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1.
Eur J Pharm Biopharm ; 86(2): 190-9, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23702274

ABSTRACT

The main objective of the current study was to investigate penetration of cell penetrating peptides (CPPs: TAT, R8, R11, and YKA) through skin intercellular lipids using (31)P magic angle spinning (MAS) solid-state NMR. In vitro skin permeation studies were performed on rat skin, and sections (0-60, 61-120, and 121-180µm) were collected and analyzed for (31)P NMR signal. The concentration-dependent shift of 0, 25, 50, 100, and 200mg/ml of TAT on skin layers, diffusion of TAT, R8, R11, and YKA in the skin and time dependent permeation of R11 was measured on various skin sections using (31)P solid-state NMR. Further, CPPs and CPP-tagged fluorescent dye encapsulate liposomes (FLip) in skin layers were tagged using confocal microscopy. The change in (31)P NMR chemical shift was found to depend monotonically on the amount of CPP applied on skin, with saturation behavior above 100mg/ml CPP concentration. R11 and TAT caused more shift in solid-state NMR peaks compared to other peptides. Furthermore, NMR spectra showed R11 penetration up to 180µm within 30min. The results of the solid-state NMR study were in agreement with confocal microscopy studies. Thus, (31)P solid-state NMR can be used to track CPP penetration into different skin layers.


Subject(s)
Cell-Penetrating Peptides/chemistry , Cell-Penetrating Peptides/metabolism , Skin/chemistry , Skin/metabolism , Animals , Fluorescent Dyes/chemistry , Fluorescent Dyes/metabolism , Lipids/chemistry , Liposomes/chemistry , Liposomes/metabolism , Magnetic Resonance Spectroscopy/methods , Permeability , Rats , Rats, Hairless
2.
ACS Nano ; 7(9): 7562-72, 2013 Sep 24.
Article in English | MEDLINE | ID: mdl-23977885

ABSTRACT

The designer self-assembling peptide RADA16-I forms nanofiber matrices which have shown great promise for regenerative medicine and three-dimensional cell culture. The RADA16-I amino acid sequence has a ß-strand-promoting alternating hydrophobic/charged motif, but arrangement of ß-strands into the nanofiber structure has not been previously determined. Here we present a structural model of RADA16-I nanofibers, based on solid-state NMR measurements on samples with different schemes for (13)C isotopic labeling. NMR peak positions and line widths indicate an ordered structure composed of ß-strands. The NMR data show that the nanofibers are composed of two stacked ß-sheets stabilized by a hydrophobic core formed by alanine side chains, consistent with previous proposals. However, the previously proposed antiparallel ß-sheet structure is ruled out by measured (13)C-(13)C dipolar couplings. Instead, neighboring ß-strands within ß-sheets are parallel, with a registry shift that allows cross-strand staggering of oppositely charged arginine and aspartate side chains. The resulting structural model is compared to nanofiber dimensions observed via images taken by transmission electron microscopy and atomic force microscopy. Multiple NMR peaks for each alanine side chain were observed and could be attributed to multiple configurations of side chain packing within a single scheme for intermolecular packing.


Subject(s)
Nanofibers/chemistry , Nanofibers/ultrastructure , Peptides/chemistry , Amino Acid Sequence , Crystallization , Drug Design , Materials Testing , Molecular Sequence Data , Multiprotein Complexes/chemistry , Multiprotein Complexes/ultrastructure , Protein Conformation
3.
Biophys J ; 105(1): 222-30, 2013 Jul 02.
Article in English | MEDLINE | ID: mdl-23823242

ABSTRACT

MAX8, a designer peptide known to undergo self-assembly following changes in temperature, pH, and ionic strength, has demonstrated usefulness for tissue engineering and drug delivery. It is hypothesized that the self-assembled MAX8 nanofiber structure consists of closed ß-hairpins aligned into antiparallel ß-sheets. Here, we report evidence from solid-state NMR spectroscopy that supports the presence of the hypothesized ß-hairpin conformation within the nanofiber structure. Specifically, our (13)C-(13)C two-dimensional exchange data indicate spatial proximity between V3 and K17, and (13)C-(13)C dipolar coupling measurements reveal proximity between the V3 and V18 backbone carbonyls. Moreover, isotopic dilution of labeled MAX8 nanofibers did not result in a loss of the (13)C-(13)C dipolar couplings, showing that these couplings are primarily intramolecular. NMR spectra also indicate the existence of a minor conformation, which is discussed in terms of previously hypothesized nanofiber physical cross-linking and possible nanofiber polymorphism.


Subject(s)
Nanofibers/chemistry , Peptides/chemistry , Amino Acid Sequence , Hydrogen-Ion Concentration , Magnetic Resonance Spectroscopy , Models, Molecular , Protein Structure, Secondary
4.
J Pept Sci ; 19(8): 477-84, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23801546

ABSTRACT

Solid state NMR measurements on selectively (13) C-labeled RADA16-I peptide (COCH3 -RADARADARADARADA-NH2 ) were used to obtain new molecular level information on the conversion of α-helices to ß-sheets through self-assembly in the solid state with increasing temperature. Isotopic labeling at the A4 Cß site enabled rapid detection of (13) C NMR signals. Heating to 344-363 K with simultaneous NMR detection allowed production of samples with systematic variation of α-helix and ß-strand content. These samples were then probed at room temperature for intermolecular (13) C-(13) C nuclear dipolar couplings with the PITHIRDS-CT NMR experiment. The structural transition was also characterized by Fourier transform infrared spectroscopy and wide angle X-ray diffraction. Independence of PITHIRDS-CT decay shapes on overall α-helical and ß-strand content infers that ß-strands are not observed without association with ß-sheets, indicating that ß-sheets are formed at elevated temperatures on a timescale that is fast relative to the NMR experiment. PITHIRDS-CT NMR data were compared with results of similar measurements on RADA16-I nanofibers produced by self-assembly in aqueous salt solution. We report that ß-sheets formed through self-assembly in the solid state have a structure that differs from those formed through self-assembly in the solution state. Specifically, solid state RADA16-I self-assembly produces in-register parallel ß-sheets, whereas nanofibers are composed of stacked parallel ß-sheets with registry shifts between adjacent ß-strands in each ß-sheet. These results provide evidence for environment-dependent self-assembly mechanisms for RADA16-I ß-sheets as well as new constraints on solid state self-assembled structures, which must be avoided to maximize solution solubility and nanofiber yields.


Subject(s)
Peptides/chemistry , Amyloid beta-Peptides/chemistry , Humans , Magnetic Resonance Spectroscopy/standards , Nanofibers/chemistry , Peptide Fragments/chemistry , Protein Refolding , Protein Structure, Quaternary , Protein Structure, Secondary , Reference Standards , Solutions , Spectroscopy, Fourier Transform Infrared , X-Ray Diffraction
5.
Biomacromolecules ; 13(6): 1794-804, 2012 Jun 11.
Article in English | MEDLINE | ID: mdl-22559149

ABSTRACT

We report that synthetic RADA16-I peptide transforms to ß-strand secondary structure and develops intermolecular organization into ß-sheets when stored in the solid state at room temperature. Secondary structural changes were probed using solid state nuclear magnetic resonance spectroscopy (ssNMR) and Fourier transform infrared spectroscopy (FTIR). Intermolecular organization was analyzed via wide-angle X-ray diffraction (WAXD). Observed changes in molecular structure and organization occurred on the time scale of weeks during sample storage at room temperature. We observed structural changes on faster time scales by heating samples above room temperature or by addition of water. Analysis of hydration effects indicates that water can enhance the ability of the peptide to convert to ß-strand secondary structure and assemble into ß-sheets. However, temperature dependent FTIR and time dependent WAXD data indicate that bound water may hinder the assembly of ß-strands into ß-sheets. We suggest that secondary structural transformation and intermolecular organization together produce a water-insoluble state. These results reveal insights into the role of water in self-assembly of polypeptides with hydrophilic side chains, and have implications on future optimization of RADA16-I nanofiber production.


Subject(s)
Nuclear Magnetic Resonance, Biomolecular , Peptides/chemical synthesis , Peptides/chemistry , Protein Structure, Secondary , Temperature
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