Evidence map›Paper›PMID 39189351›Full record

ArticleACS nano2024

Assembly of Differently Sized Supercharged Protein Nanocages into Superlattices for Construction of Binary Nanoparticle-Protein Materials.

Michael Rütten, Laurin Lang, Henrike Wagler, Marcel Lach, Niklas Mucke, Ulrike Laugks, Carolin Seuring, Thomas F Keller, Andreas Stierle, Helen M Ginn and 1 more

Abstract read
In one paragraph

Article in ACS nano, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Protein Cage Directed Assembly of Binary Nanoparticle Superlattices.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

11 authors.

Michael RüttenInstitute of Physical Chemistry, Department of Chemistry, University of Hamburg, Hamburg 20146, Germany.
Laurin LangInstitute of Physical Chemistry, Department of Chemistry, University of Hamburg, Hamburg 20146, Germany.
Henrike WaglerInstitute of Physical Chemistry, Department of Chemistry, University of Hamburg, Hamburg 20146, Germany.
Marcel LachInstitute of Physical Chemistry, Department of Chemistry, University of Hamburg, Hamburg 20146, Germany.
Niklas MuckeInstitute of Physical Chemistry, Department of Chemistry, University of Hamburg, Hamburg 20146, Germany.
Ulrike LaugksCentre for Structureal Systems Biology (CSSB), Hamburg 22607, Germany.
Carolin SeuringThe Hamburg Centre for Ultrafast Imaging, University of Hamburg, Hamburg 20146, Germany.
Thomas F KellerCentre for X-ray and Nano Science (CXNS), Deutsches Elektronen-Synchrotron DESY, Hamburg 22607, Germany.ORCID 0000-0002-3770-6344
Andreas StierleCentre for X-ray and Nano Science (CXNS), Deutsches Elektronen-Synchrotron DESY, Hamburg 22607, Germany.ORCID 0000-0002-0303-6282
Helen M GinnCenter for Free-Electron Laser Science (CFEL), Deutsches Elektronen-Synchrotron DESY, Hamburg 22607, Germany.
Tobias BeckInstitute of Physical Chemistry, Department of Chemistry, University of Hamburg, Hamburg 20146, Germany.ORCID 0000-0001-7398-3982

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study focuses on the design and characterization of binary nanoparticle superlattices: Two differently sized, supercharged protein nanocages are used to create a matrix for nanoparticle arrangement. We have previously established the assembly of protein nanocages of the same size. Here, we present another approach for multicomponent biohybrid material synthesis by successfully assembling two differently sized supercharged protein nanocages with different symmetries. Typically, the ordered assembly of objects with nonmatching symmetry is challenging, but our electrostatic-based approach overcomes the symmetry mismatch by exploiting electrostatic interactions between oppositely charged cages. Moreover, our study showcases the use of nanoparticles as a contrast enhancer in an elegant way to gain insights into the structural details of crystalline biohybrid materials. The assembled materials were characterized with various methods, including transmission electron microscopy (TEM) and single-crystal small-angle X-ray diffraction (SC-SAXD). We employed cryo-plasma-focused ion beam milling (cryo-PFIB) to prepare lamellae for the investigation of nanoparticle sublattices via electron cryo-tomography. Importantly, we refined superlattice structure data obtained from single-crystal SAXD experiments, providing conclusive evidence of the final assembly type. Our findings highlight the versatility of protein nanocages for creating distinctive types of binary superlattices. Because the nanoparticles do not influence the type of assembly, protein cage matrices can combine various nanoparticles in the solid state. This study not only contributes to the expanding repertoire of nanoparticle assembly methods but also demonstrates the power of advanced characterization techniques in elucidating the structural intricacies of these biohybrid materials.

Indexed as

Particle SizeNanoparticlesProteinsProteinsbinary superlatticesbiohybrid nanomaterialselectrostatic assemblyinorganic nanoparticlesprotein cagesSAXSsingle-crystal small-angle X-ray diffraction SC-SAXD

Identifiers

PMID39189351
PMCPMC11394343

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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.