Evidence map›Paper›PMID 39997105›Full record

ArticleBiomimetics (Basel, Switzerland)2025

Design and Development of Natural-Product-Derived Nanoassemblies and Their Interactions with Alpha Synuclein.

Ipsita A Banerjee, Amrita Das, Mary A Biggs, Chau Anh N Phan, Liana R Cutter, Alexandra R Ren

Abstract read
In one paragraph

Article in Biomimetics (Basel, Switzerland), 2025. 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

6 authors.

Ipsita A BanerjeeDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, NY 10458, USA.ORCID 0000-0002-6987-9717
Amrita DasDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, NY 10458, USA.
Mary A BiggsDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, NY 10458, USA.ORCID 0000-0002-1224-8578
Chau Anh N PhanDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, NY 10458, USA.
Liana R CutterDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, NY 10458, USA.
Alexandra R RenDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, NY 10458, USA.

Funding

Blavatnik Family Foundation NAFordham University NAHenry Luce Foundation NANSF NSF-MRI Grant # (2117625)
6 · The paper itself

Abstract

Biomimetic nanoassemblies derived from natural products are considered promising nanomaterials due to their self-assembling ability and their favorable interactions with biological molecules leading to their numerous applications as therapeutic agents or as molecular probes. In this work, we have created peptide nanoconjugates of two natural products, β-Boswellic acid (BA) and β-glycyrrhetinic acid (GH). Both BA and GH are known for their medicinal value, including their role as strong antioxidants, anti-inflammatory, neuroprotective and as anti-tumor agents. To enhance the bioavailability of these molecules, they were functionalized with three short peptides (YYIVS, MPDAHL and GSGGL) to create six conjugates with amphiphilic structures capable of facile self-assembly. The peptides were also derived from natural sources and have been known to display antioxidant activity. Depending upon the conjugate, nanofibers, nanovesicles or a mixture of both were formed upon self-assembly. The binding interactions of the nanoconjugates with α-Synuclein, a protein implicated in Parkinson's disease (PD) was examined through in silico studies and FTIR, circular dichroism and imaging studies. Our results indicated that the nanoassemblies interacted with alpha-synuclein fibrils efficaciously. Furthermore, the nanoassemblies were found to demonstrate high viability in the presence of microglial cells, and were found to enhance the uptake and interactions of α-Synuclein with microglial cells. The nanoconjugates designed in this work may be potentially utilized as vectors for peptide-based drug delivery or for other therapeutic applications.

Indexed as

alpha synucleincellular uptakenanoassembliesself-assemblyterpenes

Identifiers

PMID39997105
PMCPMC11852371

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.