A new peptide-based method for the design and synthesis of nanoparticle superstructures: Construction of highly ordered gold nanoparticle double helices

Article abstract of DOI:10.1021/ja805683r

Left-handed gold nanoparticle double helices were prepared using a new method that allows simultaneous synthesis and assembly of discrete nanoparticles. This method involves coupling the processes of peptide self-assembly of and peptide-based biomineraliz

Full text of DOI:10.1021/ja805683r

Published on Web 09/19/2008
A New Peptide-Based Method for the Design and Synthesis of Nanoparticle
Superstructures: Construction of Highly Ordered Gold Nanoparticle Double
Helices
Chun-Long Chen,† Peijun Zhang,‡ and Nathaniel L. Rosi*,†
Department of Chemistry, UniVersity of Pittsburgh, 219 Parkman AVenue, and Department of Structural Biology,
UniVersity of Pittsburgh School of Medicine, 3501 5th AVenue, Pittsburgh, PennsylVania 15260
Received July 21, 2008; E-mail: nrosi@pitt.edu
Inorganic nanoparticles are widely considered potential structural
and functional building-blocks for new technologically significant
materials.1-5 Many properties of these materials are predicted to
depend not only on the size, shape, and composition of the
nanoparticle building blocks but also to a large extent on the spatial
arrangement of these building blocks with respect to one another
within a material.1,2,5 Recently, significant effort has been directed
toward assembling nanoparticles into sophisticated structures.3,6-20
Examplesofsometypicalmethodsincludecolloidalcrystallization,3,6-9
molecular templating strategies,10-13 or directional assembly of
multivalent nanoparticles.14-18 Despite these advances, assembling
nanoparticles into well-defined superstructures amenable to practical
use still remains a significant challenge, and the development of
more facile and efficient methods for rationally designing and
fabricating such structures is critically important for the continued
advancement of this area. Here we report a new peptide-based
method to address this challenge: a one-pot direct approach that
couples peptide self-assembly and peptide-based biomineralization
into one simultaneous process. In this method, peptide self-
assembly, nucleation and growth of particular nanoparticles, the
topology of the resultant nanoparticle superstructure, and the precise
stereochemical arrangement of nanoparticles within the structure
are programmed by rationally designing specific peptide-conjugates.
We demonstrate the utility of this method by preparing an
unprecedented left-handed gold nanoparticle double-helical struc-
ture. We expect that this assembly strategy will allow for the rational
design of a variety of relatively complex nanoparticle superstruc-
tures and broaden the scope of “bottom-up” fabrication approaches.
Two research developments contributed to the conception of the
methodology reported herein: (1) the study and manipulation of
peptide self-assembly21-24 and (2) the in vitro evolution of specific
peptides for mineralizing and recognizing specific inorganic
materials.25-29 The former has become a broad field, and various
strategies have emerged that allow for the design of peptide-based
supramolecular materials. In some cases, the native secondary
structure of the peptides, such as R-helix or ꢀ-sheet motifs, strongly
impact structure formation while in other cases, synthetic modifica-
tions to the peptide, such as attachment of organic molecule
appendages to the peptide terminus, help promote assembly of
certain structures. To date, many ordered peptide assemblies,
including some that adopt micellar, vesicular, tubular, helical, or
membrane architectures, have been reported.21-24 The latter
development has led to the discovery of numerous oligopeptides
that recognize and bind particular inorganic materials in a sequence-
specific fashion. For example, peptides that exhibit high binding
affinities for gold, silver, zinc sulfide, and other inorganic materials
have been identified.28 In some cases, these peptides play a
significant role in controlling the nucleation and growth of particular
nanoparticles from precursor salt solutions.26 In this study we show
that these two processes, peptide self-assembly and peptide-based
nucleation of discrete nanoparticles, can be coupled to occur
simultaneously, resulting in a facile method for controlling the
synthesis and hierarchical assembly of nanoparticles.
To demonstrate the feasibility of this method, we began by first
attaching small organic molecules to peptide AYSSGAPPMPPF
and then investigating the assembly of the resultant peptide-
conjugates. AYSSGAPPMPPF, hereafter referred to as PEPAu, was
evolved and isolated via phage-display methods to have a high
affinity for gold surfaces.26 In the presence of chloroauric acid and
HEPES buffer, PEPAu assists the formation of monodisperse
spherical gold nanoparticles through a process that involves both
the tyrosine residue and HEPES.26,30-33 Given the hydrophilic
nature of PEPAu, we reasoned that attaching an aliphatic carbon
tail to its N-terminus would promote its assembly into various
multidimensional supramolecular assemblies, such as 1-D peptide
amphiphile structures.23,34 As a first step in this direction, we
coupled succinimide-activated dodecanoic acid to the N-terminus
of PEPAu to generate [C11H23CO]-PEPAu, or C12-PEPAu (Supporting
Information, Figures S1, S2). C12-PEPAu was completely dissolved
in 0.1 M HEPES buffer, conditions that allow for both C12-PEPAu
self-assembly as well as gold nanoparticle nucleation.26 To gain
insight into the structure of the peptide-amphiphile assembly, we
examined the assembled structures using transmission electron
microscopy (TEM) and tapping-mode atomic force microscopy
(AFM). TEM images (Figure 1a) revealed the presence of uniform
individual fibers with micrometer lengths (>4 µm) and narrow (6.1
( 0.6 nm) widths (Figure S11). Using tapping-mode AFM, we
determined that each fiber adopts a twisted-ribbon morphology and
that the ribbons appear to twist in a left-handed direction (Figure
1b and Figures S4, S5). The pitch of the twisted-nanoribbon was
consistently measured to be 84.1 ( 4.2 nm (Figure 1c and Figures
S4, S11). Such uniform peptide-nanoribbons are very unusual.
Spectroscopic studies were performed to better understand the
structure of the helical fibers. Specifically, we examined the fibers
using circular dichroism (CD) spectroscopy (Figure S6) and
observed a peak around 227 nm, which could correspond to the
signal produced by ꢀ-sheet structures.34 To further probe whether
ꢀ-sheet formation occurs, we analyzed the assembled species using
Fourier transform infrared (FT-IR) spectroscopy (Figure S7). The
peak at 3275 cm-1 corresponds to the stretching frequency of
hydrogen-bonded N-H groups. The amide I band (1626 cm-1) is
consistent with ꢀ-sheet conformations,35,36 and the C-H vibration
bands at 2918 cm-1 and 2850 cm-1 indicate ordered packing of
the aliphatic chains.37
† Department of Chemistry.
‡ Department of Structural Biology.
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2008 American Chemical Society
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C O M M U N I C A T I O N S
Figure 2. TEM characterization of gold nanoparticle double helices.
Structurally regular gold nanoparticle double helices form when a solution
of chloroauric acid is added to HEPES buffer solutions containing
C12-PEPAu, as evidenced by TEM analysis (a-d). The sizes of the gold
nanoparticles are uniform (8.2 ( 1.0 nm; based on 150 counts) (e).
Figure 1. C12-PEPAu fiber characterization and model of assembly. TEM
images reveal that C12-PEPAu amphiphiles assemble into uniform fibers
(width ) 6.1 ( 0.6 nm; based on 60 counts) in HEPES buffer solutions
(a). These fibers have twisted-ribbon morphologies, as evidenced by tapping-
mode AFM height images (b,c). The twisted nanoribbons have a regular
pitch of 84.1 ( 4.2 nm, as determined by AFM height images (based on
60 counts) (d). C12-PEPAu units assemble into left-handed twisted nano-
ribbons (e).
Figure 3. Electron tomography data (a,b) and schematic depiction of the
formation of gold nanoparticle double helices (c). The structure of a gold
nanoparticle double helix is confirmed using electron tomography. X-Y
computational slices (a, I-VIII) of the 3-D tomographic volume containing
the double helical gold nanoparticle assembly and a 3-D surface rendering
of the tomographic volume (b) both reveal the left-handed nature of the
helices. Left-handed gold nanoparticle double helices are synthesized and
assembled directly in a reaction containing HEPES buffer solutions of
chloroauric acid and C12- PEPAu (c).
Using the spectroscopic and microscopy data, we arrived at a
working model for the structure of the nanoribbon assembly. Our
model (Figure 1e) is similar to previously developed models.23,34
The width of the nanoribbon is spanned by two C12-PEPAu units
that interact through their aliphatic tails. Organization of the
C12-PEPAu units along the longitudinal axis of the nanoribbon is
driven by the formation of parallel ꢀ-sheets and favorable hydro-
phobic interactions between the aliphatic tails. Given that the first
four amino acids (AYSS) have a propensity to form ꢀ-sheets
whereas proline residues do not,38 we propose that these amino
acids (AYSS) participate in ꢀ-sheet assembly and also likely impart
the left-handed helical twist to the nanoribbon.22,34 The formation
of nanoribbons can be attributed to the fact that the outer two-
thirds of the peptide sequence is relatively sterically bulky because
of the presence of two proline-proline dimers and one phenylalanine.
The steric bulk causes the C12-PEPAu units to assemble into
nanoribbon structures rather than condensed tubular micelles, while
at the same time PEPAu subunits effectively shield the hydrophobic
core of the nanoribbon. This working model is consistent with all
of our experimental observations.
acid (HAuCl4) were added to clear HEPES buffer solutions
containing C12-PEPAu which were carefully filtered to remove any
assembled structures. Immediately after the addition of HAuCl4,
TEM samples were prepared and their examination revealed that
the C12-PEPAu fibers formed even in the presence of the gold salt
(Figure S3). When the solutions were allowed to stand for ∼30
min, a small amount of precipitate formed. TEM studies of the
precipitate suggested formation of double-helical assemblies com-
prising uniform discrete spherical gold nanoparticles (Figure 2a-e
and Figure S10). A better understanding of the structure of the
nanoparticle assemblies was obtained from electron tomographic
analysis. A series of tilted images from -70° to +70° with 1° tilt
intervals were collected. These tilted projections were aligned and
combined computationally to reconstruct a three-dimensional
electron density map (tomogram). As illustrated in the tomographic
slices (Figure 3a) and in a 3-D surface rendering of the reconstructed
density map (Figure 3b), the gold nanoparticle assemblies are left-
handed double helices, which is in keeping with the observed
To determine whether the above process of peptide self-assembly
and the process of PEPAu biomineralization could be coupled into
one simultaneous process as a means to design and construct double-
helical gold nanoparticle superstructures, solutions of chloroauric
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C O M M U N I C A T I O N S
chirality of the twisted C12-PEPAu nanoribbons. The measured
maximum inner-distance between the particles along the width of
the double helix is 6.0 ( 0.8 nm, and the pitch of the double helix
is 83.2 ( 4.4 nm (Figure S11). Both distances are consistent with
the observed width and pitch of the twisted C12-PEPAu nanoribbons.
These observations all indicate that the synthesis of the nanoparticles
and the assembly of the nanoribbons are coupled and that the
peptide-conjugates successfully control the formation of gold
nanoparticle double helices (Figure 3c). The results of control
experiments help verify this conclusion. When identical syntheses
tion. They are grateful to the various support services provided by
the University of Pittsburgh’s Department of Chemistry, including
the glass shop, machine shop, and electronics shop. They also
acknowledge Dr. David Earl, Daniel Lamont, and Dr. Joel Gillespie
for fruitful discussions.
Supporting Information Available: Experimental procedures,
Figures S1-14, and additional supporting data. This material is
available free of charge via the Internet at http://pubs.acs.org.
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Acknowledgment. Funding for this work was provided by the
University of Pittsburgh. The authors thank the Department of
Mechanical Engineering and Materials Science for access to electron
microscopy instrumentation and the Petersen Institute for Nano-
science and Engineering (PINSE) for access to AFM instrumenta-
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