4.8 Article

Denaturing for Nanoarchitectonics: Local and Periodic UV-Laser Photodeactivation of Protein Biolayers to Create Functional Patterns for Biosensing

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 36, Pages 41640-41648

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c12808

Keywords

biosensor; UV denaturation; immunoassay; non-specific binding; label-free; diffraction

Funding

  1. Ministerio de Ciencia e Innovacion/Agencia Estatal de Investigacion [MCIN/AEI/10.13039/501100011033]
  2. European Union [PID2019-110713RB-I00, PDI2019-104276RB-I00]
  3. Generalitat Valenciana [PROMETEO/2020/094, PROMETEO/2019/048]
  4. FPI-UPV 2017 grant program

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In this work, a photopatterning method based on UV-laser irradiation is presented to create periodic structures of biomacromolecules by inducing local and mild denaturation of protein biolayers. The resulting nanostructures exhibit a periodic modulation of protein activity, making them suitable for application in diffractive biosensing. The study shows that this UV-based patterning principle is an easy, cost-effective, and fast way to fabricate large areas of homogeneous one-dimensional protein patterns, and these patterns can effectively be used as transducers for biosensing applications.
The nanostructuration of biolayers has become a paradigm for exploiting nanoscopic light-matter phenomena for biosensing, among other biomedical purposes. In this work, we present a photopatterning method to create periodic structures of biomacromolecules based on a local and periodic mild denaturation of protein biolayers mediated by UV-laser irradiation. These nanostructures are constituted by a periodic modulation of the protein activity, so they are free of topographic and compositional changes along the pattern. Herein, we introduce the approach, explore the patterning parameters, characterize the resulting structures, and assess their overall homogeneity. This UV-based patterning principle has proven to be an easy, cost-effective, and fast way to fabricate large areas of homogeneous one-dimensional protein patterns (2 min, 15 x 1.2 mm, relative standard deviation ? 16%). This work also investigates the implementation of these protein patterns as transducers for diffractive biosensing. Using a model immunoassay, these patterns have demonstrated negligible signal contributions from non-specific bindings and comparable experimental limits of detection in buffer media and in human serum (53 and 36 ng & BULL;mL-1 of unlabeled IgG, respectively).

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