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Characterization of nanofibers formed by self-assembly of β -peptide oligomers using small angle x-ray scattering
Helical oligomers of β -peptides represent a particularly promising type of building block for directed assembly of organic nanostructures because the helical secondary structure can be designed to be very stable and because control of the β -amino acid sequence can lead to precise patterning of che...
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Published in: | The Journal of chemical physics 2008-09, Vol.129 (9), p.095103-095103-8 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Helical oligomers of
β
-peptides represent a particularly promising type of building block for directed assembly of organic nanostructures because the helical secondary structure can be designed to be very stable and because control of the
β
-amino acid sequence can lead to precise patterning of chemical functional groups over the helix surfaces. In this paper, we report the use of small angle x-ray scattering measurements (SAXS) to characterize nanostructures formed by the directed assembly of
β
-peptide
A
with sequence
H
2
N
-
β
3
hTyr
-
β
3
hLys
-
β
3
hPhe
-
ACHC
-
β
3
hPhe
-
ACHC
-
β
3
hPhe
-
β
3
hLys
-
ACHC
-
ACHC
-
β
3
hPhe
-
β
3
hLys
-
C
O
N
H
2
. Whereas prior cryo-TEM studies have revealed the presence of nanofibers in aqueous solutions of
β
-peptide
A
, SAXS measurements from the nanofibers were not well-fit by a form factor model describing solid nanofibers. An improved fit to the scattering data at high
q
was obtained by using a form factor model describing a cylinder with a hollow center and radial polydispersity. When combined with a structure factor calculated from the polymer reference interaction site model (PRISM) theory, the scattered intensity of x-rays measured over the entire
q
range was well described by the model. Analysis of our SAXS data suggests a model in which individual
β
-peptides assemble to form long cylindrical nanofibers with a hollow core radius of
15
Å
(polydispersity of 21%) and a shell thickness of
20
Å
. This model is supported by negative stain transmission electron microscopy. |
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ISSN: | 0021-9606 1089-7690 |
DOI: | 10.1063/1.2955745 |