|
|
|
|
| LEADER |
01574 am a22002053u 4500 |
| 001 |
125797 |
| 042 |
|
|
|a dc
|
| 100 |
1 |
0 |
|a Wang, Wade
|e author
|
| 100 |
1 |
0 |
|a Massachusetts Institute of Technology. Department of Chemistry
|e contributor
|
| 100 |
1 |
0 |
|a Massachusetts Institute of Technology. Department of Chemical Engineering
|e contributor
|
| 100 |
1 |
0 |
|a Koch Institute for Integrative Cancer Research at MIT
|e contributor
|
| 700 |
1 |
0 |
|a Hammond, Paula T
|e author
|
| 245 |
0 |
0 |
|a Hydrolysis resistant functional polypeptide scaffold for biomaterials
|
| 260 |
|
|
|b Royal Society of Chemistry (RSC),
|c 2020-06-15T17:28:38Z.
|
| 856 |
|
|
|z Get fulltext
|u https://hdl.handle.net/1721.1/125797
|
| 520 |
|
|
|a For biomaterials, rich functionality often comes at a cost of precise control over structure. In this paper, we have developed a hydrolysis resistant polypeptide that marries the potential for expansive modification with synthetic control. This polymer, poly(γ-propargyl-l-glutamine) may be prepared from commercially available or previously synthesized poly(l-glutamate) by routine amide bond coupling reactions on a multi gram scale. Afterwards, the polymer may be altered to suit many applications through modification of the side chains or end group by orthogonal and quantitative reactions. The ease of synthesis and versatile nature of poly(γ-propargyl-l-glutamine) makes it a unique and ideal scaffold for biomaterial applications.
|
| 520 |
|
|
|a National Science Foundation, Department of Materials Research ((Award 1307064)
|
| 546 |
|
|
|a en
|
| 655 |
7 |
|
|a Article
|
| 773 |
|
|
|t Polymer Chemistry
|
