Haynes:TypeIIS Assembly

From OpenWetWare

(Difference between revisions)
Jump to: navigation, search
(14 intermediate revisions not shown.)
Line 12: Line 12:
-
'''Use PCR to prepare the parts'''
+
{| width=800px cellpadding=5
 +
|- valign="top"
 +
| <font size=3>'''Use PCR to prepare the parts'''</font>
 +
|
* Multiple parts can be assembled in one step.
* Multiple parts can be assembled in one step.
* Parts and the destination vector should be amplified by PCR.
* Parts and the destination vector should be amplified by PCR.
* Make sure that none of the parts/ vector have any BsmBI sites!
* Make sure that none of the parts/ vector have any BsmBI sites!
-
 
-
{| width=800px
 
|-
|-
| [[Image:Haynes_TIIS_fig1.png|250px|Figure 1]] || First, map out your assembly. In this example, three parts, A, B, and C will be assembled and inserted into a Vector.
| [[Image:Haynes_TIIS_fig1.png|250px|Figure 1]] || First, map out your assembly. In this example, three parts, A, B, and C will be assembled and inserted into a Vector.
Line 46: Line 47:
Note: For insertion into pSB1A3, "4 bp of Vector right bottom strand" = <font color=#660099>'''TAGT'''</font>
Note: For insertion into pSB1A3, "4 bp of Vector right bottom strand" = <font color=#660099>'''TAGT'''</font>
<br>
<br>
-
|-
+
|- valign="top"
-
| image || Run separate 50 μL PCR reactions for each part. If you are using plasmid DNA as a template, use no more than 10 ng in order to minimize carry-over into the final bactial transformation step. Check 10 μL of the reaction on and agarose gel. Purify the remaining 40 μL of PCR products using a Zymo clean and Concentrator kit (or similar PCR clean up kit).
+
| [[Image:Haynes_TIIS_fig6.png|250px|Figure 6]] || Run separate 50 μL PCR reactions for each part. If you are using plasmid DNA as a template, use no more than 10 ng in order to minimize carry-over into the final bacterial transformation step. Check 10 μL of the reaction on and agarose gel. Purify the remaining 40 μL of PCR products using a Zymo clean and Concentrator kit (or similar PCR clean up kit).
-
|}
+
-
'''Digestion/ Ligation Reaction'''
 
-
1. Dilute the purified PCR product to 20 fmol/μL
+
|- valign="top"
 +
| <br><font size=3>'''Digestion/ ligation reaction'''</font>
 +
| <br>'''Dilute the purified PCR product to 20 fmol/μL'''
* Measure ng/μL of the purified sample.
* Measure ng/μL of the purified sample.
-
* Use the following formula to calculate the volume of purified DNA (x) you will need to dilute in a final volume of 20 μL
+
* The volume of purified DNA (x) you will need to dilute in a final volume of 20 μL = 20 μL final volume * 20 fmols/μL * '''length in bp''' * 650 fg/fmol ÷ 1,000,000 fg/ng  ÷ '''measured ng/μL'''
-
** x = '''20''' μL final volume * '''20''' fmols/μL * '''length in bp''' * '''650''' fg/fmol ÷ '''1,000,000''' fg/ng  ÷ '''measured ng/μL'''
+
** Formula: x = '''length in bp''' ÷ '''measured ng/μL''' * 0.26
-
** '''Formula: length in bp ÷ measured ng/μL * 0.26'''
+
|-
-
 
+
| [[Image:Haynes_TIIS_fig7.png|250px|Figure 7]]
-
 
+
| '''Perform BsmBI/ T4 ligase mediated assembly'''
-
2. Golden Gate Reaction
+
* BsmBI cuts the DNA fragments and creates complementary overhangs.
-
 
+
* Complementary sticky ends anneal via base pairing.
 +
* T4 ligase seals gaps in the phosphodiester DNA backbone.
{| {{table}}
{| {{table}}
|-  
|-  
| bgcolor="grey" | Reagent
| bgcolor="grey" | Reagent
| bgcolor="grey" | Vol.
| bgcolor="grey" | Vol.
 +
| rowspan=7 | '''Thermal cycling'''
 +
* [45°C, 2 min.; 16°C 5 min.] x25
 +
* 60°C, 10 min.
 +
* 80°C, 20 min.
 +
* 4°C, ∞
|-
|-
| 20 fmol of each DNA part || up to 8.0
| 20 fmol of each DNA part || up to 8.0
Line 79: Line 86:
|}
|}
-
Thermal cycling
+
|}
-
* [45°C, 2 min.; 16°C 5 min.] x25
+
-
* 60°C, 10 min.
+
-
* 80°C, 20 min.
+
-
* 4°C, ∞
+
-
3. Transformation
+
<font size=3>'''Bacterial transformation'''</font>
* Add total volume (10.0 μL) to 50 μL chemically competent cells  (e.g., BL21) in a 2.0 mL tube.
* Add total volume (10.0 μL) to 50 μL chemically competent cells  (e.g., BL21) in a 2.0 mL tube.
* Incubate on ice for 2 min., heat shock at 42°C for exactly 90 sec., immediately place on ice.
* Incubate on ice for 2 min., heat shock at 42°C for exactly 90 sec., immediately place on ice.

Revision as of 21:32, 19 January 2013

<- Back to Protocols

Type IIS Assembly

by Karmella Haynes, 2013


Principle: The familiar "BioBrick cloning" enzymes (i.e., EcoRI, NotI, XbaI, SpeI, PstI) are Type II restriction enzymes, which cut the sequences that they specifically bind to. The Type IIS Assembly method uses a Type IIS restriction enzyme, which binds at a specific sequence and cuts at a non-specific location exactly five base pairs away. As a result, the enzyme cleaves away its own binding site and leaves behind the most useful feature of assembly, sticky overhangs. When designed properly, Type IIS sites can be used to perform seamless assembly of parts. As an added convenience, this protocol allows cutting and ligation to occur in a single tube, as a single reaction. Thus, gel purification steps can be eliminated.

This protocol uses the Type IIS restriction enzyme BsmBI (CGTCTCn/nnnn).


Use PCR to prepare the parts
  • Multiple parts can be assembled in one step.
  • Parts and the destination vector should be amplified by PCR.
  • Make sure that none of the parts/ vector have any BsmBI sites!
Figure 1 First, map out your assembly. In this example, three parts, A, B, and C will be assembled and inserted into a Vector.
Figure 2 Design a pair of primers to add BsmBI sites to the ends of a vector backbone. The "cacacca" before BsmBI is used to help restriction enzyme positioning. The "a" after BsmBI is a spacer that is required to generate a correct 4-base sticky end.

Vector Primers

  • Forward Primer: 5'-cacaccaCGTCTCa + 15 bp of "Vector right" top strand
  • Reverse Primer: 5'-cacaccaCGTCTCa + 15 bp of "Vector left" bottom strand

pSB1A3 Vector Primers - already available in the Haynes lab freezer

  • Forward Primer gg0001: 5'-cacaccaCGTCTCaactagtagcggccgct
  • Reverse Primer gg0002: 5'-cacaccaCGTCTCatctagatgcggccgcg


Figure 3 Part A Primers
  • Forward Primer: 5'-cacaccaCGTCTCa + 4 bp of "Vector left" top strand + 15 bp of "Part A" top strand

Note: For insertion into pSB1A3, "4 bp of vector left" = TAGA

  • Reverse Primer: 5'-cacaccaCGTCTCa + 4 bp of "Part B" bottom strand + 15 bp "Part A" bottom strand


Figure 5 Part B Primers
  • Forward Primer: 5'-cacaccaCGTCTCa + 15 bp of "Part B" top strand
  • Reverse Primer: 5'-cacaccaCGTCTCa + 4 bp of "Part C" bottom strand + 15 bp "Part B" bottom strand


Figure 5 Part C Primers
  • Forward Primer: 5'-cacaccaCGTCTCa + 15 bp of "Part C" top strand
  • Reverse Primer: 5'-cacaccaCGTCTCa + 4 bp of "Vector right" bottom strand + 15 bp "Part C" bottom strand

Note: For insertion into pSB1A3, "4 bp of Vector right bottom strand" = TAGT

Figure 6 Run separate 50 μL PCR reactions for each part. If you are using plasmid DNA as a template, use no more than 10 ng in order to minimize carry-over into the final bacterial transformation step. Check 10 μL of the reaction on and agarose gel. Purify the remaining 40 μL of PCR products using a Zymo clean and Concentrator kit (or similar PCR clean up kit).



Digestion/ ligation reaction

Dilute the purified PCR product to 20 fmol/μL
  • Measure ng/μL of the purified sample.
  • The volume of purified DNA (x) you will need to dilute in a final volume of 20 μL = 20 μL final volume * 20 fmols/μL * length in bp * 650 fg/fmol ÷ 1,000,000 fg/ng ÷ measured ng/μL
    • Formula: x = length in bp ÷ measured ng/μL * 0.26
Figure 7 Perform BsmBI/ T4 ligase mediated assembly
  • BsmBI cuts the DNA fragments and creates complementary overhangs.
  • Complementary sticky ends anneal via base pairing.
  • T4 ligase seals gaps in the phosphodiester DNA backbone.
Reagent Vol. Thermal cycling
  • [45°C, 2 min.; 16°C 5 min.] x25
  • 60°C, 10 min.
  • 80°C, 20 min.
  • 4°C, ∞
20 fmol of each DNA part up to 8.0
10x T4 ligase buffer (Promega) 1.0
T4 ligase (NEB) 0.25
BsmBI 0.5
dH2O 0.25
  10.0 μL


Bacterial transformation

  • Add total volume (10.0 μL) to 50 μL chemically competent cells (e.g., BL21) in a 2.0 mL tube.
  • Incubate on ice for 2 min., heat shock at 42°C for exactly 90 sec., immediately place on ice.
  • Add 800 μL sterile SOC medium.
  • Grow with shaking at 37°C for 30 min.
  • Pellet the cells at top speed in a microcentrifuge for 3 min. at room temp.
  • Discard the supernatant. Resuspend the cells in 100 μL LB + antibiotic.
  • Plate cells on pre-warmed LB agar + antibiotic. Grow overnight at 37°C.
    • Quick-transormation (e.g., DH5α-Turbo) is not recommended
Personal tools