Title
Rapid fabrication of precise high-throughput filters from membrane protein nanosheets
Date Issued
01 March 2020
Access level
metadata only access
Resource Type
journal article
Author(s)
Tu Y.M.
Song W.
Ren T.
Shen Y.x.
Chowdhury R.
Rajapaksha P.
Culp T.E.
Samineni L.
Lang C.
Thokkadam A.
Carson D.
Dai Y.
Mukthar A.
Zhang M.
Parshin A.
Sloand J.N.
Medina S.H.
Grzelakowski M.
Bhattacharya D.
Phillip W.A.
Hickey R.J.
Wei Y.
Kumar M.
Pennsylvania State University
Publisher(s)
Nature Research
Abstract
Biological membranes are ideal for separations as they provide high permeability while maintaining high solute selectivity due to the presence of specialized membrane protein (MP) channels. However, successful integration of MPs into manufactured membranes has remained a significant challenge. Here, we demonstrate a two-hour organic solvent method to develop 2D crystals and nanosheets of highly packed pore-forming MPs in block copolymers (BCPs). We then integrate these hybrid materials into scalable MP-BCP biomimetic membranes. These MP-BCP nanosheet membranes maintain the molecular selectivity of the three types of β-barrel MP channels used, with pore sizes of 0.8 nm, 1.3 nm, and 1.5 nm. These biomimetic membranes demonstrate water permeability that is 20–1,000 times greater than that of commercial membranes and 1.5–45 times greater than that of the latest research membranes with comparable molecular exclusion ratings. This approach could provide high performance alternatives in the challenging sub-nanometre to few-nanometre size range.
Start page
347
End page
354
Volume
19
Issue
3
Language
English
OCDE Knowledge area
Ingeniería de materiales
Bioquímica, Biología molecular
Scopus EID
2-s2.0-85078494100
PubMed ID
Source
Nature Materials
ISSN of the container
14761122
Sponsor(s)
The authors acknowledge financial support from the National Science Foundation (NSF) CAREER grant (CBET-1552571), NSF grant CBET-1709522 and NSF grant CBET-1804836 to M.K. for this work. T.C. and E.D.G. acknowledge financial support from NSF DMR-1609417. The authors also thank M. Hazen and J. Cantolina for their help with cross-sectional sample preparation. We thank L. Movileanu for the kind gift of the plasmid for expressing the FhuA ΔC/Δ4L protein.
Sources of information:
Directorio de Producción Científica
Scopus