Self-assembled GA-Repeated Peptides as a Biomolecular Scaffold for Biosensing with MoS(2) Electrochemical Transistors

[Image: see text] Biosensors with two-dimensional materials have gained wide interest due to their high sensitivity. Among them, single-layer MoS(2) has become a new class of biosensing platform owing to its semiconducting property. Immobilization of bioprobes directly onto the MoS(2) surface with chemical bonding or random physisorption has been widely studied. However, these approaches potentially cause a reduction of conductivity and sensitivity of the biosensor. In this work, we designed peptides that spontaneously align into monomolecular-thick nanostructures on electrochemical MoS(2) transistors in a non-covalent fashion and act as a biomolecular scaffold for efficient biosensing. These peptides consist of repeated domains of glycine and alanine in the sequence and form self-assembled structures with sixfold symmetry templated by the lattice of MoS(2). We investigated electronic interactions of self-assembled peptides with MoS(2) by designing their amino acid sequence with charged amino acids at both ends. Charged amino acids in the sequence showed a correlation with the electrical properties of single-layer MoS(2), where negatively charged peptides caused a shift of threshold voltage in MoS(2) transistors and neutral and positively charged peptides had no significant effect on the threshold voltage. The transconductance of transistors had no decrease due to the self-assembled peptides, indicating that aligned peptides can act as a biomolecular scaffold without degrading the intrinsic electronic properties for biosensing. We also investigated the impact of peptides on the photoluminescence (PL) of single-layer MoS(2) and found that the PL intensity changed sensitively depending on the amino acid sequence of peptides. Finally, we demonstrated a femtomolar-level sensitivity of biosensing using biotinylated peptides to detect streptavidin.