Difference between revisions of "Team:UCLA/Notebook/Spider Silk Genetics"

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<details>
 
<details>
 
   <summary>7/26/2015 - 8/1/2015</summary>
 
   <summary>7/26/2015 - 8/1/2015</summary>
 +
  <a href="https://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/29_July_2015"><li>7/29/2015 - Digestion, Transformation of M2-12(T7), M2-15(1C3)</li></a>
 
   <a href="https://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/28_July_2015"><li>7/28/2015 - Maxiprep and BsaI Digestion for M1-AB, BC, CA. Sequencing for M2-12(1C3)</li></a>
 
   <a href="https://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/28_July_2015"><li>7/28/2015 - Maxiprep and BsaI Digestion for M1-AB, BC, CA. Sequencing for M2-12(1C3)</li></a>
 
   <a href="https://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/27_July_2015"><li>7/27/2015 - M2-12(1C3) Colony PCR, M-15 Amplification</li></a>
 
   <a href="https://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/27_July_2015"><li>7/27/2015 - M2-12(1C3) Colony PCR, M-15 Amplification</li></a>

Revision as of 16:28, 3 August 2015

iGEM UCLA




Spider Silk Genetics Notebook

7/26/2015 - 8/1/2015
  • 7/29/2015 - Digestion, Transformation of M2-12(T7), M2-15(1C3)
    •
  • 7/28/2015 - Maxiprep and BsaI Digestion for M1-AB, BC, CA. Sequencing for M2-12(1C3)
    •
  • 7/27/2015 - M2-12(1C3) Colony PCR, M-15 Amplification
    •
  • 7/26/2015 - Transformation of M2-12(1C3) into DH5(alpha)
    •
    7/19/2015 - 7/25/2015
  • 7/24/2015 - PCR amplification for M2-15, Troubleshooting Cloning for M2-12(1C3)
    •
  • 7/23/2015 - ICA for M2-15, Miniprep for M1-AB,BC,CA and M2-12(1C3) for Sequencing
    •
  • 7/22/2015 - BsaI Digestion of M2-SeqAB, Midiprep for M2-AB,BC,CA
    •
  • 7/21/2015 - Cloning M2-12(1C3) and MaSp1 AB, BC, CA
    •
  • 7/20/2015 - Cloning M2-9(T7) and M2-12(1C3), MaSp1 PCR End-Extension
    •
    7/12/2015 - 7/18/2015
  • 7/18/2015 - Sequencing Results for M2-3(T7), M2-6(T7), and M2-9(1C3)
    •
  • 7/17/2015 - Miniprep, and Sequencing for M2-3(T7), M2-6(T7), and M2-9(1C3)
    •
  • 7/16/2015 - ICA for MaSp2 12-mer, Liquid Culture for MaSp2 3-mer(T7), MaSp2 6-mer(T7), and MaSp2 9-mer(pSB1C3)
    •
  • 7/15/2015 - Subcloning MaSp2 3-, 6-mer into T7 expression Vector, Cloning MaSp2 9-mer into pSB1C3
    •
  • 7/14/2015 - ICA 9-mer Again: Electric Boogaloo
    •
  • 7/13/2015 - ICA 6-, 9-mer PCR amplification Temperature Testing
    •
    7/5/2015 - 7/11/2015
  • 7/10/2015 - ICA for 6-mer and 9-mer
    •
  • 7/9/2015 - Ligation and Transformation of 3-mer, 6-mer and MaSp2 Seq AB
    •
  • 7/8/2015 - EcoRI, PstI Digestion of 3-mer, 6-mer, MaSp2 Seq AB, and pSB1C3: Cloning Preparation
    •
  • 7/7/2015 - Assembly of MaSp2 Sequencing Monomer AB, and ICA testing using M-270 Beads
    •
  • 7/6/2015 - Assembly of MaSp2 Sequencing Core, and ICA testing using M-270 Beads
    •
    6/28/2015 - 7/4/2015
  • 7/2/2015 - 6-mer Amplification using Post-elution Primers
    •
  • 7/1/2015 - 6-mer Ligation without beads
    •
    6/21/2015 - 6/27/2015
  • 6/26/2015 - ICA Troubleshooting with reduced initiator
    •
  • 6/25/2015 - ICA Troubleshooting to assess bead amplification
    •
  • 6/24/2015 - ICA Troubleshooting to assess bead binding: results
    •
  • 6/23/2015 - ICA Troubleshooting to assess bead binding
    •
    6/14/2015 - 6/20/2015
  • 6/19/2015 - Initial ICA Testing
    •
  • 6/18/2015 - BsaI Digestion of VF/R Amplified MaSp2
    •
  • 6/17/2015 - PCR amplification of MaSp using VF2, VR
    •
    5/31/2015 - 6/6/2015
  • 6/5/2015 - ICA Oligos Characterization
    •
  • 6/3/2015 - ICA Oligos Characterization
    •
  • 6/2/2015 - Gel purification of BsaI digested MaSp2
    •
  • 6/1/2015 - Preparing to test Initiator, Terminator, and Capping Oligos: PCR amplification and BsaI Digestion
    •
    5/24/2015 - 5/30/2015
  • 5/29/2015 - T7 Ligation Test for VF/R amplified MaSp
    •
  • 5/28/2015 - BsaI Digestion of VF/R amplified MaSp2
    •
  • 5/27/2015 - Temperature Test for VF/R amplification of MaSp, Large-scale amplification of MaSp 2AB, 2BC, 2CA
    •
  • 5/26/2015 - BsaI Digestion of VF/R amplified MaSp2
    •
    5/17/2015 - 5/23/2015
  • 5/22/2015 - PCR amplification of MaSp2 using VF2, VR
    •
  • 5/21/2015 - PCR amplification of MaSp2 using VF2, VR Cycle Testing
    •
  • 5/20/2015 - PCR amplification of MaSp2 using VF2, VR
    •
  • 5/19/2015 - PCR amplification test for MaSp2 plasmid
    •
    5/10/2015 - 5/16/2015
  • 5/13/2015 - NotI Concatemer Ligation
    •
  • 5/12/2015 - T4/T7 Ligation Tests continued
    •
  • 5/11/2015 - BsaI Digestion of MaSp2 Plasmids
    •
    5/3/2015 - 5/9/2015
  • 5/8/2015 - T4/T7 Ligation Test
    •
  • 5/7/2015 - BsaI Digestion of MaSp plasmids
    •
  • 5/6/2015 - DNA Maxiprep
    •
  • 5/5/2015 - DNA Miniprep
    •
  • 5/4/2015 - BsaI Digestion Test
    •
    4/26/2015 - 5/2/2015
  • 5/1/2015 - Primer Exhaustion Calculation
    •
  • 4/30/2015 - Post-elution PCR amplification of MaSp2 plasmids
    •
  • 4/29/2015 - Post-elution PCR amplification of MaSp2 plasmids
    •
  • 4/28/2015 - Post-elution PCR amplification of MaSp2 plasmids
    •
  • 4/27/2015 - Initial ICA Ligation Test
    •
    4/19/2015 - 4/25/2015
  • 4/24/2015 - Sending DNA for sequencing
    •
  • 4/23/2015 - Miniprep DNA for sequencing
    •
  • 4/22/2015 - Colony PCR
    •
  • 4/21/2015 - Ligation of MaSp sequences into pSB1C3 and Transformation
    •
  • 4/20/2015 - PCR amplification of pSB1C3 and EcoRI, PstI digestion
    •
    4/12/2015 - 4/18/2015
  • 4/17/2015 - Amplification of pSB1C3
    •
  • 4/16/2015 - PCA of MaSp2 Pieces
    •
  • 4/15/2015 - PCA of MaSp2 Pieces
    •
  • 4/14/2015 - PCA of MaSp2 Pieces
    •
  • 4/13/2015 - PCA of MaSp2 Pieces
    •

    Goals

    Our goal is to be able to implement Iterative Capped Assmebly (ICA) for use in designing custom spider silk genes. The spider silk protein has a highly repetitive primary structure, and its properties can be changed by changing the sequence and identities of these repeats. We want to be able to fully control the primary sequence of our silk gene, and develop a quick, efficient method of customizing assembly of the spider-silk genes.

    Achievements

    • We started testing ICA on 6/19/2015
    • We successfully constructed biobricks that contain our silk genes and the sticky overhangs. 4/24/2015
    • We proved that our designed sticky ends work as expected, and exhibit specific binding, showing that ICA can work in spider silk genes. 5/8/2015 and 5/12/2015
    • We have established a protocol generating fragments to be used in ICA.
    • We successfully characterized the use of ICA oligos with MaSp AB, BC, CA and showed that they could work in ICA! 6/3/2015
    • We successfully made a 3-mer using the ICA protocol on M-270 Streptavidin Beads! 7/7/2015
    • Find a list of our designed protocols here!

    List of Parts

    • [http://parts.igem.org/Part:BBa_K1763002 MaSp2 AB]
    • [http://parts.igem.org/Part:BBa_K1763003 MaSp2 BC]
    • [http://parts.igem.org/Part:BBa_K1763004 MaSp2 CA]
    • [http://parts.igem.org/Part:BBa_K1763009 MaSp2 Seq-AB]
    • [http://parts.igem.org/Part:BBa_K1763010 MaSp1 AB]
    • [http://parts.igem.org/Part:BBa_K1763011 MaSp1 BC]
    • [http://parts.igem.org/Part:BBa_K1763012 MaSp1 CA]

    What to accomplish next

    • We are working on optimizing PCR amplification of MaSp and BsaI digestion so as to get the most amount of working monomers for ICA.--DONE! see here
    • We need to characterize our MaSp monomers and how they behave when used with the initiators, terminators, and capping oligos that are also used in ICA.--DONE! 6/3/2015
    • We are going to start actual ICA soon.--STARTED! see 6/19/2015
    • We are optimizing ICA to get it to work just right!
    • Our final goal is to make a several different 15-mers that have different rations of MaSp1 and MaSp2 that we can express and characterize.

    Raw lab notebook entries

    April
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    27 28 29 30
    May
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    11 12 13 14 15 16 17
    18 19 20 21 22 23 24
    25 26 27 28 29 30 31
    June
    M T W T F S S
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    8 9 10 11 12 13 14
    15 16 17 18 19 20 21
    22 23 24 25 26 27 28
    29 30
    July
    M T W T F S S
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    27 28 29 30 31
    August
    M T W T F S S
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    10 11 12 13 14 15 16
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    31
    September
    M T W T F S S
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    14 15 16 17 18 19 20
    21 22 23 24 25 26 27
    28 29 30