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      Nanobio Interface Between Proteins and 2D Nanomaterials

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          Abstract

          Two-dimensional (2D) nanomaterials have significantly contributed to recent advances in material sciences and nanotechnology, owing to their layered structure. Despite their potential as multifunctional theranostic agents, the biomedical translation of these materials is limited due to a lack of knowledge and control over their interaction with complex biological systems. In a biological microenvironment, the high surface energy of nanomaterials leads to diverse interactions with biological moieties such as proteins, which play a crucial role in unique physiological processes. These interactions can alter the size, surface charge, shape, and interfacial composition of the nanomaterial, ultimately affecting its biological activity and identity. This review critically discusses the possible interactions between proteins and 2D nanomaterials, along with a wide spectrum of analytical techniques that can be used to study and characterize such interplay. A better understanding of these interactions would help circumvent potential risks and provide guidance toward the safer design of 2D nanomaterials as a platform technology for various biomedical applications.

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          Electric Field Effect in Atomically Thin Carbon Films

          We describe monocrystalline graphitic films, which are a few atoms thick but are nonetheless stable under ambient conditions, metallic, and of remarkably high quality. The films are found to be a two-dimensional semimetal with a tiny overlap between valence and conductance bands, and they exhibit a strong ambipolar electric field effect such that electrons and holes in concentrations up to 10 13 per square centimeter and with room-temperature mobilities of ∼10,000 square centimeters per volt-second can be induced by applying gate voltage.
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            Two-dimensional nanocrystals produced by exfoliation of Ti3 AlC2.

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              Measurement of the elastic properties and intrinsic strength of monolayer graphene.

              We measured the elastic properties and intrinsic breaking strength of free-standing monolayer graphene membranes by nanoindentation in an atomic force microscope. The force-displacement behavior is interpreted within a framework of nonlinear elastic stress-strain response, and yields second- and third-order elastic stiffnesses of 340 newtons per meter (N m(-1)) and -690 Nm(-1), respectively. The breaking strength is 42 N m(-1) and represents the intrinsic strength of a defect-free sheet. These quantities correspond to a Young's modulus of E = 1.0 terapascals, third-order elastic stiffness of D = -2.0 terapascals, and intrinsic strength of sigma(int) = 130 gigapascals for bulk graphite. These experiments establish graphene as the strongest material ever measured, and show that atomically perfect nanoscale materials can be mechanically tested to deformations well beyond the linear regime.
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                Author and article information

                Journal
                ACS Appl Mater Interfaces
                ACS Appl Mater Interfaces
                am
                aamick
                ACS Applied Materials & Interfaces
                American Chemical Society
                1944-8244
                1944-8252
                24 July 2023
                02 August 2023
                : 15
                : 30
                : 35753-35787
                Affiliations
                []School of Biosciences and Bioengineering, Indian Institute of Technology , Mandi, Kamand, Mandi, Himachal Pradesh 175075, India
                []Department of Biomedical Engineering, College of Engineering, Texas A&M University , College Station, Texas 77843, United States
                [§ ]Interdisciplinary Graduate Program in Genetics and Genomics, Texas A&M University , College Station, Texas 77843, United States
                Author notes
                Author information
                https://orcid.org/0000-0002-2233-383X
                https://orcid.org/0000-0002-0284-0201
                https://orcid.org/0000-0002-9748-0404
                Article
                10.1021/acsami.3c04582
                10866197
                37487195
                0174e4b3-bb25-4a4f-93cf-87c7b22b740d
                © 2023 American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 30 March 2023
                : 22 June 2023
                Funding
                Funded by: U.S. Department of Defense, doi 10.13039/100000005;
                Award ID: W81XWH2210932
                Funded by: Department of Science and Technology, Ministry of Science and Technology, India, doi 10.13039/501100001409;
                Award ID: NA
                Funded by: Texas A and M University, doi 10.13039/100007904;
                Award ID: NA
                Funded by: United States - India Educational Foundation, doi 10.13039/100006222;
                Award ID: NA
                Funded by: National Institute of Biomedical Imaging and Bioengineering, doi 10.13039/100000070;
                Award ID: DP2 EB026265
                Categories
                Review
                Custom metadata
                am3c04582
                am3c04582

                Materials technology
                2d nanomaterial,protein corona,surface energy,interaction forces,analytical tools

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