Abstract
Biomolecular systems for information processing have recently received great attention in the general framework of unconventional computing. While DNA biocomputing systems have been studied by many researchers and have already reached a high level of complexity, enzyme-based cascades mimicking Boolean logic operations are a relatively new subfield that is rapidly progressing. This chapter reviews recent progress in the enzyme-based information processing systems and suggests applications in biosensing, rather than computation. This chapter overviews various methods for analysis of output signals generated by enzyme-based logic systems. The considered methods include different optical techniques (optical absorbance, fluorescence spectroscopy, surface plasmon resonance), electrochemical techniques (cyclic voltammetry, potentiometry, impedance spectroscopy, conductivity measurements, use of field-effect transistor devices, pH measurements), and various mechano-electronic methods (using atomic force microscope, quartz crystal microbalance). While each of the methods is already well known for various bioanalytical applications, their use in combination with the biomolecular logic systems is rather new and sometimes not trivial. Many of the discussed methods have been combined with the use of signal-responsive materials to transduce and amplify biomolecular signals generated by the logic operations. Interfacing of biocomputing logic systems with electronics and “smart” signal-responsive materials allowed for extending logic operations to actuation functions, for example, stimulating molecular release and switchable features of bioelectronic devices, such as biofuel cells. The purpose of this chapter is to emphasize broad variability of the bioanalytical systems applied for the signal transduction in biocomputing processes. All bioanalytical systems discussed in the article are exemplified with specific logic gates and multi-gate networks realized with enzyme-based biocatalytic cascades.
This chapter is based partially on recently published review articles (Katz 2015, 2017; Katz et al. 2017) with the copyright permissions from Elsevier, Wiley-VCH, and Springer. The compiled text was updated and edited.
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Abbreviations
- Abs:
-
Optical absorbance
- ABTS:
-
2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (chromogenic substrate used to follow peroxidase activity)
- ABTSox :
-
Oxidized ABTS (colored product)
- Ac:
-
Acetic acid
- AcCh:
-
Acetylcholine
- AcChE:
-
Acetylcholinesterase (enzyme; EC 3.1.1.7)
- ADH:
-
Alcohol dehydrogenase (enzyme; EC 1.1.1.1)
- ADP:
-
Adenosine 5′-diphosphate
- AFM:
-
Atomic force microscope (microscopy)
- AGS:
-
Amyloglucosidase (enzyme; EC 3.2.1.3)
- Ala:
-
Alanine (amino acid)
- Ald:
-
Acetaldehyde
- ALT:
-
Alanine transaminase (enzyme; EC 2.6.1.2)
- Asc:
-
Ascorbic acid
- ATP:
-
Adenosine 5′-triphosphate
- BuCh:
-
Butyrylcholine
- ChO:
-
Choline oxidase (enzyme; EC 1.1.3.17)
- CK:
-
Creatine kinase (enzyme; EC 2.7.3.2)
- CN:
-
4-Chloro-1-naphthol
- CN-ox:
-
CN insoluble oxidized product
- Crt:
-
Creatine
- DC:
-
Direct current
- DHA:
-
dehydroascorbic acid (product of oxidation of ascorbic acid)
- Diaph:
-
Diaphorase (enzyme; EC 1.8.1.4)
- DNA:
-
Deoxyribonucleic acid
- EIS:
-
Electrolyte–insulator–semiconductor
- Et-O-Ac:
-
Ethyl acetate
- EtOH:
-
Ethanol
- FET:
-
Field-effect transistor
- Frc:
-
Fructose
- G6PDH:
-
Glucose 6-phosphate dehydrogenase (enzyme; EC 1.1.1.49)
- GDH:
-
Glucose dehydrogenase (enzyme; EC 1.1.1.47)
- Glc:
-
Glucose
- Glc6P:
-
Glucose-6-phosphate
- Glc6PA:
-
Gluconate-6-phosphate acid (product of Glc6P oxidation)
- GlcA:
-
Gluconic acid
- Glu:
-
Glutamate (amino acid, salt form)
- GluOx:
-
Glutamate oxidase (enzyme; EC 1.4.3.11)
- GOx:
-
Glucose oxidase (enzyme; EC 1.1.3.4)
- HK:
-
Hexokinase (enzyme; EC 2.7.1.1)
- HRP:
-
Horseradish peroxidase (enzyme; EC 1.11.1.7)
- Inv:
-
Invertase (enzyme; EC 3.2.1.26)
- Ip :
-
Peak current (measured with cyclic voltammetry)
- IR:
-
Infrared
- ITO:
-
Indium tin oxide (electrode)
- Lac:
-
Lactate
- LDH:
-
Lactate dehydrogenase (enzyme; EC 1.1.1.27)
- LSPR:
-
Localized surface plasmon resonance
- Luc:
-
Luciferase (enzyme from ATP assay kit, Sigma-Aldrich)
- Lucif:
-
Luciferin
- MP-11:
-
Microperoxidase-11
- MPh:
-
Maltose phosphorylase (enzyme; EC 2.4.1.8)
- NAD+ :
-
Nicotinamide adenine dinucleotide
- NADH:
-
Nicotinamide adenine dinucleotide reduced
- NPs:
-
Nanoparticles
- O/W:
-
Oil-in-water Pickering emulsion
- P2VP:
-
Poly(2-vinylpyridine)
- P4VP:
-
Poly(4-vinylpyridine)
- PB:
-
Prussian blue
- PEO:
-
Poly(ethylene oxide)
- PEP:
-
Phospho(enol)pyruvic acid (or phosphoenolpyruvate in the form of salt)
- Pi:
-
Inorganic phosphate
- PK:
-
Pyruvate kinase (enzyme; EC 2.7.1.40)
- Ppy:
-
Polypyrrole
- Ppy-ox:
-
Polypyrrole-oxidized state
- Ppy-red:
-
Polypyrrole-reduced state
- PQQ:
-
Pyrroloquinoline quinone
- PS:
-
Polystyrene
- Pyr:
-
Pyruvate
- QCM:
-
Quartz crystal microbalance
- R:
-
Reflectance measured by SPR
- Rcell :
-
Ohmic resistance measured in a bulk solution in an electrochemical cell
- RE:
-
Reference electrode
- Ret :
-
Electron transfer resistance (measured by Faradaic impedance spectroscopy)
- RNA:
-
Ribonucleic acid
- SPR:
-
Surface plasmon resonance
- TBI:
-
Traumatic brain injury
- TMB:
-
3,3′,5,5′-Tetramethylbenzidine (chromogenic substrate used to follow peroxidase activity)
- UV:
-
Ultraviolet
- Va :
-
Alternative voltage applied between the conducting support and reference electrode of the EIS devise
- Vbias :
-
Constant (bias) voltage applied between the conducting support and reference electrode of the EIS devise
- VFB :
-
Flat band voltage of the EIS device
- W/O:
-
Water-in-oil Pickering emulsion
- α-KTG:
-
α-Ketoglutaric acid
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Katz, E. (2017). Enzyme-Based Logic Systems: Composition, Operation, Interfacing, and Applications. In: Meyers, R. (eds) Encyclopedia of Complexity and Systems Science. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-27737-5_681-1
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