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Gobry, M. V.

Publications and source records attributed to Gobry, M. V..

2 recordsLinked to original sources

Modular RNA motifs for orthogonal phase separated compartments

Recent discoveries in biology have highlighted the importance of protein and RNA-based condensates as an alternative to classical membrane-bound organelles for the task of compartmentalizing molecules and biochemical reactions. Here, we demonstrate the rational design of pure RNA condensates from star-shaped RNA motifs. We generate condensates using two different RNA nanostar architectures: multi-stranded nanostars whose binding interactions are programmed via single-stranded overhangs, and single-stranded nanostars whose interactions are programmed via kissing loops. Through rational design of the nanostar interaction sequences, we demonstrate that both architectures can produce orthogonal (distinct and immiscible) condensates, which can be individually tracked via fluorogenic aptamers. We also show that aptamers make it possible to recruit peptides and proteins to the condensates with high specificity. Successful cotranscriptional formation of condensates from single-stranded nanostars suggests that they may be genetically encoded and produced in living cells. We provide a library of orthogonal RNA condensates that can be modularly customized and offer a route toward creating systems of functional artificial organelles.

synthetic biology↗

Enzymatic assembly of small synthetic genes with repetitive elements

Gene synthesis efficiency has greatly improved in recent years but is limited when it comes to repetitive sequences and results in synthesis failure or delays by DNA synthesis vendors. This is representing a major obstacle for the development of synthetic biology, since repetitive elements are increasingly being used in design of genetic circuits and design of biomolecular nanostructures. Here, we describe a method for the assembly of small synthetic genes with repetitive elements: First, a gene of interest is split in silico into small synthons of up to 80 base pairs flanked by Golden Gate-compatible overhangs. Then, synthons are made by oligo extension and finally assembled into a synthetic gene by Golden Gate Assembly. We demonstrate the method by constructing eight challenging genes with repetitive elements e.g., multiple repeats of RNA aptamers and RNA origami scaffolds with multiple identical aptamers. The genes range in size from 133 to 456 base pairs and are assembled with fidelities of up to 87.5 %. The method was developed to facilitate our own specific research but may be of general use for constructing challenging and repetitive genes and thus a valuable addition to the molecular cloning toolbox.

synthetic biology↗