Melbourne/Blue Photosensor Background
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[[Melbourne/Background|<return to top of background>]] [[melbourne|<return to home page>]] | [[Melbourne/Background|<return to top of background>]] [[melbourne|<return to home page>]] | ||
- | ==== | + | The background to the design of the blue photosensor is included here. Specifically the design for the chimeric fusion protein that will be the key link in blue light pathway |
- | + | ||
- | [[Melbourne/Blue Photosensor Background/SopII/DNA|DNA]], | + | |
- | [[Melbourne/Blue Photosensor Background/SopII/AA|AA]] | + | == Preliminaries == |
+ | === Tools used=== | ||
+ | Restriction Site Analysis - [http://tools.neb.com/NEBcutter2/index.php| NEB cutter] | ||
+ | |||
+ | Sequence Translation - [http://au.expasy.org/tools/dna.html| Translate] | ||
+ | |||
+ | Sequence Aligment - [http://www.jalview.org/download.html| JalView] | ||
+ | These were done via known domain databases from GenBank, with a ClustalW Realignment option in the Web Services menu of JalView | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/JalView Clustal| Clustal Color Scheme ]] | ||
+ | * [[Melbourne/Blue Photosensor Background/JalView Hydrophobicity| Hydrophobicity Color Scheme ]] | ||
+ | * [[Melbourne/Blue Photosensor Background/JalView Helix Propensity| Helix Propensity Color Scheme ]] | ||
+ | * [[Melbourne/Blue Photosensor Background/JalView Turn Propensity| Turn Propensity Color Scheme ]] | ||
+ | |||
+ | PCR primer design - [http://www.premierbiosoft.com/netprimer/netprlaunch/netprlaunch.html| NetPrimer] | ||
+ | |||
+ | Transmembrane Prediction - [http://www.sbc.su.se/~miklos/DAS/| DAS Transmembrane Prediction] | ||
+ | |||
+ | [[Media:comparison.jar| JalView File of Seq. Alignments ]] - doesn't work ATM | ||
+ | |||
+ | ==Sequences and Restriction Sites== | ||
+ | |||
+ | ==== SopII (sensory rhodopsin II)==== | ||
+ | |||
+ | [[Melbourne/Blue Photosensor Background/SopII/DNA| DNA]], | ||
+ | [[Melbourne/Blue Photosensor Background/SopII/AA| AA]], | ||
[http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | ||
* No IGEM restriction sites | * No IGEM restriction sites | ||
- | * HaeII | + | * HaeII (@168) present |
- | HtrII | + | |
- | [[Melbourne/Blue Photosensor Background/HtrIIA|DNA]], | + | ==== HtrII (sensory rhodopsin II transducer)==== |
- | [[Melbourne/Blue Photosensor Background/HtrII/AA|AA]] | + | |
+ | [[Melbourne/Blue Photosensor Background/HtrIIA| DNA]], | ||
+ | [[Melbourne/Blue Photosensor Background/HtrII/AA| AA]], | ||
[http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3702851&ordinalpos=1&itool=EntrezSystem2.PEntrez.Gene.Gene_ResultsPanel.Gene_RVDocSum genbank] | [http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3702851&ordinalpos=1&itool=EntrezSystem2.PEntrez.Gene.Gene_ResultsPanel.Gene_RVDocSum genbank] | ||
* No IGEM restriction sites | * No IGEM restriction sites | ||
* No useful restriction site | * No useful restriction site | ||
- | SopII/HtrII fusion | + | ==== SopII/HtrII fusion ==== |
- | [[Melbourne/Blue Photosensor Background/Fusion/DNA|DNA]], | + | |
- | [[Melbourne/Blue Photosensor Background/Fusion/AA|AA]] (frame 2 in Translate) | + | [[Melbourne/Blue Photosensor Background/Fusion/DNA| DNA]], |
+ | [[Melbourne/Blue Photosensor Background/Fusion/AA| AA]] (frame 2 in Translate - only SopII + HtrII + Linker included in link), linker = TSASA | ||
+ | SNGASA, | ||
+ | |||
[http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | ||
* No IGEM restriction sites | * No IGEM restriction sites | ||
* Use site from SopII (this is the one that will be used) | * Use site from SopII (this is the one that will be used) | ||
+ | ==== ComP (two-component sensor histidine kinase)==== | ||
- | + | [[Melbourne/Blue Photosensor Background/ComP/DNA| DNA]] (includes IGEM forward and reverse primers (VF2 + VR) and IGEM prefix and suffix, | |
- | [[Melbourne/Blue Photosensor Background/ComP/DNA|DNA]], | + | [[Melbourne/Blue Photosensor Background/ComP/AA| AA]], |
- | [[Melbourne/Blue Photosensor Background/ComP/AA|AA]] | + | |
[http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | ||
- | |||
- | |||
+ | [[Melbourne/primary_Restriction_enzymes| SpeI]] (@927) deleted | ||
+ | [[Melbourne/primary_Restriction_enzymes| HaeII]] (@1902) inserted | ||
- | ComA | + | ==== ComA (sensory rhodopsin II transducer)==== |
- | [[Melbourne/Blue Photosensor Background/ComA/DNA|DNA]], | + | |
- | [[Melbourne/Blue Photosensor Background/ComA/AA|AA]] | + | [[Melbourne/Blue Photosensor Background/ComA/DNA| DNA]], |
+ | [[Melbourne/Blue Photosensor Background/ComA/AA| AA]], | ||
[http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank] | ||
- | [[Melbourne/primary_Restriction_enzymes|SpeI]] (@12) deleted | + | |
- | [[Melbourne/primary_Restriction_enzymes|HaeII]] (@433) inserted | + | [[Melbourne/primary_Restriction_enzymes| SpeI]] (@12) deleted |
+ | [[Melbourne/primary_Restriction_enzymes| HaeII]] (@433) inserted | ||
+ | |||
+ | |||
+ | == Chimera Design == | ||
+ | |||
+ | ==== Overview ==== | ||
+ | |||
+ | Chimera will be constructed using a PCR based stitching approach as described by Spudich, [[Melb:Blue_Photosensor#References|(refer to reference)]] | ||
+ | |||
+ | ==== Analysis of SopII motifs ==== | ||
+ | |||
+ | transmembrane photoreceptor, requires all-trans retinal as substrate... linked to HtrII | ||
+ | insert TM analysis here. reference the three papers cited in background | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/sopII_TM| SopII Transmembrane prediction ]] | ||
+ | |||
+ | This shows consistent TM helicies throughout the whole sequence | ||
+ | |||
+ | ==== Analysis of HtrII motifs ==== | ||
+ | |||
+ | Methyl-accepting chemotaxis proteins (MCP) are hypothesized to be modular in structure (ref needed). This modularity and homology between most MCPs is evidence by the clear separation of HAMP domains from methyl-accepting helical domains and the sensor kinases. Below is shown evidence for this in HtrII. | ||
+ | |||
+ | [[Melbourne/Blue Photosensor Background/HtrII_BLAST| '''HtrII BLAST analysis''' ]] | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/MCP_structure| Hypothesized MCP structure ]] | ||
+ | |||
+ | |||
+ | |||
+ | This hisitidine kinase also has a clear TM region, from residues 0-80 | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/HtrII Transmembrane| HtrII TM finder plot ]] | ||
+ | |||
+ | |||
+ | Genbank mentions the HAMP domain (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) | ||
+ | |||
+ | This is the key to the propagation of the excitation signal according to (ref needed) | ||
+ | |||
+ | Evidence for the HAMP domain is contained in the following sequence alignment with known HAMP domains from GenBank | ||
+ | * [[Melbourne/Blue Photosensor Background/HtrII HAMP| HtrII-pfam00672 Jalview alignment]] | ||
+ | This alignment suggest homogoly from residue 65 to 134 in the HtrII sequence. This conforms with the GenBank analysis shown below. | ||
+ | |||
+ | |||
+ | Evidence for methyl-accepting chemo-taxis like domain (these are the likely helices (hydrophobic residue every 7 AA, after the HAMP domain)) | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/HtrII MCPa| HtrII-Methyl-accepting chemotaxis proteins(MCP)sequence alignment residues 390-490 ]] | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/HtrII MCPb| residues 490-590 ]] | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/HtrII MCPc| residues 590-700 ]] | ||
+ | |||
+ | |||
+ | The above clearly suggest that HtrII follows the modular structure. The presence of helical domains are suggested by the hydrophobic (blue) residues, that occur every 7-8 residues. This begins at residues 210 in the sequence (EVMDR), which is similar to the GenBank Analysis | ||
+ | |||
+ | |||
+ | This is further shown by looking at the hydrophicity traces below. Although the consistency of the 7-8 repeat of hydrophobic residue depends on helix turn propensity | ||
+ | * [[Melbourne/Blue Photosensor Background/HtrII Methyl-accepting helicies| HtrII Methyl-accepting helicies ]] | ||
+ | |||
+ | |||
+ | ==== Analysis of ComP motifs ==== | ||
+ | |||
+ | evidence for HAMP domain | ||
+ | |||
+ | [[Melbourne/Blue Photosensor Background/ComP_BLAST| '''ComP BLAST analysis''' ]] | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/ComP HAMP| ComP-HAMP sequence alignment ]] | ||
+ | |||
+ | This is aligned to the same pfam00672 family as HtrII is above. It is likely that the gaps in the ComP alignment are loops. We will account for this in the fusion variants. | ||
+ | transmembrane prediction confers with this as follows | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/ComP TM| ComP TM finder plot ]] | ||
+ | |||
+ | Evidence for existence of kinase domain: | ||
+ | * [[Melbourne/Blue Photosensor Background/ComP Kinase| ComP-Kinase alignment ]] | ||
+ | |||
+ | |||
+ | Evidence for methylated (or accepting) helices: | ||
+ | analysis based on region between HAMP and Kinase domains (between residues KNTILD| and |MFAEIK) | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/ComP Helix Propensity| ComP Helix Propensity alignment]] | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/ComP Turn Propensity| ComP Turn Propensity alignment]] | ||
+ | |||
+ | * [[Melbourne/Blue Photosensor Background/ComP Hydrophobicity| ComP Hydrophobicity alignment]] | ||
+ | |||
+ | Also refer to direct aligment between comP and HtrII helical regions | ||
+ | * [[Melbourne/Blue Photosensor Background/ comparision| ComP / HtrII Comparison of helical regions ]] | ||
+ | |||
+ | |||
+ | ==== Chosen Fusion Sites ==== | ||
+ | |||
+ | Spudich chose fusion sites that were roughly at the start, middle, end of the HAMP domain ... | ||
+ | |||
+ | so along the those lines, since primer synthesis has gotten cheaper, we have chosen the following 7 sites. | ||
+ | However, these are located immediate after the HAMP domain, so as not to disrupt the signaling. Note the '''Bold''' residue overlaps and is lost :) | ||
+ | |||
+ | The next 5 are referenced to after the HAMP domain finishes in both HtrII and ComP. | ||
+ | |||
+ | Construct 1 - position 0 | ||
+ | HtrII | ||
+ | (Q S V R T S || | ||
+ | ComP | ||
+ | ('''V''' L L V S K A) >> ...QSVRTSLLVSKA... | ||
+ | |||
+ | Construct 2 – position 1 | ||
+ | HtrII | ||
+ | (S V R T S L || | ||
+ | ComP | ||
+ | ('''L''' L V S K A Y) >> ...SVRTSLLVSKAY... | ||
+ | |||
+ | Construct 3 – position 2 | ||
+ | HtrII | ||
+ | (V R T S L E || | ||
+ | ComP | ||
+ | ('''L''' V S K A Y T) >> ...VRTSLEVSKAYT... | ||
+ | |||
+ | Construct 4 – position 3 | ||
+ | HtrII | ||
+ | (R T S L E D || | ||
+ | ComP | ||
+ | ('''V''' S K A Y T F) >> ...RTSLEDSKAYTF... | ||
+ | |||
+ | Construct 5 – position 5 | ||
+ | htrII | ||
+ | (S L E D A K || | ||
+ | ComP | ||
+ | ('''K''' A Y T F E V) >> ...SLEDAKAYTFEV... | ||
+ | |||
+ | Construct 6 – position 16 | ||
+ | HtrII | ||
+ | (A E Q A Q K || | ||
+ | ComP | ||
+ | ('''K''' V I F L D K) >> ...AEQAQKVIFLDK... | ||
+ | |||
+ | Construct 7 – position 24 | ||
+ | htrII | ||
+ | (E E I N T E || | ||
+ | ComP | ||
+ | ('''E''' V G P D W N) >> ...EEINTEVGPDWN... | ||
+ | |||
+ | ==== Future Directions ==== | ||
+ | Will try deleting residues between fusion point so as to rotate the kinase domain relative to the HAMP domain to see what effect this has on the chimera function. | ||
+ | |||
+ | |||
[[Image:seq_align.jpg]] | [[Image:seq_align.jpg]] | ||
[[Media:Example.ogg]] | [[Media:Example.ogg]] |
Latest revision as of 13:40, 26 October 2007
<return to top of background> <return to home page>
The background to the design of the blue photosensor is included here. Specifically the design for the chimeric fusion protein that will be the key link in blue light pathway
Contents |
Preliminaries
Tools used
Restriction Site Analysis - [http://tools.neb.com/NEBcutter2/index.php| NEB cutter]
Sequence Translation - [http://au.expasy.org/tools/dna.html| Translate]
Sequence Aligment - [http://www.jalview.org/download.html| JalView] These were done via known domain databases from GenBank, with a ClustalW Realignment option in the Web Services menu of JalView
- Clustal Color Scheme
- Hydrophobicity Color Scheme
- Helix Propensity Color Scheme
- Turn Propensity Color Scheme
PCR primer design - [http://www.premierbiosoft.com/netprimer/netprlaunch/netprlaunch.html| NetPrimer]
Transmembrane Prediction - [http://www.sbc.su.se/~miklos/DAS/| DAS Transmembrane Prediction]
JalView File of Seq. Alignments - doesn't work ATM
Sequences and Restriction Sites
SopII (sensory rhodopsin II)
DNA, AA, [http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank]
- No IGEM restriction sites
- HaeII (@168) present
HtrII (sensory rhodopsin II transducer)
DNA, AA, [http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3702851&ordinalpos=1&itool=EntrezSystem2.PEntrez.Gene.Gene_ResultsPanel.Gene_RVDocSum genbank]
- No IGEM restriction sites
- No useful restriction site
SopII/HtrII fusion
DNA, AA (frame 2 in Translate - only SopII + HtrII + Linker included in link), linker = TSASA SNGASA,
[http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank]
- No IGEM restriction sites
- Use site from SopII (this is the one that will be used)
ComP (two-component sensor histidine kinase)
DNA (includes IGEM forward and reverse primers (VF2 + VR) and IGEM prefix and suffix, AA, [http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank]
SpeI (@927) deleted HaeII (@1902) inserted
ComA (sensory rhodopsin II transducer)
DNA, AA, [http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=search&term=sopII genbank]
SpeI (@12) deleted HaeII (@433) inserted
Chimera Design
Overview
Chimera will be constructed using a PCR based stitching approach as described by Spudich, (refer to reference)
Analysis of SopII motifs
transmembrane photoreceptor, requires all-trans retinal as substrate... linked to HtrII insert TM analysis here. reference the three papers cited in background
This shows consistent TM helicies throughout the whole sequence
Analysis of HtrII motifs
Methyl-accepting chemotaxis proteins (MCP) are hypothesized to be modular in structure (ref needed). This modularity and homology between most MCPs is evidence by the clear separation of HAMP domains from methyl-accepting helical domains and the sensor kinases. Below is shown evidence for this in HtrII.
This hisitidine kinase also has a clear TM region, from residues 0-80
Genbank mentions the HAMP domain (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases)
This is the key to the propagation of the excitation signal according to (ref needed)
Evidence for the HAMP domain is contained in the following sequence alignment with known HAMP domains from GenBank
This alignment suggest homogoly from residue 65 to 134 in the HtrII sequence. This conforms with the GenBank analysis shown below.
Evidence for methyl-accepting chemo-taxis like domain (these are the likely helices (hydrophobic residue every 7 AA, after the HAMP domain))
The above clearly suggest that HtrII follows the modular structure. The presence of helical domains are suggested by the hydrophobic (blue) residues, that occur every 7-8 residues. This begins at residues 210 in the sequence (EVMDR), which is similar to the GenBank Analysis
This is further shown by looking at the hydrophicity traces below. Although the consistency of the 7-8 repeat of hydrophobic residue depends on helix turn propensity
Analysis of ComP motifs
evidence for HAMP domain
This is aligned to the same pfam00672 family as HtrII is above. It is likely that the gaps in the ComP alignment are loops. We will account for this in the fusion variants. transmembrane prediction confers with this as follows
Evidence for existence of kinase domain:
Evidence for methylated (or accepting) helices:
analysis based on region between HAMP and Kinase domains (between residues KNTILD| and |MFAEIK)
Also refer to direct aligment between comP and HtrII helical regions
Chosen Fusion Sites
Spudich chose fusion sites that were roughly at the start, middle, end of the HAMP domain ...
so along the those lines, since primer synthesis has gotten cheaper, we have chosen the following 7 sites. However, these are located immediate after the HAMP domain, so as not to disrupt the signaling. Note the Bold residue overlaps and is lost :)
The next 5 are referenced to after the HAMP domain finishes in both HtrII and ComP.
Construct 1 - position 0 HtrII (Q S V R T S || ComP (V L L V S K A) >> ...QSVRTSLLVSKA...
Construct 2 – position 1 HtrII (S V R T S L || ComP (L L V S K A Y) >> ...SVRTSLLVSKAY...
Construct 3 – position 2 HtrII (V R T S L E || ComP (L V S K A Y T) >> ...VRTSLEVSKAYT...
Construct 4 – position 3 HtrII (R T S L E D || ComP (V S K A Y T F) >> ...RTSLEDSKAYTF...
Construct 5 – position 5 htrII (S L E D A K || ComP (K A Y T F E V) >> ...SLEDAKAYTFEV...
Construct 6 – position 16 HtrII (A E Q A Q K || ComP (K V I F L D K) >> ...AEQAQKVIFLDK...
Construct 7 – position 24 htrII (E E I N T E || ComP (E V G P D W N) >> ...EEINTEVGPDWN...
Future Directions
Will try deleting residues between fusion point so as to rotate the kinase domain relative to the HAMP domain to see what effect this has on the chimera function.
File:Seq align.jpg Media:Example.ogg