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Controlled Surface Silanization for Actin-Myosin and Biocompatibility of New Polymer Resists
Lund University.ORCID-id: 0000-0001-5617-6337
Linnéuniversitetet, Fakulteten för Hälso- och livsvetenskap (FHL), Institutionen för kemi och biomedicin (KOB).
Linnéuniversitetet, Fakulteten för Hälso- och livsvetenskap (FHL), Institutionen för kemi och biomedicin (KOB).ORCID-id: 0000-0002-2797-2294
Linnéuniversitetet, Fakulteten för Hälso- och livsvetenskap (FHL), Institutionen för kemi och biomedicin (KOB).ORCID-id: 0000-0003-4835-0598
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2018 (Engelska)Ingår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 34, nr 30, s. 8777-8784Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Molecular motor-based nanodevices require organized cytoskeletal filament guiding along motility-promoting tracks, confined by motility-inhibiting walls. One way to enhance motility quality on the tracks, particularly in terms of filament velocity but also the fraction of motile filaments, is to optimize the surface hydrophobicity. We have investigated the potential to achieve this for the actin myosin II motor system on trimethylchlorosilane (TMCS)-derivatized SiO2 surfaces to be used as channel floors in nanodevices. We have also investigated the ability to supress motility on two new polymer resists, TU7 (for nanoimprint lithography) and CSAR 62 (for electron beam and deep UV lithography), to be used as channel walls. We developed a chemical-vapor deposition tool for silanizing SiO2 surfaces in a controlled environment to achieve different surface hydrophobicities (measured by water contact angle). In contrast to previous work, we were able to fabricate a wide range of contact angles by varying the silanization time and chamber pressure using only one type of silane. This resulted in a significant improvement of the silanization procedure, producing a predictable contact angle on the surface and thereby predictable quality of the heavy meromyosin (HMM)-driven actin motility with regard to velocity. We observed a high degree of correlation between the filament sliding velocity and contact angle in the range 10-86 degrees, expanding the previously studied range. We found that the sliding velocity on TU7 surfaces was superior to that on CSAR 62 surfaces despite similar contact angles. In addition, we were able to suppress the motility on both TU7 and CSAR 62 by plasma oxygen treatment before silanization. These results are discussed in relation to previously proposed surface adsorption mechanisms of HMM and their relationship to the water contact angle. Additionally, the results are considered for the development of actin-myosin based nanodevices with superior performance with respect to actin-myosin functionality.

Ort, förlag, år, upplaga, sidor
American Chemical Society (ACS), 2018. Vol. 34, nr 30, s. 8777-8784
Nationell ämneskategori
Biofysik Biokemi och molekylärbiologi
Forskningsämne
Kemi, Biokemi
Identifikatorer
URN: urn:nbn:se:lnu:diva-77391DOI: 10.1021/acs.langmuir.8b01415ISI: 000440768400007PubMedID: 29969272Scopus ID: 2-s2.0-85049637573OAI: oai:DiVA.org:lnu-77391DiVA, id: diva2:1243047
Tillgänglig från: 2018-08-30 Skapad: 2018-08-30 Senast uppdaterad: 2019-08-29Bibliografiskt granskad

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Norrby, MarleneRahman, Mohammad A.Salhotra, AseemTakatsuki, HideyoMånsson, Alf

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Lindberg, Frida W.Norrby, MarleneRahman, Mohammad A.Salhotra, AseemTakatsuki, HideyoMånsson, Alf
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Institutionen för kemi och biomedicin (KOB)
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BiofysikBiokemi och molekylärbiologi

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