Scalable biomimetic sensing system with membrane receptor dual-monolayer probe and graphene transistor arrays

Author:

Qing Rui123ORCID,Xue Mantian4ORCID,Zhao Jiayuan5,Wu Lidong6ORCID,Breitwieser Andreas7ORCID,Smorodina Eva8ORCID,Schubert Thomas9,Azzellino Giovanni5,Jin David10,Kong Jing5ORCID,Palacios Tomás4ORCID,Sleytr Uwe B.7ORCID,Zhang Shuguang2ORCID

Affiliation:

1. State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.

2. MIT Media Lab, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.

3. The David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.

4. Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.

5. Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

6. Chinese Academy of Fishery Sciences, Beijing 100141, China.

7. Department of Bionanosciences (DBNS), BOKU-University of Natural Resources and Life Sciences, Vienna, Austria.

8. Department of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.

9. 2bind GmbH, Am BioPark 11, 93053 Regensburg, Germany.

10. Avalon GloboCare Corp., Freehold, NJ 07728, USA.

Abstract

Affinity-based biosensing can enable point-of-care diagnostics and continuous health monitoring, which commonly follows bottom-up approaches and is inherently constrained by bioprobes’ intrinsic properties, batch-to-batch consistency, and stability in biofluids. We present a biomimetic top-down platform to circumvent such difficulties by combining a “dual-monolayer” biorecognition construct with graphene-based field-effect-transistor arrays. The construct adopts redesigned water-soluble membrane receptors as specific sensing units, positioned by two-dimensional crystalline S-layer proteins as dense antifouling linkers guiding their orientations. Hundreds of transistors provide statistical significance from transduced signals. System feasibility was demonstrated with rSbpA-ZZ/CXCR4 QTY -Fc combination. Nature-like specific interactions were achieved toward CXCL12 ligand and HIV coat glycoprotein in physiologically relevant concentrations, without notable sensitivity loss in 100% human serum. The construct is regeneratable by acidic buffer, allowing device reuse and functional tuning. The modular and generalizable architecture behaves similarly to natural systems but gives electrical outputs, which enables fabrication of multiplex sensors with tailored receptor panels for designated diagnostic purposes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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