Evidence map›Paper›PMID 34472331›Full record

ArticleACS nano2021

Subcellular Targeted Nanohoop for One- and Two-Photon Live Cell Imaging.

Terri C Lovell, Sarah G Bolton, John P Kenison, Julia Shangguan, Claire E Otteson, Fehmi Civitci, Xiaolin Nan, Michael D Pluth, Ramesh Jasti

Abstract read
In one paragraph

Article in ACS nano, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Bridging [8]cyclo-Chemical science · 2026
    Article
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  8. Article
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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

9 authors.

Terri C LovellDepartment of Chemistry & Biochemistry, Materials Science Institute, Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, Oregon 97403, United States.ORCID 0000-0003-1722-584X
Sarah G BoltonDepartment of Chemistry & Biochemistry, Materials Science Institute, Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, Oregon 97403, United States.
John P KenisonKnight Cancer Early Detection Advanced Research Center, Oregon Health and Science University, 2720 S. Moody Avenue, Portland, Oregon 97201, United States.
Julia ShangguanDepartment of Biomedical Engineering, Oregon Health and Science University, 2730 S. Moody Avenue, Portland, Oregon 97201, United States.
Claire E OttesonDepartment of Chemistry & Biochemistry, Materials Science Institute, Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, Oregon 97403, United States.ORCID 0000-0002-0095-6729
Fehmi CivitciKnight Cancer Early Detection Advanced Research Center, Oregon Health and Science University, 2720 S. Moody Avenue, Portland, Oregon 97201, United States.
Xiaolin NanKnight Cancer Early Detection Advanced Research Center, Oregon Health and Science University, 2720 S. Moody Avenue, Portland, Oregon 97201, United States.ORCID 0000-0002-0597-0255
Michael D PluthDepartment of Chemistry & Biochemistry, Materials Science Institute, Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, Oregon 97403, United States.ORCID 0000-0003-3604-653X
Ramesh JastiDepartment of Chemistry & Biochemistry, Materials Science Institute, Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, Oregon 97403, United States.ORCID 0000-0002-8606-6339

Funding

MOLECULAR BIOLOGY AND BIOPHYSICST32GM007759 · NIGMS · UNIVERSITY OF OREGON · PI NOLEN, BRADLEY J · 1985 to 2021
$8.5M
Supplement to: Chemical Tools for Delivery and Detection of Biological Hydrogen SulfideR01GM113030 · NIGMS · UNIVERSITY OF OREGON · PI PLUTH, MICHAEL · 2015 to 2024
$2.8M
Defining mechanisms of Ras clustering and signaling in membrane nanodomains with multiplexed superresolution and correlative microscopiesR01GM132322 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI NAN, XIAOLIN · 2020 to 2023
$1.4M
NIGMS NIH HHS R01 GM113030NIGMS NIH HHS R01 GM132322NIGMS NIH HHS T32 GM007759
6 · The paper itself

Abstract

Fluorophores are powerful tools for interrogating biological systems. Carbon nanotubes (CNTs) have long been attractive materials for biological imaging due to their near-infrared excitation and bright, tunable optical properties. The difficulty in synthesizing and functionalizing these materials with precision, however, has hampered progress in this area. Carbon nanohoops, which are macrocyclic CNT substructures, are carbon nanostructures that possess ideal photophysical characteristics of nanomaterials, while maintaining the precise synthesis of small molecules. However, much work remains to advance the nanohoop class of fluorophores as biological imaging agents. Herein, we report an intracellular targeted nanohoop. This fluorescent nanostructure is noncytotoxic at concentrations up to 50 μM, and cellular uptake investigations indicate internalization through endocytic pathways. Additionally, we employ this nanohoop for two-photon fluorescence imaging, demonstrating a high two-photon absorption cross-section (65 GM) and photostability comparable to a commercial probe. This work further motivates continued investigations into carbon nanohoop photophysics and their biological imaging applications.

Indexed as

Nanotubes, CarbonNanotubes, Carbonaromatic moleculescell imagingcycloparaphenylenefluorophorenanohoop

Identifiers

PMID34472331
PMCPMC8764753

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Registered trials

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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.