Evidence map›Paper›PMID 34907186›Full record

ArticleNature communications2021

Tracking excited state decay mechanisms of pyrimidine nucleosides in real time.

Rocío Borrego-Varillas, Artur Nenov, Piotr Kabaciński, Irene Conti, Lucia Ganzer, Aurelio Oriana, Vishal Kumar Jaiswal, Ines Delfino, Oliver Weingart, Cristian Manzoni and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
8.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 74 citations in OpenAlex.

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  9. The OpenMolcasJournal of chemical theory and computation · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 3 countries.

Rocío Borrego-Varillas *IFN-CNR, Piazza Leonardo da Vinci 32, Milano, Italy.ORCID http://orcid.org/0000-0002-4499-0558
Artur Nenov *Dipartimento di Chimica Industriale, Università degli Studi di Bologna, Viale del Risorgimento 4, Bologna, Italy.ORCID http://orcid.org/0000-0003-3071-5341
Piotr KabacińskiDipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, Italy.ORCID http://orcid.org/0000-0003-4591-5100
Irene ContiDipartimento di Chimica Industriale, Università degli Studi di Bologna, Viale del Risorgimento 4, Bologna, Italy.
Lucia GanzerDipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, Italy.
Aurelio OrianaDipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, Italy.
Vishal Kumar JaiswalDipartimento di Chimica Industriale, Università degli Studi di Bologna, Viale del Risorgimento 4, Bologna, Italy.ORCID http://orcid.org/0000-0002-5090-7984
Ines DelfinoDipartimento di Scienze Ecologiche e Biologiche, Università della Tuscia, Via San Camillo de Lellis, snc, Viterbo, Italy.
Oliver WeingartInstitut für Theoretische Chemie und Computerchemie, Heinrich Heine Universität Düsseldorf, Universitätsstrasse 1, Düsseldorf, Germany.
Cristian ManzoniIFN-CNR, Piazza Leonardo da Vinci 32, Milano, Italy.ORCID http://orcid.org/0000-0002-4169-8869
Ivan RivaltaDipartimento di Chimica Industriale, Università degli Studi di Bologna, Viale del Risorgimento 4, Bologna, Italy.ORCID http://orcid.org/0000-0002-1208-602X
Marco GaravelliDipartimento di Chimica Industriale, Università degli Studi di Bologna, Viale del Risorgimento 4, Bologna, Italy. marco.garavelli@unibo.it.ORCID http://orcid.org/0000-0002-0796-289X
Giulio CerulloIFN-CNR, Piazza Leonardo da Vinci 32, Milano, Italy. giulio.cerullo@polimi.it.ORCID http://orcid.org/0000-0002-9534-2702
Politecnico di Milano · ITUniversity of Bologna · ITIstituto di Fotonica e Nanotecnologie · ITHeinrich Heine University Düsseldorf · DEUniversità degli Studi della Tuscia · ITUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA owes its remarkable photostability to its building blocks-the nucleosides-that efficiently dissipate the energy acquired upon ultraviolet light absorption. The mechanism occurring on a sub-picosecond time scale has been a matter of intense debate. Here we combine sub-30-fs transient absorption spectroscopy experiments with broad spectral coverage and state-of-the-art mixed quantum-classical dynamics with spectral signal simulations to resolve the early steps of the deactivation mechanisms of uridine (Urd) and 5-methyluridine (5mUrd) in aqueous solution. We track the wave packet motion from the Franck-Condon region to the conical intersections (CIs) with the ground state and observe spectral signatures of excited-state vibrational modes. 5mUrd exhibits an order of magnitude longer lifetime with respect to Urd due to the solvent reorganization needed to facilitate bulky methyl group motions leading to the CI. This activates potentially lesion-inducing dynamics such as ring opening. Involvement of the

Indexed as

Photochemical ProcessesPyrimidine NucleosidesPyrimidinesSolventsSpectrophotometry, UltravioletUltraviolet RaysUridineVibrationPyrimidine NucleosidesPyrimidinesribothymidineSolventsUridine

Identifiers

PMID34907186
PMCPMC8671501
OpenAlexW4226007238

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.