Identification of Microorganisms that Bind Specifically to Target Materials of Interest Using a Magnetophoretic Microfluidic Platform.

bacterial surface display library environmental microorganism screening magnetic separation material-binding microorganism and peptide microfluidic screening platform

Journal

ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991

Informations de publication

Date de publication:
08 Mar 2023
Historique:
pubmed: 28 2 2023
medline: 11 3 2023
entrez: 27 2 2023
Statut: ppublish

Résumé

Discovery of microorganisms and their relevant surface peptides that specifically bind to target materials of interest can be achieved through iterative biopanning-based screening of cellular libraries having high diversity. Recently, microfluidics-based biopanning methods have been developed and exploited to overcome the limitations of conventional methods where controlling the shear stress applied to remove cells that do not bind or only weakly bind to target surfaces is difficult and the overall experimental procedure is labor-intensive. Despite the advantages of such microfluidic methods and successful demonstration of their utility, these methods still require several rounds of iterative biopanning. In this work, a magnetophoretic microfluidic biopanning platform was developed to isolate microorganisms that bind to target materials of interest, which is gold in this case. To achieve this, gold-coated magnetic nanobeads, which only attached to microorganisms that exhibit high affinity to gold, were used. The platform was first utilized to screen a bacterial peptide display library, where only the cells with surface peptides that specifically bind to gold could be isolated by the high-gradient magnetic field generated within the microchannel, resulting in enrichment and isolation of many isolates with high affinity and high specificity toward gold even after only a single round of separation. The amino acid profile of the resulting isolates was analyzed to provide a better understanding of the distinctive attributes of peptides that contribute to their specific material-binding capabilities. Next, the microfluidic system was utilized to screen soil microbes, a rich source of extremely diverse microorganisms, successfully isolating many naturally occurring microorganisms that show strong and specific binding to gold. The results show that the developed microfluidic platform is a powerful screening tool for identifying microorganisms that specifically bind to a target material surface of interest, which can greatly accelerate the development of new peptide-driven biological materials and hybrid organic-inorganic materials.

Identifiants

pubmed: 36847552
doi: 10.1021/acsami.2c15192
doi:

Substances chimiques

Peptide Library 0
Peptides 0
Gold 7440-57-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11391-11402

Auteurs

Song-I Han (SI)

Department of Electrical and Computer Engineering, Texas A&M University, College Station, Texas 77843, USA.

Deborah A Sarkes (DA)

Biotechnology Branch, U.S. Army Combat Capabilities Development Command (DEVCOM), Army Research Laboratory (ARL), Adelphi, Maryland 20783, USA.

Margaret M Hurley (MM)

Biotechnology Branch, U.S. Army Combat Capabilities Development Command (DEVCOM), Army Research Laboratory (ARL), Adelphi, Maryland 20783, USA.

Rebecca Renberg (R)

Biotechnology Branch, U.S. Army Combat Capabilities Development Command (DEVCOM), Army Research Laboratory (ARL), Adelphi, Maryland 20783, USA.

Can Huang (C)

Department of Electrical and Computer Engineering, Texas A&M University, College Station, Texas 77843, USA.

Yuwen Li (Y)

Department of Electrical and Computer Engineering, Texas A&M University, College Station, Texas 77843, USA.

Justin P Jahnke (JP)

Biotechnology Branch, U.S. Army Combat Capabilities Development Command (DEVCOM), Army Research Laboratory (ARL), Adelphi, Maryland 20783, USA.

James J Sumner (JJ)

Biotechnology Branch, U.S. Army Combat Capabilities Development Command (DEVCOM), Army Research Laboratory (ARL), Adelphi, Maryland 20783, USA.

Dimitra N Stratis-Cullum (DN)

Biotechnology Branch, U.S. Army Combat Capabilities Development Command (DEVCOM), Army Research Laboratory (ARL), Adelphi, Maryland 20783, USA.

Arum Han (A)

Department of Electrical and Computer Engineering, Texas A&M University, College Station, Texas 77843, USA.
Department of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, USA.
Department of Chemical Engineering, Texas A&M University, College Station, Texas 77843, USA.

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Classifications MeSH