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Biology subjects

Lale, R.

Publications and source records attributed to Lale, R..

4 recordsLinked to original sources

From Context to Code: Rational De Novo DNA Design and Predicting Cross-Species DNA Functionality Using Deep Learning Transformer Models

Synthetic biology currently operates under a framework dominated by trial-and-error approaches, which hinders the effective engineering of organisms and the expansion of large-scale biomanufacturing. Motivated by the success of computational designs in areas like architecture and aeronautics, we aspire to transition to a more efficient and predictive methodology in synthetic biology. In this study, we report a DNA Design Platform that relies on the predictive power of Transformer-based deep learning architectures. The platform transforms the conventional paradigms in synthetic biology by enabling the context-sensitive and host-specific engineering of 5' regulatory elements--promoters and 5' untranslated regions (UTRs) along with an array of codon-optimised coding sequence (CDS) variants. This allows us to generate context-sensitive 5' regulatory sequences and CDSs, achieving an unparalleled level of specificity and adaptability in different target hosts. With context-aware design, we significantly broaden the range of possible gene expression profiles and phenotypic outcomes, substantially reducing the need for laborious high-throughput screening efforts. Our context-aware, AI-driven design strategy marks a significant advancement in synthetic biology, offering a scalable and refined approach for gene expression optimisation across a diverse range of expression hosts. In summary, this study represents a substantial leap forward in the field, utilising deep learning models to transform the conventional design, build, test, learn-cycle into a more efficient and predictive framework.

synthetic biology↗

mCherry contains a fluorescent protein isoform that interferes with its reporter function

Fluorescent proteins are essential reporters in cell biology and molecular biology. Here, we reveal that red-fluorescent proteins possess an alternative translation initiation site that produces a short functional protein isoform. The short isoform creates significant background fluorescence that biases the outcome of expression studies. Our investigation identifies the short protein isoform, traces its origin, and determines the extent of the issue within the family of red fluorescent protein. Our analysis shows that the short isoform defect of the red fluorescent protein family may affect the interpretation of many published studies. Finally, we provide a re-engineered mCherry variant that lacks background expression as an improved tool for imaging and protein expression studies.

molecular biology↗

Dual UTR-A novel 5′ untranslated region design for synthetic biology applications

Bacterial 5' untranslated regions of mRNA (UTR) involve in a complex regulation of gene expression; however, the exact sequence features contributing to gene regulation are not yet fully understood. In this study, we report the design of a novel 5' UTR, dual UTR, utilising the transcriptional and translational characteristics of 5' UTRs in a single expression cassette. The dual UTR consists of two 5' UTRs, each separately leading to either increase in transcription or translation of the reporter, that are separated by a spacer region, enabling de novo translation initiation. We rationally create dual UTRs with a wide range of expression profiles and demonstrate the functionality of the novel design concept in Escherichia coli and in Pseudomonas putida using different promoter systems and coding sequences. Overall, we demonstrate the application potential of dual UTR design concept in various synthetic biology applications ranging from fine-tuning of gene expression to maximisation of protein production.

synthetic biology↗

A universal method for gene expression engineering

The precise expression of genes is one of the foundations of biotechnology. Here we present GeneEE, a straightforward method for generating artificial gene expression systems. We demonstrate that GeneEE segments, containing a 200 nucleotide DNA with random nucleotide composition, can facilitate constitutive and inducible gene expression. To highlight the universal character of our method, we demonstrate GeneEE-mediated gene and protein expression in six bacterial species and Bakers yeast.

bioengineering↗