Evidence map›Paper›PMID 42461544›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Nanoporous Gold for Enzyme Immobilization.

Keith J Stine, Kenise Jefferson, Olga V Shulga, Palak Sondhi, Dhanbir Lingden

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

5 authors.

Keith J StineDepartment of Chemistry and Biochemistry, One University Boulevard, University of Missouri-Saint Louis, Saint Louis, MO, 63121-4400, USA. kstine@umsl.edu.
Kenise JeffersonDepartment of Chemistry and Biochemistry, One University Boulevard, University of Missouri-Saint Louis, Saint Louis, MO, 63121-4400, USA.
Olga V ShulgaDepartment of Chemistry and Biochemistry, One University Boulevard, University of Missouri-Saint Louis, Saint Louis, MO, 63121-4400, USA.
Palak SondhiDepartment of Chemistry and Biochemistry, One University Boulevard, University of Missouri-Saint Louis, Saint Louis, MO, 63121-4400, USA.
Dhanbir LingdenDepartment of Chemistry and Biochemistry, One University Boulevard, University of Missouri-Saint Louis, Saint Louis, MO, 63121-4400, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoporous gold (NPG) is a material of emerging interest for the immobilization of biomolecules and especially enzymes. The material provides a high surface area form of gold that is suitable for physisorption or covalent modification by self-assembled monolayers. The material can be used as a high surface area electrode and with immobilized enzymes can be used for the development of amperometric biosensors. NPG can be prepared in a variety of formats from alloys containing between 20% and 50% atomic composition of gold and less noble element(s) by dealloying procedures. NPG can be prepared in a variety of shapes (e.g., wire, rod, sphere, plate, and supported film) and dimensions (e.g., 0-3D). Colloidal 0D NPG nanoparticles possess a higher surface area-to-volume ratio and enhanced optical properties. Materials resembling NPG can be prepared by hydrothermal and electrodeposition methods. Related high surface area gold structures have been prepared using templating approaches. Hierarchical bimodal nanoporous gold (hb-NPG) structures containing both macropores and mesopores have been engineered. NPG with a bimodal porous structure has the advantage of a large specific surface area for functionalization combined with rapid transport pathways for molecules into and out of the structure. Materials with porous architectures are potential candidates for achieving covalent enzyme immobilization by first forming a self-assembled monolayer bearing a terminal reactive functional group followed by conjugation to the enzyme through amide linkages to lysine residues. Enzymes can also be entrapped by physisorption or immobilized by electrostatic interactions.

Indexed as

Enzymes, ImmobilizedGoldMetal NanoparticlesNanoporesBiosensing TechniquesElectrodesPorositySurface PropertiesEnzymes, ImmobilizedGoldBioconjugationEnzyme immobilizationHierarchical bimodal goldNanoporous goldNanoporous gold nanoparticlesSelf-assembled monolayer

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.