Evidence map›Paper›PMID 39474933›Full record

ArticleACS applied materials & interfaces2024

Facile Mechanochemical Functionalization of Hydrophobic Substrates for Single-Walled Carbon Nanotube Based Optical Reporters of Hydrolase Activity.

Abbas Elhambakhsh, Mohaddeseh Abbasi, Cole R Dutter, Marshall D McDaniel, Brett VanVeller, Andrew C Hillier, Nigel F Reuel

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Abbas ElhambakhshDepartment of Chemical and Biological Engineering, Iowa State University, 618 Bissell Rd., Ames, Iowa 50011, United States.
Mohaddeseh AbbasiDepartment of Chemistry, Iowa State University, Ames, Iowa 50011, United States.
Cole R DutterDepartment of Agronomy, Iowa State University, Ames, Iowa 50011, United States.ORCID 0000-0002-8098-7639
Marshall D McDanielDepartment of Agronomy, Iowa State University, Ames, Iowa 50011, United States.
Brett VanVellerDepartment of Chemistry, Iowa State University, Ames, Iowa 50011, United States.ORCID 0000-0002-3792-0308
Andrew C HillierDepartment of Chemical and Biological Engineering, Iowa State University, 618 Bissell Rd., Ames, Iowa 50011, United States.ORCID 0000-0002-2729-1368
Nigel F ReuelDepartment of Chemical and Biological Engineering, Iowa State University, 618 Bissell Rd., Ames, Iowa 50011, United States.ORCID 0000-0003-3438-2919

Funding

Unsupervised optimization of protein therapeutics using closed-loop in vitro synthesis, nanosensing,and deep-learningR35GM138265 · NIGMS · IOWA STATE UNIVERSITY · PI Nigel F Reuel · 2020 to 2026
$2.3M
NIGMS NIH HHS R35 GM138265
6 · The paper itself

Abstract

Single walled carbon nanotubes (SWCNT) have recently been demonstrated as modular, near-infrared (nIR) probes for reporting hydrolase activity; however, these have been limited to naturally amphipathic substrate targets used to noncovalently functionalize the hydrophobic nanoparticles. Many relevant substrate targets are hydrophobic (such as recalcitrant biomass) and pose a challenge for modular functionalization. In this work, a facile mechanochemistry approach was used to couple insoluble substrates, such as lignin, to SWCNT using l-lysine amino acid as a linker and tip sonication as the mechanochemical energy source. The proposed coupling mechanism is ion pairing between the lysine amines and lignin carboxylic acids, as evidenced by FTIR, NMR, SEM, and elemental analyses. The limits of detection for the lignin-lysine-SWCNT (LLS) probe were established using commercial enzymes and found to be 0.25 ppm (volume basis) of the formulated product. Real-world use of the LLS probes was shown by evaluating soil hydrolase activities of soil samples gathered from different corn root proximal locations and soil types. Additionally, the probes were used to determine the effect of storage temperature on the measured enzyme response. The modularity of this mechanochemical functionalization approach is demonstrated with other substrates such as zein and 9-anthracenecarboxylic acid, which further corroborate the mechanochemical mechanism.

Indexed as

HydrolasesHydrophobic and Hydrophilic InteractionsNanotubes, CarbonCarboxylic AcidsLigninLysineCarboxylic AcidsHydrolasesLigninLysineNanotubes, Carbonactivity measurementcarbon nanotubeshydrolaseligninmechanochemistrysoil enzymes

Identifiers

PMID39474933
PMCPMC11730026

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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.