Difference between revisions of "Protein domains"

Revision as of 23:11, 11 January 2009

Protein domains encode portions of proteins and can be assembled together to form translational units, a genetic part spanning from translational initiation (the RBS) to translational termination (the stop codon).

There are several different types of protein domains.

Head Domain: The Head domain consists of the start codon followed immediately by zero or more triplets specifiying an N-terminal tag, such as a protein export tag or lipoprotein binding tag. Head domains should begin with an ATG start codon and include codons 2 and 3 of the protein at a minimum. Examples of head domains include
- ATG start codon
- ATG start codon and codons 2-3
- ATG start codon and signal sequence
- ATG start codon and affinity tag
Internal Domains: Protein domains consist of a series of codon triplets coding for an amino acid sequence without a start codon or stop codon. Multiple Internal Domains can be fused. Examples of internal domains include
- DNA binding domains
- Dimerization domains
- Kinase domains
Special Internal Domains: Short Domains with specific function may be separately categorized, but obey the same composition rules as normal internal domains. Examples of special internal domains include
- Linkers
- Cleavage sites
- Inteins
Tail Domain: The C-terminus of a coding region consists of zero or more triplet codons, followed by a pair of TAA stop codons. In the simplest case, the stop codons terminate the protein with an Stop. More complex Tails may include degradation tags appropriate to the organism (i.e., with different degradation rates). Examples of Tail domain include
- TAATAA stop codons
- A degradation tag followed by TAATAA stop codons
- An affinity tag followed by TAATAA stop codon

Unfortunately, the original BioBrick assembly standard, Assembly standard 10, does not support in-frame assembly of protein domains. (Assembly standard 10 creates an 8 bp scar between adjacent parts.) Therefore, it is recommended that you use an alternate approach to assemble protein domains together to make a translational unit. There are several possible approaches to assembling protein domains including direct synthesis (preferred because it creates no scars) as well as various assembly standards. Regardless of which standard you choose, we suggest that the resulting protein coding sequence or translational unit comply with the original BioBrick assembly standard so that your parts can be assembled with most of the parts in the Registry.

Protein coding sequences should be as follows

GAATTC GCGGCCGC T TCTAG [ATG ... TAA TAA] T ACTAGT A GCGGCCG CTGCAG

Note: Although most RBSs are currently specified as separate parts in the Registry, we are now moving to a new design in which the RBS and Head domain are combined into a single part termed a Translational start. The new design has the advantage of encapsulating both ribosome binding and translational initiation within a single part. Our working hypothesis is that the new design will reduce the likelihood of unexpected functional composition problems between the RBS and coding sequence.

	Localization signals: Short protein sequences that "tell" a cell where to send a protein. For example, a localization sequence might send a protein to the nucleus or mark it for secretion outside of the cell.
	Affinity tags: Short protein sequences or protein domains that can bind to antibody, metal ion, or other substrate. Generally, affinity tags are fused to proteins to enable purification via binding to an immobilized ligand or quantification via western blot.
	Linkers: Short protein sequences used to link or fuse two protein domains together.
	Degradation tags: Short protein sequences or protein domains that target a protein for degradation by cellular machinery thereby increasing protein turnover and decreasing protein half-life. Since most degradation tags rely on endogenous cellular machinery for degradation, degradation tags are specific to particular chassis.
	Cleavage sites: Short protein sequences or motifs that are recognized by site-specific proteases that then cut a particular peptide bond.
	Help: A glossary, FAQ, and further reading on protein tags and modifiers.

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 |align='center' width=80px | {{Click || image=Proteinaffinitytagbutton.png | link=Protein tags and modifiers/Affinity|width=50px | height=50px }} |'''[[Protein tags and modifiers/Affinity|Affinity tags]]''': Short protein sequences or protein domains that can bind to antibody, metal ion, or other substrate.  Generally, affinity tags are fused to proteins to enable purification via binding to an immobilized ligand or quantification via western blot.
 |-
-|align='center' width=80px | {{Click || image=Registrylist.png | link=Protein tags and modifiers/Fusion|width=50px | height=50px }} |'''[[Protein tags and modifiers/Fusion|Linkers]]''':  Short protein sequences used to link or fuse two protein domains together.
+|align='center' width=80px | {{Click || image=RegistryList.png | link=Protein tags and modifiers/Fusion|width=50px | height=50px }} |'''[[Protein tags and modifiers/Fusion|Linkers]]''':  Short protein sequences used to link or fuse two protein domains together.
 |-
 |align='center' width=80px | {{Click || image=Plasmidnonbiobrickvectorsbutton.png | link=Protein tags and modifiers/Degradation|width=50px | height=50px }} |'''[[Protein tags and modifiers/Degradation|Degradation tags]]''':  Short protein sequences or protein domains that target a protein for degradation by cellular machinery thereby increasing protein turnover and decreasing protein half-life.  Since most degradation tags rely on endogenous cellular machinery for degradation, degradation tags are specific to particular chassis.