RBS Calculator | De Novo DNA Docs (2024)

Summary

The Ribosome Binding Site (RBS) Calculator is a design algorithm for predicting and controlling translation initiation and protein expression in bacteria across a 100,000-fold range. In Predict mode, the RBS Calculator calculates the translation initiation rate for every start codon in an mRNA transcript. In Design mode, the RBS Calculator generates an optimized synthetic RBS sequence to achieve a targeted translation initiation rate for an inputted protein coding sequence. Additional design constraints can be used to customize the synthetic RBS sequence, for example, to include restriction sites or a constant upstream sequence.

Web Interface Links

RBS Calculator Predict Mode

RBS Calculator Design Mode

RBS Calculator Predict Mode

Inputs

Title: the name of your design job [optional]

mRNA Sequence: the nucleotide sequence of the mRNA transcript, starting from the transcriptional start site and ending at the transcriptional terminator. ATCGU nucleotides allowed.

Host Organism: the bacterial species used to express the protein, selectable from a long list (start typing to narrow down your choices).

Free Energy Model Version: the free energy model used to carry out predictions. New versions are developed as more interactions are quantitatively characterized and incorporated into the model.

Outputs

Translation Initiation Rates: the calculated translation initiation rates for each start codon in the mRNA sequence. The rates are given on a proportional scale ranging from 1 to 100,000+.

Translated Open Reading Frames: a plot showing the translation initiation rates for each protein coding sequence in the mRNA transcript at their respective locations. mRNA transcripts often contain multiple start codons, yielding multiple (potentially overlapping) open reading frames. The open reading frames with the highest translation initiation rates are favored by the ribosome for synthesis of the corresponding proteins.

Ribosome Binding Free Energy Calculations: a detailed table showing the free energy calculations used to predict each start codon's translation initiation rate. Each Gibbs free energy change is the quantification of an interaction between the ribosome and mRNA that affects its translation initiation rate. Read more about the RBS Calculator's free energy model.

RBS Calculator Design Mode

Inputs

Title: the name of your design job [optional]

Protein Coding Sequence: the nucleotide sequence of the protein coding sequence, starting from the start codon and ending at the stop codon. ATCGU nucleotides allowed.

Target Translation Initiation Rate: the desired translation initiation rate for your protein coding sequence, given on a proportional scale from 1 to 100,000+. The maximum possible translation initiation rate is over 5,000,000; however, depending on the protein coding sequence, the maximum rate is not always achievable.

"Goal: Maximize Translation Initiation Rate": check this box to design a synthetic RBS sequence with the highest possible translation initiation rate for your protein coding sequence. Warning: an excessively high translation rate may become toxic to cells, due to ribosome sequestration and metabolic burden.

Host Organism: the bacterial species used to express the protein, selectable from a long list (start typing to narrow down your choices).

Advanced Options

Initial RBS Sequence: sequence used to initialize the design of the synthetic RBS (ATCGU nucleotides allowed). Useful when designing synthetic RBSs with very high translation initiation rates (e.g. entering a previously designed synthetic RBS as the starting point for a new design calculation). [optional]

Constant Upstream Sequence: a nucleotide sequence that appears upstream of the synthetic RBS (ATCGU nucleotides allowed). Useful when adding upstream restriction sites, ribozymes, or any other mRNA sequence (e.g. a long 5' UTR that should remain unchanged). The constant upstream sequence must be part of the mRNA transcript. [optional]

RBS Sequence Constraints: a degenerate nucleotide sequence that controls which nucleotides are allowed to be chosen during RBS design. Degenerate nucleotides follow the nucleotide IUPAC code (ATCGUSRMWKYVBDHN allowed). [optional]

Free Energy Model Version: the free energy model used to carry out predictions. New versions are developed as more interactions are quantitatively characterized and incorporated into the model. [optional]

Outputs

Designed RBS sequence: the ribosome binding site sequence generated by the RBS Calculator. The predicted translation initiation rate is also shown, specifically when this RBS sequence is placed upstream of the specified protein coding sequence.

Translated Open Reading Frames: a plot showing the translation initiation rates for each protein coding sequence in the mRNA transcript at their respective locations. Protein coding sequences often contain multiple start codons, yielding multiple (potentially overlapping) open reading frames. The open reading frames with the highest translation initiation rates are favored by the ribosome for synthesis of the corresponding proteins. It is important to examine this plot to ensure that the specified protein coding sequence does not have any internal start codons with higher translation initiation rates.

mRNA Stability Calculations: the predicted decay rate of the mRNA transcript, assuming that there is only one protein coding sequence in the operon. The calculations consider the sequence and structure of the 5' untranslated region as well as the translation rate of the protein coding sequence. The contributions to the prediction include RNase binding probabilities and the level of ribosome protection (quantified by the average unprotected distance between ribosomes).

Ribosome Binding Free Energy Calculations: a detailed table showing the free energy calculations used to predict each start codon's translation initiation rate. Each Gibbs free energy change is the quantification of an interaction between the ribosome and mRNA that affects its translation initiation rate. Read more about the RBS Calculator's free energy model.

Relevant Articles

Reis, A.C. & Salis, H.M. (2020). An automated model test system for systematic development and improvement of gene expression models. ACS Synthetic Biology, 9(11), 3145-3156.

Cetnar, D. P., & Salis, H. M. (2020). Systematic Quantification of Sequence and Structural Determinants Controlling mRNA stability in Bacterial Operons. bioRxiv.

Espah Borujeni, A., Cetnar, D., Farasat, I., Smith, A., Lundgren, N., & Salis, H. M. (2017). Precise quantification of translation inhibition by mRNA structures that overlap with the ribosomal footprint in N-terminal coding sequences. Nucleic acids research, 45(9), 5437-5448.

Espah Borujeni, A. & Salis, H.M. (2016). Translation initiation is controlled by RNA folding kinetics via a ribosome drafting mechanism. Journal of the American Chemical Society, 138(22), 7016-7023.

Espah Borujeni, A., Channarasappa, A.S., & Salis, H.M. (2013). Translation rate is controlled by coupled trade-offs between site accessibility, selective RNA unfolding and sliding at upstream standby sites. Nucleic acids research, 42(4), 2646-2659.

Salis, H.M., Mirsky, E.A., & Voigt, C.A. (2009). Automated design of synthetic ribosome binding sites to control protein expression. Nature biotechnology, 27(10), 946.

RBS Calculator | De Novo DNA Docs (2024)

FAQs

RBS Calculator | De Novo DNA Docs? ›

Summary. The Ribosome Binding Site

Ribosome Binding Site
A ribosome binding site, or ribosomal binding site (RBS), is a sequence of nucleotides upstream of the start codon of an mRNA transcript that is responsible for the recruitment of a ribosome during the initiation of translation.
https://en.wikipedia.org › wiki › Ribosome-binding_site
(RBS) Calculator is a design algorithm for predicting and controlling translation initiation and protein expression in bacteria across a 100,000-fold range. In Predict mode, the RBS Calculator calculates the translation initiation rate for every start codon
start codon
The start codon is the first codon of a messenger RNA (mRNA) transcript translated by a ribosome. The start codon always codes for methionine in eukaryotes and archaea and a N-formylmethionine (fMet) in bacteria, mitochondria and plastids.
https://en.wikipedia.org › wiki › Start_codon
in an mRNA transcript.

What is the RBS sequence of DNA? ›

A ribosome binding site, or ribosomal binding site (RBS), is a sequence of nucleotides upstream of the start codon of an mRNA transcript that is responsible for the recruitment of a ribosome during the initiation of translation.

What is RBS calculator? ›

Abstract. The Ribosome Binding Site (RBS) Calculator is a design method for predicting and controlling translation initiation and protein expression in bacteria. The method can predict the rate of translation initiation for every start codon in an mRNA transcript.

What is the ribosomal binding site prediction? ›

The Ribosome Binding Site (RBS) Calculator is a predictive design method for controlling translation initiation and protein expression in bacteria (Salis et al., 2009). In its reverse engineering mode, the method predicts the rate of translation initiation for every start codon in an mRNA transcript.

What is the measurement for RBS? ›

Values range for RBS test result

If the level is between 140 and 200 mg/dL, the person is at risk of prediabetes. If the value exceeds more than 200 mg/dL, then the person is diagnosed as being diabetic by the physician.

What are the 4 sequences of DNA? ›

Because there are four naturally occurring nitrogenous bases, there are four different types of DNA nucleotides: adenine (A), thymine (T), guanine (G), and cytosine (C).

What is RBS translation? ›

Ribosomal Binding Site (RBS)

This site, located at the 5' untranslated region (UTR) of the mRNA transcript, regulates protein synthesis based on its sequence and structure.

How do you read a DNA sequence? ›

When we look at a sequence of DNA, we read it in the 5′-3′ direction. The relative positions of genes or other sites along a DNA strand can be described as upstream (towards the 5′ end) or downstream (towards the 3′ end).

What is the normal RBS rate? ›

Normal Results

Most of the time, the blood glucose level will be 125 mg/dL (6.9 mmol/L) or lower. The examples above show the common measurements for results of these tests. Normal value ranges may vary slightly among different laboratories. Some labs use different measurements or may test different specimens.

How to convert DNA sequence to mRNA? ›

The enzyme that converts DNA into mRNA is called RNA polymerase, which attaches to the DNA double helix as shown here. Once attached, RNA polymerase can unwind the helix and begin copying one of the DNA strands to form an mRNA transcript of the gene.

What is RBS count in blood test? ›

A Random blood sugar test (RBS) is a blood test to estimate the level of blood sugar of a non-fasting person. The RBS test is done to diagnose diabetes mellitus. Other names are random glucose tests and casual blood glucose tests (CBG tests). Secure your health with a second opinion.

What are the three ribosomal binding sites? ›

The 3 binding sites for tRNA are called aminoacyl site (abbreviated A), the peptidyl site (abbreviated P) and the exit site (abbreviated E), which are oriented 5' to 3' E-P-A with respect to the mRNA.

Is a ribosome binding site necessary? ›

A ribosome binding site sequence is necessary for efficient expression of the distal gene of a translationally-coupled gene pair.

How far is the ribosome binding site? ›

Upon inspection of the hilA-leader region, a putative RBS can be found approximately 12 nucleotides upstream of the start codon (Fig. 1A). This distance is longer than the optimal 3–9 nucleotides distance between the RBS and the start codon for efficient translational initiation [40,41].

What is the DNA sequence that codes for insulin? ›

This is encoded by a 14kb sequence on the INS gene. In most animals including humans, a single gene for insulin is found. The human gene is located on the short arm of chromosome 11 at position 15.5 (11p15. 5).

What is the reading sequence of DNA? ›

A double-stranded DNA molecule has six reading frames. Both strands are read in the 5′→3′ direction. Each strand has three reading frames, depending on which nucleotide is chosen as the starting position. The key to the success of ORF scanning is the frequency with which termination codons appear in the DNA sequence.

What is an SD sequence? ›

This ribosomal binding site in bacterial messenger RNA became known as the Shine-Dalgarno (SD) sequence. It enables initiation of protein synthesis by aligning the ribosome with the start codon. Simply put, genes are read in groups of three letters, but you need to let the ribosome know where to start.

What is the DNA content of RBC? ›

Mature RBCs do not have a nucleus or DNA. However, WBC (leukocytes) have DNA.

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