IGEM:Harvard/2006/Adaptamers/Notebook

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Week 4

7/7

Adaptamers:

We've received the short DNA sequences that we'll be using. We are waiting for purified streptavidin protein to come in. The main question is what we will use in our gel shift assay. We cannot use 32P, so our alternatives are:

Invitrogen EMSA kit (cat. E33075) $224. enough for 10 minigel assays.

Roche DIG gel shift (cat. 03353591910) $453. enough for 20 labeling rxns, 200 gel shift rxns, 20 blots, and 20 control rxns. Don't know what 'gel shift reactions' are. Also need nylon membranes, DIG wash and buffer set.

LightShift Chemiluminescent EMSA Kit (prod. # 20148) $349. Enough for 100 binding reactions (??), detection reagants for 800cm^2 membrane.

The first kit uses fluorescent dyes. We would need to buy a $600 filter for the gel imager to use it. The second two involve blotting membranes. Since this project will probably involve trying out a few types of aptamer sequences and many types of intermediate sequences between the two aptamer ends, the latter two, while supposedly more reliable, will likely be too costly. Licor also has a system based on fluorescent dyes but it looks like you buy the parts separately...

Alain suggested that all adaptamers that we create have a sequence that can bind a complementary short sequence; we'd order a lot of labeled short complementary sequence. Sounds like a good idea, as long as those short sequences do not interfere with the aptamer binding.

Week 5

7/11

Shawn and William suggested that for an initial assay, it'd be easy to just stain protein with Coomassie blue. So that's what we attempted.

We ran two 10-20% native polyacrylamide gels at 15 V overnight; the first used some lanes from the Nano group's gel. Visualization to come tomorrow.

The composition of what we added to each line is below; materials were added and incubated for 30 minutes in 2 uL total volume for lanes 1-11, 1-12 prior to dilution to 10 uL including addition of loading dye. Lanes 2-1 to 2-9 were incubated for an hour; longer incubation carried out since DNA basepairing reactions for lanes 2-10 to 2-12 were carried out for 30 minutes using results from 30-minute incubations of lanes 2-1 to 2-9. This incubation time should not be significant.

Materials used: Thrombin: a 2 uM solution of Thrombin. Streptavidin: a 2 uM solution of Streptavidin. Thromb5, Thromb20, Thromb35, Thromb50, Strep5, Strep20, Strep35, Strep50 are described in Plan section above. Bock's buffer is a reaction buffer for DNA-protein binding, used in several papers (see Nano group's page). 10X dye is a few flakes of bromophenol blue + 500 uL Bock's + 500 uL glycerol.

All quantities in uL.

Lane solutions

	1-11	1-12	2-1	2-2	2-3	2-4	2-5	2-6	2-7	2-8	2-9	2-10	2-11	2-12
Thrombin	.5	.5	.5	1	1	1
Streptavidin							.5	.5	1	1	1
Thromb5		1	1
Thromb20				2
Thromb35					2
Thromb50						2
Strep5								2
Strep20									2
Strep35										2
Strep50											2
4X Bock's Buffer (see Nanostructure page)	.5	.5	.5	1	1	1	.5	.5	1	1	1
H2O	1						1
2-2 solution												2
2-3 solution													2
2-4 solution														2
2-7												2
2-8													2
2-9														2
Bock's 1X buffer	7	7	7	7	7	7	7	7	7	7	7	5	5	5
10X dye	1	1	1	1	1	1	1	1	1	1	1	1	1	1

Ran 2 10-20% polyacrylamide gels along with nano group.

7/12

The gels came out completely blank. Bummer. Potential problems were protein concentration, pH of reaction buffer, and voltage. Different concentrations were tried out by the nanogroup to no success.

Update: The machines were never turned on. Double-bummer.

7/13

For now, we will

1) debug SDS-PAGE with the nanos. 2) Search for possible cell surface protein targets for which aptamers have been developed (and have published sequences).

We heard back from the group that had created Lipopolysaccharide aptamers (that cand bind the E. coli cell surface). The group only created a polyclonal batch and never got specific aptamers sequenced before funding was cut. Unfortunate.

Nanos have gotten protein to show up on a gel; they ran it for 15 minutes at 120 V.

7/14

7/12 experiment essentially repeated. Alain kindly imaged the gels; results are shown in Week 5 presentation slides.

Week 6

7/17

Attempted to stain gels from 7/14 with EtBr. Gels were completely blank. The nanostructure group has since confirmed that staining with EtBr following staining with Coomassie Blue does not work.

7/18

Ran a gel with multiple lanes of the same condition in order to have separate visualizations of DNA and protein.

Lanes are as follow:

2: BSA

3: thrombin in BSA

4: thrombin + T5

5: streptavidin

6: streptavidin + S5

7: streptavidin + biotinylated oligos

8: 1 kb ladder

9: 5S

10: 5S + strep

11: 5T

12: 5T + thromb

Where combinations are noted, 4 picomoles DNA + 2 picomoles protein were incubated for 30 minutes in a total reaction volume of 4 uL. Following incubations, solutions were diluted to 10uL including loading dye and run on a 12% polyacrylamide gel at 120 V for 1.5 hours.

Lanes 1-7 were stained with Coomassie Blue; lanes 8-12 with EtBr.

The lane with BSA clearly showed three bands, disagreeing with the results of the Nanostructure group, which suggested that only the bottom-most band belonged to BSA, and the others to thrombin. It was hoped that we had simply added thrombin to the BSA lane, but results from 7/21 showed that BSA in fact was responsible for all the bands.

No shift was observed for thrombin, although both DNA and aptamer bands appeared darker in lanes where they were incubated together, which is inconsistent with binding. Streptavidin only showed very lightly and not at all in the lane with biotin; perhaps streptavidin did bind biotin.

One curiosity is the bands stained with EtBr. S5 is more than double the length of T5, yet they appeared to migrate to the same location. I initially thought that the band somehow matched with the loading dye, but visual inspection showed that this was not the case.

7/21

Following continued negative results obtained by the nanostructure group, we repeated most of 7/18's gel at extremely high concentrations with more attention to the positive control of streptavidin and biotin binding. The rationale was that if binding did not occur at these concentrations, then there was something quite wrong with either our materials or procedure. Aiding our confidence in this experiment, more highly-purified samples of the longer aptamers arrived this week (in particular, S5). Incubations were done in total volumes of 9uL.

1: SeeBlue Plus 2 ladder

2: BSA

3: thrombin (100 pmol)

4: thrombin (100 pmol) + T5 (200 pmol)

5: streptavidin (94.5 pmol)

6: streptavidin (94.5 pmol) + S5 (200 pmol)

7: streptavidin (94.5 pmol) + biotinylated oligos (200 pmol)

8: 1kb dna ladder

9: biotinylated oligos (200 pmol)

10: biotinylated oligos (200 pmol) + streptavidin (94.5 pmol)

11: S5 (200 pmol)

12: S5 (200 pmol) + streptavidin (94.5 pmol)

We finally saw clear bands in all conditions. Unfortunately, BSA was responsible for the primary bands of lanes with thrombin. The smear for thrombin may be due to thrombin glycosylation. Because the fuzzy signal, it is difficult to tell if there is a shift when T5 is added to thrombin. Streptavidin does not appear to be binding S5. The fuzzy signal may be due to excessive protein concentrations; we shall try everything again at 40 pmol DNA + 20 pmol protein.

This time around, we could see new bands for S5. So what's the band consistent across the DNA lanes?

Lower concentration gel

We reconstituted Bovine thrombin in PBS this time around. Lanes are as follows:

Protein

1: SeeBlue Plus 2 ladder

2: thrombin (20 pmol)

3: thrombin (20 pmol) + T5 (40 pmol)

4: streptavidin (20 pmol)

5: streptavidin (20 pmol) + S5 (40 pmol)

6: streptavidin (20 pmol) + biotinylated oligos (40 pmol)

7: 1kb dna ladder

8: nothing + dye

9: T5 (40 pmol)

10: T5 (40 pmol) + thrombin (20 pmol)

11: S5 (40 pmol)

12: S5 (40 pmol) + streptavidin (20 pmol)

Conclusions:

1) Weird DNA band is not due to dye.

2) streptavidin-thrombin binding not detected.

3) Thrombin binding not detected.

Next: Primary: 1) Denature DNA before incubation.

2) Use human thrombin instead of bovine thrombin. 85% homology isn't enough.

Contingency plan: 1) Try a more sensitive binding assay.

2) Try S0, T0 instead of S5, T5

3) Try human thrombin.

4) Run a gel a shorter time to see if T5, biotinylated oligos are resolved separately from mystery band.

Week 7

7/24

This time around, we're denaturing the aptamers before incubating with protein. 5 minutes at 90 degrees followed by 5 minutes at 4 degrees. Unfortunately we haven't gotten human thrombin yet. We'll also try Silver staining, which is supposed to be more sensitive than Coomassie and EtBr.

Protein

1: SeeBlue Plus 2 ladder

2: Benchmark ladder

3: thrombin (20 pmol)

4: thrombin (20 pmol) + T5 (40 pmol)

5: streptavidin (20 pmol)

6: streptavidin (20 pmol) + S5 (40 pmol)

7: streptavidin (20 pmol) + biotinylated oligos (40 pmol)

8: 1kb dna ladder

9: T5 (40 pmol)

10: T5 (40 pmol) + thrombin (20 pmol)

11: S5 (40 pmol)

12: S5 (40 pmol) + streptavidin (20 pmol)

Note: I purposely stained longer than I should because I was determined to see streptavidin. It's there, (lane 7), but it doesn't show up on its own for some reason. The large blotch in the middle of all of this is annoying, too. I'm not sure of its origin. Note for silver stainers: staining for a long time (more than 10 minutes) causes the top and bottom edges of the gels to discolor, possibly making it difficult to resolve bands.

7/25

Low Mass Ladder [invitrogen]: 6 blunt-ended fragments from 100bp to 2000 bp Lambda DNA HindIII (lambda digested by HindIII) [neb]: 23130, 94116, ..., 125 bp

Morning: the big human thrombin experiment.

8% gel run at 120V for 1.5 hours.

lane 1: ladder

lane 2: human thrombin

lane 3: human thrombin + T5

lane 4: human thrombin + denatured T5

lane 5: bovine thrombin

lane 6: bovine thrombin + T5

lane 7: bovine thrombin + denatured T5

lane 8: ladder

lane 9: T5

lane 10: denatured T5

lane 11: denatured T5+ bovine

lane 12: denatured T5+ human

I also attempted to see if the DNA components of our aptamers were capable of binding each other. Each lane contains 40 pmol of oligo or complex. Ran a 12% gel for 1 hour at 120V. Incubation was for 15 minutes total. Denaturation: oligos mixed, heated to 90 C for 5 minutes, then rapidly cooled to 4 C for 5 minutes, followed by 5 minutes at room temperature.

Lane 1: ladder

Lane 2: T20

Lane 3: S20

Lane 4: T20 + S20

Lane 5: T20 + S20; denatured during incubation

Lane 6: T35

Lane 7: S35

Lane 8: T35+S35

Lane 9: T35 + S35; denatured during incubation

Lane 10: T50

Lane 11: S50

Lane 12: T50 + S50 (denaturation condition)

The complementary sections appeared to have come together at a pretty high rate, both for denaturing and non-denaturing conditions.

7/26

Human thrombin info:

T6884-1KU 035K7580

[Link to product info page (includes information sheet)]

1670 NIH units; 3093 NIH units/mg

In light of yesterday's disappointing results, today was an information gathering day. We got in contact with David Liu, who developed the streptavidin aptamer. He and his grad student, Thomas Snyder, have not tried gel shift assays and believe that other methods such as binding the proteins to a nitrocellulose membrane or using a Biacore are more reliable.

We also tried out mfold to determine the secondary structure of our aptamers. The streptavidin aptamers leave the binding region secondary structure intact. However, the thrombin aptamers bind to themselves in the binding region, which could have well explained the lack of binding we observed. Nevertheless, such problems should have been solved by denaturation. Images to come.

7/27

We now have three assays to try:

1) millipore nitrocellulose membranes

The protocol is described [|here]. We may learn how to use this from the good people of Liu lab.

2) Biacore 3000 at the Bauer Center for Genomics

A complex piece of machinery is able to detect how well substrates are binding to a surface (to which the protein in question is bound). We spoke to Clair Reardon of the Bauer Center today; she will soon send us information about using it.

3) Streptavidin beads

Happily, the DNA aptamers to streptavidin were developed to bind streptavidin conjugated to agarose beads. The hope is that we add aptamer, wash, elute, and hopefully we will see aptamer. Hopefully.

We tried adding thrombin to a protein membrane and seeing if we can visualize DNA with EtBr. The answer is.. no. Well sort of.

Dots are just above where I added solution.

First 3 rows of dots have thrombin added to them; last row is blanks

DNA was added to all dots. For rows 1,2,4: T5 added to column 1, 2, 3; S5 added to column 4, 5. For row 3, T20+S20 added except for column 1, where T5 was added. (this was a pretty informalexperiment)

Trans-UV

UV filtered into white light:

Epiwhite:

Although there are slightly lighter spots under the transUV in the first few lanes, there is no distinction for the type of aptamer which is added. Furthermore, the UV light might just be highlighting certain areas that had more solution added to them instead of EtBr. Regardless, you can't see much.

In light of the secondary structure complications of the thrombin aptamer, I mixed together T20 and S20 to see if the complex, which no longer has the unfortunate binding site concealment, could bind to thrombin.

Lane 1: ladder

Lane 2: T20

Lane 3: T20 + thrombin

Lane 4: S20

Lane 5: S20 + thrombin

Lane 6: T20+S20

Lane 7: T20+S20+ thrombin

Oddly enough, we saw no gel shift for T20+S20, which we should have seen as demonstrated previously. While it is unclear that our adaptamer had actually formed, what is clear is that thrombin remained unbound.

Week 8

7/31

Ran pure thrombin aptamer sequence in a gel along with some friends for one hour. Results below.

Lanes:

1: protein ladder

2: thrombin

3: thrombin + T0

4: thrombin + T5

5: thrombin + T35+S35

6: DNA ladder

7: T0

8: T0 + thrombin

9: T5

10: T5 + thrombin

11: T35+S35

12: T35+S35 + thrombin

Protein: 20 pmol; DNA: 40 pmol. T35+S35 incubation: 30 minutes before addition of thrombin. 12% Polyacrylamide gel run for 1 hour at 120V.

Protein:

DNA:

If you compare lanes 2 with 5 and 11 with 12, you will notice a gel shift. If you were here, you'd notice me doing a little dance. :) :) :)

I should curb my enthusiasm a bit and note that the major thrombin band did not shift. Alain suggested that this might be a reason that papers tend to label the DNA, not the protein.

T35+S35 must be heavy enough to not run too far away while the aptamer region is coming off thrombin, unlike T0 (the pure thrombin aptamer). Running the gel for 1 hour may have made a difference, too. Maybe we'll see an even better shift using T50+S50.

8/1

Streptavidin beads have arrived. Product details below:

http://www.sigmaaldrich.com/catalog/search/ProductDetail/FLUKA/85881

A first experiment will just examine the effects of incubating different amounts of thrombin aptamer with the beads.

The beads are supplied at 1.2 ug/uL = 22.6 pmol/uL. Suggested amount per reaction: 25 uL or 566 pmol streptavidin. Amount of DNA added: 10 pmol, 20 pmol, 40 pmol, 80 pmol, 160 pmol, 320 pmol. Assuming capture of all DNA, if 1% of the DNA is in a solution in the last two cases, we should still be able to visualize it.

Beads were first washed 3X and transferred to equal volume of Bittker binding buffer (Bittker 2002; see [| stock solutions page]). Total bead/DNA reaction volume was 50 uL. Beads were shook for 30 minutes, then washed 3X in 25 uL Bittker buffer. Washes were collected. DNA attached to beads was eluted by shaking with 25 uL 50% wt/v streptavidin for 30 minutes followed by 25 uL Bittker buffer. 18 uL of wash and buffer solutions were then run on a 12 % polyacrylamide gel for 1 hour then stained with EtBr.

Lane 1: 1000 kb+ ladder

Lane 2: S5

Lane 5: 10 pmol S5 wash

Lane 6: 10 pmol S5 elution

Lane 7: 20 pmol S5 wash

Lane 8: 20 pmol S5 elution

Lane 9: 40 pmol S5 wash

Lane 10: 40 pmol S5 elution

Lane 11: 80 pmol S5 wash

Lane 12: 80 pmol S5 elution

Lane 1: 1000 kb+ ladder

Lane 2: S5

Lane 3: 160 pmol S5 wash

Lane 4: 160 pmol S5 elution

Lane 5: 320 pmol S5 wash

Lane 6: 320 pmol S5 elution

Lane 7: 500 pmol miniprep (nonspecific dna) wash

Lane 8: 500 pmol miniprep (nonspecific dna) elution

Lane 9: 320 pmol S5 wash (incubation with thrombin beads)

Lane 10: 320 pmol S5 elution (incubation with thrombin beads)

Several things were done wrong here:

Wash volumes were too small so lots of extra DNA was found in the elution. Incubated with miniprep dna to test non-specific DNA interaction. These didn't migrate very far. Used way too many thrombin beads. That control should have been for how much agarose S5 is binding rather than how much of a different time of protein it is binding.

Nonetheless, the miniprep DNA elution fraction seemed to have less DNA in it than elutions of other lanes with S5 and less DNA, which is somewhat promising.

8/2

MANY EDITS TO COME.. JUST UPLOADING FILES.

Two more gels:

Adaptamer-35 extravaganza:

1: SeeBlue Plus 2 ladder

2: thrombin

3: thrombin + T35

4: thrombin + S35

5: thrombin + T35 + S35

6: DNA ladder

7: T35

8: T35 + thrombin

9: S35

10: S35 + thrombin

11: S35 + T35

12: S35 + T35 + thrombin

Protein:

DNA:

Adaptamer-50 extravaganza:

1: SeeBlue Plus 2 ladder

2: thrombin

3: thrombin + T50

4: thrombin + S50

5: thrombin + T50 + S50

6: DNA ladder

7: T50

8: T50 + thrombin

9: S50

10: S50 + thrombin

11: S50 + T50

12: S50 + T50 + thrombin

Protein: File:Cst801adapt50prot.jpg

DNA:

8/5

4 more gels

a35 done on 6% gel retardation gel a20 done on 12% Tris-glycine gel

a35 +thromb

a35 + strep

a20 +thromb

a20 + strep

8/6

Week 9

8/7

Finished up new adaptamer design. The program I used to aid the process will be posted shortly. See oligos page for sequences.

8/8

Experiments:

1) Speed Vac

2) thrombin beads

• 1.Speed Vac

Take remaining fraction of 8/6 elutions (theoretically 144 of 152 uL) and concentrate using the speed vac, then run on gel and stain with SYBR gold.

S0: streptavidin aptamer (40 bp single stranded) SB: streptavidin beads TB: thrombin beads

1: ladder

2: 20 pmol S0

3: 10 uL SB + 40 pmol S0

4: 25 uL SB + 40 pmol S0

5: 50 uL SB + 40 pmol S0

6: 100 uL SB + 40 pmol S0

7: 150 uL SB + 40 pmol S0

8: T35 (50bp, single stranded oligo)

9: 150uL TB + 40 pmol S0

The bands are a bit brighter, now (same imager settings). The 100uL sample has very little in it: enough beads were in this sample so that they precipitated following concentration and it was only possible to add a tiny bit of fluid.

• 2.Thrombin Beads

Repeat 8/6 experiment with thrombin beads. Slightly higher concentration of T0 will be used. Thrombin concentration (of beads) is unclear, but we'll just try different volumes.

Both gels are 4-20% polyacrylamide gels run in TBE for 50 minutes.

S0: streptavidin aptamer (40 bp single stranded) SB: streptavidin beads TB: thrombin beads

1: ladder

3: 20 pmol T0

4: 10 uL TB + 80 pmol T0

5: 25 uL TB + 80 pmol T0

6: 50 uL TB + 80 pmol T0

7: 100 uL TB + 80 pmol T0

8: 150 uL TB + 80 pmol T0

9: S5 (55bp, single stranded oligo)

10: 150uL SB + 80 pmol T0

1: ladder

2: 20 pmol T0

3: 10 uL TB + 80 pmol T0

4: 25 uL TB + 80 pmol T0

5: 50 uL TB + 80 pmol T0

6: 100 uL TB + 80 pmol T0

7: 150 uL TB + 80 pmol T0

8: S5 (55bp, single stranded oligo)

9: 150uL SB + 80 pmol T0

8/9

• The A20 experiment

Question: Is A20.1 able to bind both of its targets at once?

Setup: We will add a constant amount of A20 to a constant volume of streptavidin beads, then incubate with varying amounts of thrombin. After a few washes, we will elute whatever is bound to the beads with free streptavidin. Controls will be replacement of A20 with S20 or T20 (nonspecific interaction of thrombin with DNA for former, binding of thrombin to beads via T20 alone in latter) and replacement of streptavidin beads with trypsin beads (testing binding to agarose).

Specific setup: A20 was prepared by mixing equal molar solutions of S20 and T20, heating to 95 C and cooling slowly to room temperature for 20 minutes. Streptavidin beads were washed three times with Bittker buffer and resuspended in an equal volume of Bittker buffer. 100 uL streptavidin or trypsin beads were combined with 160 pmol A20, S20, or T20 to a total volume of 120 uL and incubated for 30 minutes on a shaker. Varying concentrations of thrombin were added and shook for 30 minutes more. Solutions were then washed three times in Bittker buffer; first wash was collected. Bound substrates were then eluted by incubating with 100 uL 50% w/v streptavidin for 1 hour on a shaker. Solutions were then centrifuged and elutions collected. 8 uL of solutions + 2uL 5X TBE Hi Density Loading Buffer were loaded onto 4-20% pre-cast polyacrylamide gels in TBE buffer and run for 30 minutes. 9 uL solutions + 1 uL 10X Tris-glycine loading buffer were run on 12% pre-cast polyacrylamide gels in Tris-glycine buffer. Duplicate samples of washes and elutions were stained with either Coomassie blue or Ethidium Bromide.

Ideal results:

Protein:

Elutions: Increasing Coomassie staining as the concentration of thrombin increases; no thrombin in any control lane.

Washes: Decreasing Coomassie staining as the concentration of thrombin increases; strong bands in control lanes.

DNA:

Elutions: Greater intensity for lanes with A20, S20

Washes: Greater intensity for lanes with T20, trypsin beads.

Background: From the past experiments with thrombin and streptavidin beads, we know that following a wash, more S0 remains on streptavidin beads than T0 on thrombin beads when the same concentrations of aptamer and streptavidin is used. A number of factors may have contributed to this observation, among them the fact that bovine rather than human thrombin is conjugated to the agarose. Therefore we will use streptavidin rather than thrombin beads as a base. Using either type of beads, a large fraction of even pure aptamer is lost during the wash; therefore it make sense to try rather large amounts of beads, adaptamer, and thrombin concentrations.

Results:

Conditions labeled as follows:

SB: streptavidin beads TrB: trypsin beads

1: 100 uL SB + 160 pmol A20 + 40 pmol thrombin 2: 100 uL SB + 160 pmol A20 + 80 pmol thrombin 3: 100 uL SB + 160 pmol A20 + 160 pmol thrombin 4: 100 uL SB + 160 pmol A20 + 320 pmol thrombin 5: 100 uL SB + 160 pmol T20 + 320 pmol thrombin 6: 100 uL SB + 160 pmol S20 + 320 pmol thrombin 7: 100 uL TB + 160 pmol A20 + 320 pmol thrombin

DNA lanes

Lane	Condition
1	10bp ladder
2	20 pmol T20
3	20 pmol S20
4	20 pmol A20
5	1
6	2
7	3
8	4
9	5
10	6
11	7

Washes

Elutions

Protein lanes

Lane	Condition
1	10bp ladder
2
3	40 pmol thrombin
4	1
5	2
6	3
7	4
8	5
9	6
10	7

Washes

Elutions

Results:

A20 binds well to streptavidin. Whether thrombin does is still up to question. The streptavidin found in the elution makes it difficult to detect trace amounts of thrombin (and hopefully there is some). However, we'll take advantage of the fact that silver staining does not stain streptavidin well in another attempt to detect thrombin tomorrow.

8/10

Destained yesterday's protein elution gel and Silver stained it; see 8/9 for lanes.

There was so much streptavidin that it actually was stained this time. No thrombin was really detectable in any lane.

8/11

Magnetic beads came today.

• Bead assay

We will try to detect the linkage of streptavidin and thrombin beads. The linkage should be visible since the streptavidin beads are a murky brown and the agarose thrombin beads are translucent white. The problem is concentrations of proteins: while the agarose beads have a binding capacity of 15-30 ug biotin/mL [| (link)], the magnetic beads have a capacity of 1 ng/mL, a seemingly bizarre difference. As a secondary assay, we'll attempt to detect whatever is linked to the streptavidin beads by cleaving with Proteinase K. This should hopefully cleave thrombin and be visible on the gel. Unfortunately this will still have the problem from the 8/9 assay of interference with cleaved streptavidin bands.

400 uL magnetic strepavidin beads were concentrated to 4X in Bittker Buffer and 400 pmol A50 or S0 were added to a total volume of 140 uL. Beads and DNA were incubated for 30 minutes. 150 uL thrombin beads (washed and resuspended in Bittker Buffer) were added and solution was incubated for another hour. Magnet was then applied as shown below.

Results:

In both conditions, thrombin beads came intertwined with streptavidin beads, making their separation impossible. A50 seemed to take longer to float to the magnet, which hopefully is related to it having bulkier particles, but certainly there is nothing conclusive.

• 8/9 experiment one more time..

The band where thrombin should be in the Silver staining experiment is pretty unclear thanks to streptavidin staining. I decided to try denaturing the proteins in hopes of seeing more distinct bands.

12% SDS PAGE gel:

Many of the lanes have bands that are unaccounted for by both streptavidin and thrombin. Since the streptavidin bands from previous native gels are consistent with the bands seen in the 8/9 native gels, these are likely streptavidin. Perhaps some of the sample was lost while denaturing it.

8/12

Attracting streptavidin magnetic beads with the 8/9 setup doesn't seem to work well: attraction to the side makes it difficult to discern a difference between setups. Orienting the magnet vertically seems a little more promising since it is the strength of the magnet directly against gravity; hopefully the gradients of magnetic particles will differ based on differing properties of large aggregates (densities, magnetic bead: thrombin bead ratio, surface area (and friction) differ. The vertical setup yields very little pulling power even for .2 mL PCR tubes, so I cut a couple up to get the magnet in range. This experiment is questionable as I reused the refrigerated 8/10 experiment beads (incubating on a rocker for 30 minutes).

I also reran streptavidin plus the various types of thrombin we've used and BSA on a SDS-PAGE 12% Tris-Glycine gel for 1.5 hours. Results shown below.

Lane	Condition
1	Seeblue plus2 ladder
2	8 uL 1% BSA
3	40 pmol Haematologic Technonlogies human alpha thrombin
4	40 pmol Sigma Human thrombin
5	40 pmol Bovine Thrombin w/o BSA
6	90 pmol streptavidin