ArticleJournal of the American Chemical Society2017
Protein-Mediated Colloidal Assembly.
Article in Journal of the American Chemical Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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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.
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.
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Who cites it
11 citing papers in PubMed.
- Cohesive Living Bacterial Films with Tunable Mechanical Properties from Cell Surface Protein Display.ACS synthetic biology · 2024Article
- Self assembling nanoparticle enzyme clusters provide access to substrate channeling in multienzymatic cascades.Nature communications · 2023Article
- Article
- BScience advances · 2022Article
- Genetically Programmable Microbial Assembly.ACS synthetic biology · 2021Article
- Injectable, photoresponsive hydrogels for delivering neuroprotective proteins enabled by metal-directed protein assembly.Science advances · 2020Article
- Orthogonal Blue and Red Light Controlled Cell-Cell Adhesions Enable Sorting-out in Multicellular Structures.ACS synthetic biology · 2020Article
- Interplay between Short-Range Attraction and Long-Range Repulsion Controls Reentrant Liquid Condensation of Ribonucleoprotein-RNA Complexes.Journal of the American Chemical Society · 2019Article
- Colloidal stability versus self-assembly of nanoparticles controlled by coiled-coil protein interactions.Soft matter · 2019Article
- Peptide-induced super-assembly of biocatalytic metal-organic frameworks for programmed enzyme cascades.Chemical science · 2019Article
- Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Programmable colloidal assembly enables the creation of mesoscale materials in a bottom-up manner. Although DNA oligonucleotides have been used extensively as the programmable units in this paradigm, proteins, which exhibit more diverse modes of association and function, have not been widely used to direct colloidal assembly. Here we use protein-protein interactions to drive controlled aggregation of polystyrene microparticles, either through reversible coiled-coil interactions or through intermolecular isopeptide linkages. The sizes of the resulting aggregates are tunable and can be controlled by the concentration of immobilized surface proteins. Moreover, particles coated with different protein pairs undergo orthogonal assembly. We demonstrate that aggregates formed by association of coiled-coil proteins, in contrast to those linked by isopeptide bonds, are dispersed by treatment with chemical denaturants or soluble competing proteins. Finally, we show that protein-protein interactions can be used to assemble complex core-shell aggregates. This work illustrates a versatile strategy for engineering colloidal systems for use in materials science and biotechnology.
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Registered trials
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.