A Cytomorphic Chip for Quantitative Modeling of Fundamental Bio-Molecular Circuits

作者：Woo Sung Sik^*; Kim Jaewook; Sarpeshkar Rahul

来源：IEEE Transactions on Biomedical Circuits and Systems, 2015, 9(4): 527-542.

DOI：10.1109/TBCAS.2015.2446431

• Cytomorphic
• molecular circuits
• quantitative cellular models
• reaction networks
• stochastic simulation
• synthetic biology
• systems biology
• transistor models

We describe a 0.35 mu m BiCMOS silicon chip that quantitatively models fundamental molecular circuits via efficient log-domain cytomorphic transistor equivalents. These circuits include those for biochemical binding with automatic representation of non-modular and loading behavior, e.g., in cascade and fan-out topologies; for representing variable Hill-coefficient operation and cooperative binding; for representing inducer, transcription-factor, and DNA binding; for probabilistic gene transcription with analogic representations of log-linear and saturating operation; for gain, degradation, and dynamics of mRNA and protein variables in transcription and translation; and, for faithfully representing biological noise via tunable stochastic transistor circuits. The use of on-chip DACs and ADCs enables multiple chips to interact via incoming and outgoing molecular digital data packets and thus create scalable biochemical reaction networks. The use of off-chip digital processors and on-chip digital memory enables programmable connectivity and parameter storage. We show that published static and dynamic MATLAB models of synthetic biological circuits including repressilators, feed-forward loops, and feedback oscillators are in excellent quantitative agreement with those from transistor circuits on the chip. Computationally intensive stochastic Gillespie simulations of molecular production are also rapidly reproduced by the chip and can be reliably tuned over the range of signal-to-noise ratios observed in biological cells.

• 出版日期2015-8
• 单位MIT