN-ELIVefH82ZLLg9WyOtA__mJu_D_5t8n9DmvSYVCOh-SOrR-RrVGf4u0x-fkJYGKEUSA0zG108tHGUaTM_dbMZ83C0qO2wV2dEK5JVW3ooUV2hyb4EWkIdKQAJOnpDIoxUiL4ebElLB5fraAhTxtFT5EX4ktNDxdNPVdPyPn4_dloEnUpGSKV5skyKoyLNS-sqADnmJSbHCwMyTX0fqqtNIpVMku4FSxRllvrbCVzDiMuskTJxCZPyWbd1HaHUGHgV-JcFYONDDDBVYwzzYzJBMtiJ9SA7EM_lt2Uaku_W87BWuk7ckDe9uNY6o7QHPNqXN1U9fW66jyweNxYCZRhfR95tyfDaYllSOIDV_6dDcirXldKGCzcXVG1bVYgnxQCbMmMy9vr8MC3A6BwQJ4FRVu_j4uEC7B3nv_ru1-SrcnZ8bScHp18fEHuAYLzMfaM75LN5WJl9wAlLat9Pz2uAVW_DAM
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwELZokaCX8m6XRzGIA5eU2Imd5LjaZbWFUlZApd4ixw9tS0mizS4HTvx0ZpyHALWCHB3HsWM7_r6x5xtCXiWZsUmidWCl1EHswjRQPBNB6liWGW2Y9sacDydyfhq_OxNnHVFEXxioRAMlNX4TH2d1bVynMMDeXNSAXoCPuC1yE4AIw1AN48nngWAJ7iM7wpKElCiUvZLQ74_iKqSbP1ahrSWegbwOYPqFZnaHfByq6M-XfD3crItD_eMv9cb_b8NdstthTjpuB8k9csOW98ntSR_q7QH5-QngYoDeILSd42jso5WjKJ37raqX1crSo6bC3Z3WbZOq0tCpRZWHqrUn0tbhkQKgpIslJKPHRGvvxZIweXa5gYK8fBRdoD7EeUmnq6qs1UNyOnv7ZTIPutAMgYrTaB1kxoWaZ1YUgHdMzE0KTENyDT0QayuNYoVMIm4Fi5Tl1jpbyJRDz4skUjKy0SOyXVal3SdUGPilOFeEwJUBLriCcaaZMYlgSeiEGpED-JZ5N7Wa3O-ac2At_Ycckdd9X-a6EzbH-BqXV2V9OWStWzWPKzPBgBjuo_72fHycYxqK-cCVfmcj8qIfLzl0Fu6yqNJWG6ifFAI4ZcLl9Xl4q7sD4HBE9trBNryPi4gL4D2P_9Xu5-TWYjrLj49O3j8hOwDkvKs940_J9nq1sc8ALK2LAz9DfgHlGQ59
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Real-time+monitoring+of+chromophore+isomerization+and+deprotonation+during+the+photoactivation+of+the+fluorescent+protein+Dronpa&rft.jtitle=The+journal+of+physical+chemistry.+B&rft.au=Yadav%2C+Dheerendra&rft.au=Lacombat%2C+Fabien&rft.au=Dozova%2C+Nadia&rft.au=Rappaport%2C+Fabrice&rft.date=2015-02-12&rft.eissn=1520-5207&rft.volume=119&rft.issue=6&rft.spage=2404&rft_id=info:doi/10.1021%2Fjp507094f&rft_id=info%3Apmid%2F25325882&rft.externalDocID=25325882
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1520-6106&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1520-6106&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1520-6106&client=summon