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==Data==
==Data==
All data are shown with Alanine at 25uM to indicate what "no reaction" looks like.
<u>Alanine</u>
<u>Alanine</u>
{| style="float:right; border:1px solid #BBB;margin:.46em 0 0 .2em"
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Alanine.jpg‎|300px]] [[Image:01112017 AuNP Ala.png‎|300px]]
|}
 
<u>Arginine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Arginine.jpg‎|300px]] [[Image:01112017 AuNP Arg.png‎|300px]]
|}
 
<u>Asparagine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Asparagine.jpg‎|300px]] [[Image:01112017 AuNP Asn.png‎|300px]]
|}
 
<u>Aspartic Acid</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Aspartic Acid.jpg‎|300px]] [[Image:01112017 AuNP Asp.png‎|300px]]
|}
 
Note: I think that aspartic acid is an outlier because it has an N-methyl protecting group instead of an N-acetyl protecting group. My hunch is that Aspartic acid won't make nanoparticles with different N-protection.
 
<u>Cysteine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Cysteine.jpg‎|300px]] [[Image:01112017 AuNP Cys.png‎|300px]]
|}
 
<u>Glutamine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Glutamine.jpg‎|300px]] [[Image:01112017 AuNP Gln.png‎|300px]]
|}
 
<u>Glutamic Acid</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Glutamate.jpg‎|300px]] [[Image:01112017 AuNP Glu.png‎|300px]]
|}
 
<u>Glycine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Glycine.jpg‎|300px]] [[Image:01112017 AuNP Gly.png‎|300px]]
|}
 
<u>Histidine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Histidine.jpg‎|300px]] [[Image:01112017 AuNP His.png‎|300px]]
|}
 
<u>Isoleucine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Isoleucine.jpg‎|300px]] [[Image:01112017 AuNP Ile.png‎|300px]]
|}
 
<u>Leucine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Leucine.jpg‎|300px]] [[Image:01112017 AuNP Leu.png‎|300px]]
|}
 
<u>Lysine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Lysine.jpg‎|300px]] [[Image:01112017 AuNP Lys.png‎|300px]]
|}
 
Note: this data for Nα-acetyl lysine doesn't match with my previous data for lysine. I think that the primary amine on the side chain may also be protected. I need to check into this.
 
<u>Methionine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Methionine.jpg‎|300px]] [[Image:01112017 AuNP Met.png‎|300px]]
|}
 
<u>Phenylalanine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Phenylalanine.jpg‎|300px]] [[Image:01112017 AuNP Phe.png‎|300px]]
|}
 
<u>Proline</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Proline.jpg‎|300px]] [[Image:01112017 AuNP Pro.png‎|300px]]
|}
 
<u>Serine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Serine.jpg‎|300px]] [[Image:01112017 AuNP Ser.png‎|300px]]
|}
 
<u>Threonine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Threonine.jpg‎|300px]] [[Image:01112017 AuNP Thr.png‎|300px]]
|}
 
<u>Tryptophan</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Tryptophan.jpg‎|300px]] [[Image:01112017 AuNP Trp.png‎|300px]]
|}
 
<u>Tyrosine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Tyrosine.jpg‎|300px]] [[Image:01112017 AuNP Tyr.png‎|300px]]
|}
 
<u>Valine</u>
{| style="border:1px solid #BBB;margin:.46em 0 0 .2em"
|- style="font-size:86%"
|- style="font-size:86%"
| valign="top" |[[Image:01112017 photo AuNP Alanine.jpg‎|180px]] [[Image:01112017 AuNP Ala.png‎|180px]]
| valign="top" |[[Image:01112017 photo AuNP Valine.jpg‎|300px]] [[Image:01112017 AuNP Val.png‎|300px]]
|}
|}


Latest revision as of 02:11, 27 September 2017

Biomaterials Design Lab Main project page
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Objective

An analysis of Nanoparticle synthesis (taking pictures and recording UV-Vis) gathered on both the 11th and 12th is presented here. The reactions were run on the 5th (100 uM amino acid) and the 11th (25, 50, 150, and 200 uM).

Description

  1. Add experimental record here. Include what, how, and why...

Data

All data are shown with Alanine at 25uM to indicate what "no reaction" looks like.

Alanine

Arginine

Asparagine

Aspartic Acid

Note: I think that aspartic acid is an outlier because it has an N-methyl protecting group instead of an N-acetyl protecting group. My hunch is that Aspartic acid won't make nanoparticles with different N-protection.

Cysteine

Glutamine

Glutamic Acid

Glycine

Histidine

Isoleucine

Leucine

Lysine

Note: this data for Nα-acetyl lysine doesn't match with my previous data for lysine. I think that the primary amine on the side chain may also be protected. I need to check into this.

Methionine

Phenylalanine

Proline

Serine

Threonine

Tryptophan

Tyrosine

Valine

Notes

This area is for any observations or conclusions that you would like to note.


Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.




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