Evidence map›Paper›PMID 38412617›Full record

ArticleACS nano2024

Nanopatterned Monolayers of Bioinspired, Sequence-Defined Polypeptoid Brushes for Semiconductor/Bio Interfaces.

Beihang Yu, Boyce S Chang, Whitney S Loo, Scott Dhuey, Padraic O'Reilly, Paul D Ashby, Michael D Connolly, Grigory Tikhomirov, Ronald N Zuckermann, Ricardo Ruiz

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Sequence-defined peptoidsChemical science · 2025
    Article
  6. Review
  7. Review
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

10 authors.

Beihang YuThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0001-5060-0766
Boyce S ChangThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0001-8683-3369
Whitney S LooThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0002-9773-3571
Scott DhueyThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0002-9185-2510
Padraic O'ReillyMolecular Vista Inc., San Jose, California 95119, United States.
Paul D AshbyThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0003-4195-310X
Michael D ConnollyThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Grigory TikhomirovDepartment of Electrical Engineering and Computer Sciences, University of California, Berkeley, Berkeley, California 94709, United States.ORCID 0000-0001-6061-3843
Ronald N ZuckermannThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0002-3055-8860
Ricardo RuizThe Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0002-1698-4281

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to control and manipulate semiconductor/bio interfaces is essential to enable biological nanofabrication pathways and bioelectronic devices. Traditional surface functionalization methods, such as self-assembled monolayers (SAMs), provide limited customization for these interfaces. Polymer brushes offer a wider range of chemistries, but choices that maintain compatibility with both lithographic patterning and biological systems are scarce. Here, we developed a class of bioinspired, sequence-defined polymers, i.e., polypeptoids, as tailored polymer brushes for surface modification of semiconductor substrates. Polypeptoids featuring a terminal hydroxyl (-OH) group are designed and synthesized for efficient melt grafting onto the native oxide layer of Si substrates, forming ultrathin (∼1 nm) monolayers. By programming monomer chemistry, our polypeptoid brush platform offers versatile surface modification, including adjustments to surface energy, passivation, preferential biomolecule attachment, and specific biomolecule binding. Importantly, the polypeptoid brush monolayers remain compatible with electron-beam lithographic patterning and retain their chemical characteristics even under harsh lithographic conditions. Electron-beam lithography is used over polypeptoid brushes to generate highly precise, binary nanoscale patterns with localized functionality for the selective immobilization (or passivation) of biomacromolecules, such as DNA origami or streptavidin, onto addressable arrays. This surface modification strategy with bioinspired, sequence-defined polypeptoid brushes enables monomer-level control over surface properties with a large parameter space of monomer chemistry and sequence and therefore is a highly versatile platform to precisely engineer semiconductor/bio interfaces for bioelectronics applications.

Indexed as

PolymersAdsorptionSurface PropertiesPolymersnanopatterned polymer brushesselective immobilization of biomoleculessemiconductor/bio interfacessequence-defined polymerssurface modification

Identifiers

PMID38412617
PMCPMC10938923

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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.