Evidence map›Paper›PMID 33681146›Full record

ArticleFrontiers in chemistry2021

Spectroscopic and Photophysical Investigation of Model Dipyrroles Common to Bilins: Exploring Natural Design for Steering Torsion to Divergent Functions.

Clayton F Staheli, Jaxon Barney, Taime R Clark, Maxwell Bowles, Bridger Jeppesen, Daniel G Oblinsky, Mackay B Steffensen, Jacob C Dean

Open access · goldAbstract read
In one paragraph

Article in Frontiers in chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Complex Multistate Photophysics of a Rhodanine Photoswitch.Angewandte Chemie (International ed. in English) · 2025
    Article
  2. Article
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

8 authors at 3 institutions in 1 country.

Clayton F StaheliDepartment of Physical Science, Southern Utah University, Cedar City, UT, United States.
Jaxon BarneyDepartment of Physical Science, Southern Utah University, Cedar City, UT, United States.
Taime R ClarkDepartment of Physical Science, Southern Utah University, Cedar City, UT, United States.
Maxwell BowlesDepartment of Physical Science, Southern Utah University, Cedar City, UT, United States.
Bridger JeppesenDepartment of Physical Science, Southern Utah University, Cedar City, UT, United States.
Daniel G OblinskyDepartment of Chemistry, Princeton University, Princeton, NJ, United States.
Mackay B SteffensenDepartment of Physical Science, Southern Utah University, Cedar City, UT, United States.
Jacob C DeanDepartment of Physical Science, Southern Utah University, Cedar City, UT, United States.
Southern Utah University · USPennsylvania State University · USPrinceton University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biliproteins are a unique class of photosynthetic proteins in their diverse, and at times, divergent biophysical function. The two contexts of photosynthetic light harvesting and photoreception demonstrate characteristically opposite criteria for success, with light harvesting demanding structurally-rigid chromophores which minimize excitation quenching, and photoreception requiring structural flexibility to enable conformational isomerization. The functional plasticity borne out in these two biological contexts is a consequence of the structural plasticity of the pigments utilized by biliproteins-linear tetrapyrroles, or bilins. In this work, the intrinsic flexibility of the bilin framework is investigated in a bottom-up fashion by reducing the active nuclear degrees of freedom through model dipyrrole subunits of the bilin core and terminus free of external protein interactions. Steady-state spectroscopy was carried out on the dipyrrole (DPY) and dipyrrinone (DPN) subunits free in solution to characterize their intrinsic spectroscopic properties including absorption strengths and nonradiative activity. Transient absorption (TA) spectroscopy was utilized to determine the mechanism and kinetics of nonradiative decay of the dipyrrole subunits, revealing dynamics dominated by rapid internal conversion with some

Indexed as

BilinsDipyrroleslight harvestingphotoreceptionPhycobiliproteinstorsional deactivationZ-E isomerization

Identifiers

PMID33681146
PMCPMC7925881
OpenAlexW3132698449

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.