Discovery of a non-cationic cell penetrating peptide derived from membrane-interacting human proteins and its potential as a protein delivery carrier

Cell penetrating peptides (CPPs) are peptides that can be translocated into cells and used as a carrier platform for the intracellular uptake of cargo molecules. Subject to the source of CPP sequences and their positively charged nature, the cytotoxicity and immunogenicity of conventional CPPs needs to be optimized to expand their utility for biomedical applications. In addition to these safety issues, the stability of CPPs needs to be addressed since their positively charged residues are prone to interact with the biological milieu. As an effort to overcome these limitations of the current CPP technology, we isolated CPP candidate sequences and synthesized peptides from twelve isoforms of annexin, a family of membrane-interacting human proteins. The candidate screen returned a CPP rich in hydrophobic residues that showed more efficient cellular uptake than TAT-CPP. We then investigated the uptake mechanism, subcellular localization, and biophysical properties of the newly found CPP, verifying low cytotoxicity, long-term serum stability, and non-immunogenicity. Finally, model proteins conjugated to this peptide were successfully delivered into mammalian cells both in vitro and in vivo, indicating a potential use of the peptide as a carrier for the delivery of macromolecular cargos.

. Schematic presentation of annexin isoforms and their N-terminus interacting with plasma membrane Annexin proteins has 12 types in a human form. Structures of annexins are consists of 4-8 annexin repeats domain that has the endonexin fold (red blocks). Annexin III, IV, V, and VIII has a simple structure having 12-19 residues length of N-terminal domains while annexin XI has a longer length. Annexin I and II have amphipathic α -helices in N-terminus, with phosphorylation sites for serine, threonine, and tyrosine. A glutamine residue is a linking site of a transglutaminase at position 18 in annexin I. Annexin VII and XI has the long N-terminal domain which is composed with glycine, tyrosine, and proline residues (green letters). Annexin XIII is different from other annexins as it has a myristoylation (Myr) of N-terminal domain. All annexins can be transported in and out of plasma membrane via endocytosis or exocytosis with/without calcium ion. This figure describes the endogenous annexins, which has the interaction with extracellular membrane, as proven from the experiment using artificial membrane, such as multivesicular bodies (MVBs) 49 .
Scientific RepoRts | 5:11719 | DOi: 10.1038/srep11719 Results Design and preparation of CPP candidates. We designed CPP candidate sequences from cell penetrating moieties representing the membrane-interacting domains of the endogenous annexin family 21 (Fig. 1). The N-terminal regions of twelve annexin A isoforms (AA1H to AA13H in Table 1) were chosen as CPP candidates since the residues in this region are known to have calcium-sensitive lipid-binding or phospholipid-binding properties 15 . Interestingly, N-terminus sequences of annexin proteins are composed of hydrophobic residues with a charge of 0 to 1, unlike another well-known CPP, TAT, that has eight charged residues of arginine ( Table 1). The twelve CPP candidates were synthesized with a fluorescent label by using the standard Fmoc-based solid phase peptide synthesis protocol. All synthesized peptides were characterized by MALDI-TOF mass analysis (Table 1).

Cellular uptake of annexin A-derived CPPs.
The cellular uptake efficiency of the twelve candidate peptides into HeLa cells was tested using a flow cytometer ( Fig. 2A). Five candidates (AA3H, AA4H, AA5H, AA8H, and AA13H) were found to have cell-penetrating properties with a significant cellular uptake efficiency at 1 μ M. On further examination at various concentrations, dose-dependent cellular uptake efficiency and distinguished potency in intracellular translocation in the order of AA3H > AA5 H > AA8H > AA13H > AA4H were established (Fig. 2B). When the uptake efficiency of the most potent one, AA3H, was compared with that of the widely used conventional CPP TAT peptide (Fig. 2C), AA3H was delivered into the cells better than TAT. In contrast, when compared with the fully cationic R9 peptide, AA3H showed much lower cellular uptake ( Supplementary Fig. S1A). For assessing uptake of AA3H by confocal microscopy, HeLa cells were treated with AA3H and fluorescently analyzed. Z-stack images (30 sections) of selected cells were obtained ( Supplementary Fig. S2) and constituted into a 2.5D image of the cells. Fig. 2D clearly shows that AA3H (green color) resides inside the cell membrane (wheat germ agglutinin, red color), thereby confirming that the cytometry profiles obtained were not due to adsorption on the cell surface but to intracellular delivery of the peptide. Cellular uptake mechanism of AA3H. After settling on AA3H as the best CPP candidate, we investigated the uptake mechanism of the peptide by employing several well-established endocytosis inhibitors 22 because the internalization into mammalian cells of biomacromolecules such as peptides and proteins is mainly accomplished through endocytic mechanisms 23 . We first tested whether the cellular uptake of AA3H was affected by heparan sulfate proteoglycan (HSPG), a component involved in the initial step of membrane-CPP interaction 24 . After treatment with several concentrations of heparin sulfate for 30 min, HeLa cells were incubated with AA3H for 4 h. As shown in Fig. 3A, the intracellular delivery of the peptide decreased by 45% after treatment with 50 μ g/mL heparin sulfate, which was expected since most CPPs penetrate the cell membrane via HSPG-mediated pathways. Despite the presence of only one arginine in the AA3H sequence, the peptide still appeared to interact with HSPG during the initial step of penetration (Fig. 3A), probably due to a contribution by tryptophan, with the basic residue triggering glycosaminoglycan (GAG)-dependent endocytosis 25 . However, concentrations of heparin higher than 50 μ g/mL did not lead to an additional inhibition of peptide delivery, suggesting that the uptake may also be driven by interactions with other membrane components such as phospholipids. The phospholipids known to interact with annexin III, the parent protein of AA3H, were found to also bind AA3H ( Supplementary Fig. S3) 26 . This indicates that the binding preference of the protein is preserved in the peptide, probably contributing to the cell-penetrating properties of the peptide. Subsequently, we examined the effect of lowered temperature on the cellular penetration to test whether the translocation of the peptide is mediated via an energy-dependent pathway 27 . AA3H was incubated with HeLa cells at 4 °C for 2 h, and cellular uptake efficiency was analyzed by flow cytometry. As shown in Fig 3B, the cellular uptake of AA3H-CPP at 4 °C was approximately 66% lower than that at 37 °C (control), indicating that the peptide was internalized into cells via an energy-dependent endocytosis mechanism. To examine the details of the endocytosis mechanism, cells were pre-incubated with several inhibitors of distinct aspects of the endocytosis mechanism before treatment with AA3H (Fig. 3C). A 30-min pre-treatment of cells with chlorpromazine (CPZ), an inhibitor of clathrin-dependent endocytosis 28 , resulted in a 23.5% decrease in AA3H-CPP uptake. When chloroquine (CQ), a disruptor of endosome/ lysosome, was used instead, a 20.5% increase in mean fluorescence intensity was observed. However, this was not due to an increase of uptake but because of the dequenched intensity of fluorescein after escape from the acidic environment of the endosome, because pH-insensitive dye-labeled AA3H did not show any increased intensity upon treatment with CQ ( Supplementary Fig. S4). Treatment with methyl-β -cyclodextrin (Mβ CD) and nystatin (NYS), related to the caveolae-dependent mechanism, significantly reduced the uptake of the peptide by 32% and 15%, respectively. In an experiment to test the dynamin dependency of AA3H-CPP penetration by employing the specific inhibitor of dynamin, dynasore, a 57% decrease of the uptake was observed. A significant inhibition of peptide delivery was also obtained by treatment with 5-(N-ethyl-N-isopropyl) amiloride (EIPA), an inhibitor of macropinocytosis. These results indicate that the uptake of AA3H is not accomplished via a single mechanism but via a complex combination of various processes such as clathrin-mediated, caveolae-mediated endocytosis mechanisms and macropinocytosis. Subcellular localization of AA3H. Previously, many CPPs delivered by endocytosis have been generally destined for the lysosome for degradation, while several CPPs have been able to escape 29 . In particular, CPPs utilizing the caveolae-mediated pathway have been transferred into the Golgi apparatus or endoplasmic reticulum (ER) after invagination of the plasma membrane by dynamin action 29 . To see whether AA3H follows similar localization patterns, we attempted to trace the subcellular localization of the internalized peptide by confocal microscopy using organelle-specific fluorescent staining reagents. As shown in Fig. 4A, a certain amount of AA3H peptide was found in lysosomes (stained with Lysotracker), but not in the nucleus (stained with a Hoechst dye), indicating that the peptide may undergo partial decomposition in the lysosome. These results could explain the reduced accumulation of AA3H-CPP in lysosomes in the presence of an endosome/lysosome disrupter, as observed during flow cytometry analysis (Fig. 3C). However, no peptide was found in the ER and the Golgi when examined for localization in these subcellular organs using organ-specific binders labeled with a fluorescent protein (Fig. 4B,C). As membrane ruffling by actin rearrangement is required for the process of macropinocytosis, we tested for possible interactions of AA3H with actin and found partial colocalization in the cells (Fig. 4D). Overall, these results suggest that after caveolae-mediated endocytosis, the peptide seems to escape before entering ER and Golgi and is found in the cytoplasm. While AA3H does not enter the nucleus, a minor fraction of CPPs is found in the lysosome and plasma membrane, as inferred by the membrane-associating properties of annexin proteins 19 . In addition, our results are consistent with the previous finding that the hydrophobicity of a peptide improves its escape rate from endosomes 30 . The hydrophobic nature of Energy dependent penetration of AA3H. The relative penetration efficiency at the lowered temperature (4 °C, middle) was compared with that at 37 °C (right) (C) Delivery of AA3H into the cells pre-treated with endocytosis inhibitors. The delivery level of AA3H into untreated cells was used as the control and displayed as the gray bar. Each bar represents the average of three independent experiments.
AA3H may facilitate its uptake into the cytoplasm and the destabilization of the endosomal membrane for enhanced cytoplasmic release.

Conformation of AA3H.
After studying cellular uptake properties of AA3H, we investigated the conformational state of AA3H. CD spectra of AA3H revealed random coil and β -sheet structures. The profile shows a typical peak at around 196 nm as a positive band of β -sheet structure (Fig. 5, blue line). In contrast, the CD spectra of TAT showed a typical random coil structure with a strong negative band at 200 nm, supporting a previous report 31 (Fig. 5, red line). The CD profiles were similar at various concentrations of peptides, suggesting that there was no aggregation or dimerization. The conformation of the peptide is rather unusual since, according to previous reports 32 , most amphipathic CPPs show α -helical structures.
Analysis of serum stability of AA3H. Serum stability is an important precondition for applications of CPPs as delivery carriers in vitro and in vivo. The serum stability of AA3H was analyzed by determining the half-life of the peptide in mouse serum. Whereas TAT showed significantly lowered efficiency in the presence of serum (Fig. 6A, right), the delivery efficiency of AA3H was not considerably affected by the presence of serum (Fig. 6A, left). AA3H was incubated in serum solution at 37 °C, and the reaction was analyzed at various time points using reverse-phase HPLC for a time-course study of peptide degradation. Although AA3H showed gradual degradation over the incubation time, ca. 70%  of AA3H was still undamaged after 24 h (Fig. 6B), displaying much higher serum stability than other known CPPs 33 . This is consistent with the observation that cellular uptake of AA3H was not reduced in serum-containing medium (Fig. 6A).

Analysis of cellular toxicity and immunogenicity of AA3H-CPP. Subject to size and sequence
of CPPs, peptides can exhibit cytotoxicity and immunogenicity as potential risks for their biomedical applications. In order to evaluate the potential toxicity of the peptide, HeLa cells were treated with 0.01-100 μ M AA3H for 24 h, and cell viability was determined by a cell-counting assay. The peptide affected the cell viability only negligibly at 10 μ M, indicating that AA3H is non-cytotoxic in the concentration range used for the cellular uptake experiments (Fig. 7A).
To assess the potential immunogenicity of AA3H, we treated macrophage cells with the peptide and quantified the cellular release of interleukin-6 (IL-6), which is secreted by macrophages and T cells to stimulate immune responses in an acute phase and the innate immune system 34 . After incubation of Raw 264.7 cells in the presence of 10 μ M AA3H for 24 h, the amount of IL-6 released into the culture medium was estimated using an ELISA kit and compared to the amount obtained from lipopolysaccharide (LPS)-treated cells as a positive control (Fig. 7B). While IL-6 secreted in response to LPS as a standard immunogenic material was determined as 373 pg/mL, AA3H-stimulated cells released 30 pg/mL of IL-6, similar to non-treated control cells (20 pg/mL), indicating that AA3H is a virtually non-immunogenic peptide. Therefore, this CPP shows a good potential as a safe carrier system in various in vivo applications. Intracellular delivery of functional proteins using AA3H as a carrier. To test the potential of AA3H as a carrier for protein delivery, the peptide was conjugated with two different functional proteins such as β -galactosidase and Cre recombinase, active in cytoplasm and nucleus, respectively. For conjugation, the transglutaminase reaction was used as previously reported, connecting the acyl group of glutamine residues in peptides with the amino group of lysine residues in proteins to form a γ -glutamyl-ε -lysine structure 35 . For enhanced efficiency of the conjugation reaction, a protein linking peptide (PLP) containing multiple arginine residues was incorporated into the AA3H sequence (Fig. 8A). The cellular uptake of PLP-conjugated CPPs was initially assessed by flow cytometry utilizing the fluorescence label of the peptide. PLP alone could also be delivered, probably because of multiple arginine residues in the linker, although the uptake efficiency was not as high as with AA3H conjugation (Fig. 8B). When cells treated with AA3H-conjugated β -galactosidase were incubated with the X-gal substrate 5-bromo-3-indolyl β -D-galactopyranoside, the blue color of the hydrolysis product generated by intracellularly delivered β -galactosidase was observed in cells under microscopic analysis and thus clearly indicated that the enzyme was successfully delivered into the cells (Fig. 8C, AA3H-β -gal). In contrast, enzyme conjugated with PLP alone did not show considerable activity due to inefficient delivery of the protein (Fig. 8C, β -gal). Even TAT-conjugated enzyme was not delivered as efficiently as the AA3H-conjugated one, producing a relatively smaller amount of the colored product (Fig. 8C, TAT-β -gal). Uptake of β -galactosidase was additionally confirmed by measuring enzyme activity with an assay using the chromogenic substrate o-nitrophenyl-β -galactoside and reading absorbance at 405 nm. In this assay, β -galactosidase delivered by AA3H produced 298 pg/mL of o-nitrophenol, a 6-fold higher amount than obtained with the enzyme delivered by TAT (47 pg/mL) (Fig. 8D).
After demonstrating the feasibility of protein delivery based on AA3H, we attempted to deliver another functional protein, Cre recombinase (Cre), to confirm the utility of the peptide as a general carrier for the delivery of macromolecules. Cre is an enzyme that performs a recombination reaction between two specific recognition sites called loxP. To test intracellular activity of Cre, we prepared fibroblast cells containing plasmids that can be recombined by the enzyme to express red fluorescence protein (RFP) (Fig. 9A) 36 . After confirming uptake of CPPs into the fibroblasts (Fig. 9B), we prepared CPP-conjugated Cre using the same procedure as for CPP-conjugated β -galactosidase. After treatment of the cells with CPP-Cre conjugates, the expression level of RFP, as reflecting the activity of the enzyme, was monitored using confocal microscopy (Fig. 9C). Again, AA3H conjugation yielded higher RFP expression than TAT conjugation. When analyzed using a flow cytometer for quantitative comparison, CPP-Cre conjugates penetrated into primary fibroblast cells as well as in HeLa cells (Fig. 9D, top). Cells treated with AA3H-conjugated Cre exhibited a 2.1-times higher RFP expression level than cells treated with the TAT-conjugated enzyme (Fig. 9D, bottom). In vivo delivery of β-galactosidase by using AA3H as a carrier. Finally, biodistribution of a cargo protein by AA3H was assessed to examine whether the carrier property of the peptide observed at the in vitro level could be reproduced in vivo. After intraperitoneal administration of AA3H-β -gal to mice, main organs were harvested and treated with X-gal to estimate the amount of the delivered enzyme in each organ. The enzyme was detected in main organs except the brain (Fig. 10A). Histological analysis of tissue sections using microscopy indicated successful in vivo delivery of the protein with AA3H as a carrier (Fig. 10B). However, when compared with TAT-β -gal quantitatively with enzyme assays for tissue lysates, AA3H-β -gal was delivered less than TAT-β -gal in all organs in vivo. This is possibly due to the much slower uptake kinetics of AA3H with ~2 h of t 0.5 (half-time of internalization) compared to TAT with 1 min of t 0.5 37 , which allows AA3H to be cleared by body fluid around tissues before translocation into cells (Fig. 10C). Therefore, the improved intracellular uptake efficiency of AA3H-β -gal compared to TAT-β -gal observed in vitro could not be reproduced under in vivo conditions. Nevertheless, these data qualify the CPP AA3H as a molecular carrier, demonstrating successful protein delivery based on AA3H and suggesting that our newly found CPP has a great potential to be used for delivery of various functional macromolecules in vitro and in vivo.

Discussion
Since the first discovery of TAT, many CPPs were introduced as drug delivery platforms 38 , therapeutic agents [39][40][41] , and imaging probes in vivo 42 . These CPPs are either positively charged with multiple cationic residues or based on sequences of non-human organisms [43][44][45] . Membrane-interacting proteins can be considered a good potential source for discovery of new CPP sequences since membrane interaction is the initial step of the cell-penetrating process. Previously, a non-cationic CPP was obtained from a membrane protein of Mycobacterium tuberculosis 10 , while no CPPs have been identified from membrane-binding human proteins. To circumvent potential risks posed by sequences of non-human organisms such as bacteria and viruses, developing CPPs originated from human proteins is immensely important because CPPs with inherently human-friendly sequences would be preferable for practical use in the clinic.
AA3H showed higher serum stability than TAT, rendering it attractive for in vivo applications. Since proteolytic degradation of peptides in serum depends partly on their content of arginine and lysine residues 46 , the relatively hydrophobic AA3H peptide, containing only one arginine residue, could thus be a less preferred substrate for proteases than TAT, containing six arginine and two lysine residues. Whereas D-amino acids could be considered an alternative for preparation of CPPs to increase serum stability, such non-natural peptide backbones would be costly and may cause potential side-effects such as undesired immune responses 47,48 , making natural backbones more desirable for biomedical applications.
AA3H was a far better carrier than TAT for intracellular delivery of functional proteins in vitro. This unexpected difference may not have just been caused by a higher penetrating ability of AA3H but also by a difference in efficiency of the conjugation reaction. In contrast to a lack of lysine in the AA3H sequence, the TAT sequence contains both lysine and arginine residues required for conjugation by transglutaminase, thereby possibly yielding undesired self-conjugated products. The lack of lysine in AA3H is particularly advantageous if CPP conjugation with cargo proteins is performed using transpeptidase rather than cloning and expression of CPP-fused protein. When we used CPP-protein conjugates purified by removing peptides and possible TAT dimers, we could still observe higher protein delivery efficiency by AA3H compared to TAT (Supplementary Fig. S5), confirming that AA3H is more effective than TAT as a vehicle for intracellular protein delivery. Although in vivo delivery efficiency by these CPPs was not identical to that observed at the in vitro level, successful biodistribution of AA3H-conjugated protein clearly illustrates that this peptide could be utilized not only for in vitro but also for in vivo applications.
In summary, we have designed CPP candidate sequences from N-terminal sequences of annexin, a human protein family. After synthesis of the sequences, we found a novel CPP named AA3H, composed of hydrophobic sequences recruited from a membrane-interacting human protein, showing excellent cell penetrating ability. Cellular uptake of the peptide was mediated by various endocytosis mechanisms. The peptide was localized in the cytoplasm but not in the nucleus. According to CD spectra, the peptide showed a β -sheet conformation, which is unlike that of previously known amphipathic CPPs. The biophysical properties of the new peptide such as high serum stability, non-immunogenicity, and non-cytotoxicity appear beneficial for biomedical applications. Utility of the CPP as a carrier for biomacromolecules has been successfully demonstrated by the delivery of two functional proteins, β -galactosidase and Cre recombinase, both in vitro and in vivo. We therefore expect the newly found CPP AA3H to provide a useful delivery platform for various in vitro and in vivo applications. Peptide synthesis. Peptides were synthesized at a 25-μ mol scale using the standard Fmoc-based solid-phase peptide synthesis on Rink amide resin (0.7 mmol/g). For coupling reactions, Fmoc-protected amino acids (5 equivalents), HOBt (5 equivalents), HBTU (5 equivalents), and DIPEA (5 equivalents) in DMF were added to the solution of resin in DMF (0.5 mL). Deprotection of Fmoc was achieved by incubation of the resin with 20% (v/v) piperidine in DMF (0.5 mL) at room temperature for 30 min. After N-terminal FITC labeling, peptides were deprotected and cleaved from resin by incubation in deprotection solution (1 mL; 95% (v/v) TFA, 2.5% TIS, and 2.5% H 2 O) at room temperature for 2 h. Peptides were precipitated by addition of diethyl ether (5 mL), centrifuged at 1,500 × g for 5 min, and purified on C18 reversed-phase (RP) HPLC (Agilent Technologies, Santa Clara, CA, USA) using acetonitrile and water containing 0.1% TFA as eluents. All purified peptides were characterized using MALDI-TOF mass spectrometry (Kangwon National University, Kangwon, Korea).

Cells and cell culture. Human cervical carcinoma-derived HeLa cells were obtained from American
Type Culture Collection (ATCC) and maintained in DMEM supplemented with 10% fetal bovine serum (FBS), 1% penicillin, and 1% streptomycin (Gibco, Carlsbad, CA, USA) at 37 °C with 5% CO 2 in a humidified incubator. Murine macrophage cells (Raw 264.7) were cultured under identical conditions. pCALNL-DsRed cells were prepared as previously described 36 and maintained in DMEM with 10% FBS.

Cellular uptake and localization of CPPs.
For assessing the uptake of CPP candidates by HeLa cells, cells were seeded onto 6-well plates (1.0 × 10 6 cells/well). After 24 h, cells were washed two times with serum-free DMEM and incubated with CPPs at indicated concentrations (0.1, 1, 10 μ M) in serum-containing DMEM at 37 °C. Cells were washed two times with phosphate-buffered saline (PBS), incubated in trypsin-EDTA solution (0.01% trypsin) at 37 °C for 10 min to digest extracellular proteins, washed two times with ice-cold PBS, and finally resuspended in 500 μ L of ice-cold PBS for flow cytometry assays. For endocytosis inhibitor treatments, cells were pre-incubated with various inhibitors (50 μ g heparin, 50 μ M CPZ, 100 μ M CQ, 1 mM Mβ CD, 30 μ g dynasore, or 50 μ M EIPA) in serum-containing medium for 30 min before AA3H (1 μ M) was added. The sample for flow cytometry analysis was prepared as described above. For the analysis of peptide internalization, a GUAVA flow cytometry system (Merck Millipore, Darmstadt, Germany) with the FL-1 channel for measuring fluorescence in GuavaSoft 2.6 was used according to the manufacturer's instructions. Results were presented as a relative percentage value of untreated HeLa cells displayed as mean ± standard deviation (SD).
To visualize the cellular uptake of a peptide using confocal fluorescence microscopy, HeLa cells were seeded onto confocal bottom dish 35-mm plates (SPL, Gyeonggi-do, Korea) and incubated with AA3H (1 μ M) for 4 h. Lysosomes and nuclei of AA3H-treated cells were stained with LysoTracker (Life Technologies, Carlsbad, CA, USA; 1 μ g/mL for 30 min) and Hoechst (1 μ g/mL for 5 min), respectively. For staining ER and Golgi, CellLight Reagents BacMam 2.0 (Life Technologies, Carlsbad, CA, USA) were used. Cells were cultured in confocal dishes for 24 h, transfected with red fluorescence protein (RFP) for 24 h, and treated with AA3H (1 μ M) for 4 h. After washing two times with PBS, the intracellular fluorescence of HeLa cells was imaged using confocal laser scanning microscopy (LSM 700, Carl Zeiss, Jena, Germany). Circular dichroism (CD) spectroscopic measurements. CD spectra were recorded at 20 °C using a Jasco J-715 spectrometer (JASCO, Great Dunmow, UK) equipped with a PFD-350S temperature controller. All experimental samples were measured in a 1-cm quartz cell using a 260-190 nm measurement range, 100 nm/min scanning speed, 0.2 nm pitch, 4 s response time, and 1.0 nm bandwidth. The baseline was established with phosphate buffer, recorded under the same conditions, and subtracted automatically. For measurements, peptides were diluted to a final concentration of 0.1 mg/mL in 10 mM phosphate buffer (pH 6.4). Every sample was measured eight times, and cuvettes were washed three times with Milli-Q deionized H 2 O before each measurement.
Serum stability assay. For intracellular uptake of CPPs in the presence of serum, cells were treated with peptides (1 μ M) with or without 10% serum (Gibco, Carlsbad, CA, USA) for 4 h and analyzed by flow cytometry. Samples were prepared as described for cellular uptake above. AA3H (10 μ M) was incubated in a serum solution at 37 °C for various periods (30 min, 2 h, 4 h, 8 h, and 24 h), and the mixture was analyzed by RP-HPLC using a C18 column (Agilent Technologies, Santa Clara, CA, USA).
Cell viability assay. Cell viability was assessed using the Cell Counting Kit 8 (CCK-8; Dojindo, Kumamoto, Japan). HeLa cells were seeded into a 96-well plate, cultured until 80% confluence, and treated with AA3H (0 to 100 μ M) for 24 h in DMEM containing 10% serum. WST-1 reagent (10 μ L) was added to each well, followed by incubation for 2 h. The absorbance of each well was determined at 450-650 nm using a microplate reader system (Molecular Devices, Sunnyvale, CA, USA). Cell viability was presented as a relative percentage value of untreated HeLa cells displayed as mean ± standard deviation (SD).
Immunogenicity assay. Raw 264.7 cells were seeded into 24-well plates and cultured for 24 h. Cells were grown to 80% confluence and treated with lipopolysaccharides (LPS, 10 μ g/mL) as a positive control. After incubation of AA3H peptide (10 μ M) with cells for 24 h, supernatants were transferred to 1.5 mL tubes and centrifuged at 10,000 × g for 10 min at 4 °C. For the detection of interleukin-6 (IL-6) a mouse IL-6 ELISA kit (Thermo Scientific, Waltham, MA, USA) was used. Results from triplicate experiments were analyzed by Prism software (GraphPad, La Jolla, CA, USA). Data are presented as mean ± standard deviation (SD).
In vitro delivery of β-galactosidase by CPPs. Each CPP-PLP was conjugated with β -galactosidase (5 mg/mL in DMF, Sigma Aldrich) using transglutaminase (1 mg/mL, Sigma Aldrich) in conjugation buffer (50 mM Tris-HCl pH7.4, 5 mM CaCl 2 , 1 mM DTT) for 1 h at 37 °C. Cells were washed twice with serum-free DMEM and incubated in a mixture of serum-free medium (400 μ L), the resulting conjugate solution (100 μ L) at 37 °C for 6 h, washed thrice with serum-free DMEM and analyzed using flow cytometry and confocal laser scanning microscopy at 37 °C for 3 h. For microscopic analysis, cells were fixed in 1× fixation buffer (2% formaldehyde and 0.2% glutaraldehyde in PBS) for 10 min and washed twice with PBS. Using a β -galactosidase staining kit (GALS, Sigma Aldrich, St. Louis, MO, USA), cells were incubated with X-gal substrate at 37 °C for 2 h and washed twice with PBS. Stained cells were analyzed using a Nuance microscope (Nuance, Olympus; 100 × oil immersions). To quantify the activity of delivered β -galactosidase, cells containing CPP-β -galactosidase conjugates were treated as described above, except using O-nitrophenyl-β -galactoside (ONPG, Sigma Aldrich, St. Louis, MO, USA) as the substrate instead of X-gal. Cells were lysed with RIPA lysis buffer at room temperature for 10 min and centrifuged at 12,000 × g for 5 min. Supernatants were incubated with ONPG substrate (in 1 mM MgCl 2 , 45 mM β -mercaptoethanol, 0.1 M sodium phosphate pH 7.4) in a 96-well plate at 37 °C for 30 min before adding stop solution (3,3' ,5,5'-tetramethylbenzidine, TMB; Thermo Scientific). Absorbance was measured at 405-420 nm using a spectrophotometer (Molecular Devices).
In vitro delivery of Cre-recombinase by CPPs. Cre recombinase was conjugated with CPPs as described for CPP-β -galactosidase conjugates. Recombinant Cre recombinase containing a nuclear localization sequence (NLS) was purchased from Excellgen (Rockville, MD, USA). Fibroblast cells transfected with pCALNL-DsRed were seeded into confocal bottom dishes, grown to 80% confluence, washed twice with serum-free DMEM, and 500 μ L of serum-free medium was added. A 100 μ L solution containing conjugation buffer, CPPs (1 μ M), 25 μ g Cre recombinase (5 mg/mL), and 4.8 μ g transglutaminase was incubated at 37 °C for 1 h. The resulting conjugates were added to the cells and incubated at 37 °C for 6 h. Cells were washed thrice with serum-free DMEM and analyzed using flow cytometry and confocal laser scanning microscopy.
In vivo distribution of β-galactosidase by CPPs. All experiments with live animals were performed in compliance with the relevant laws and institutional guidelines of Korea Institute of Science and Technology (KIST), and institutional committees have approved the experiments. Five weeks-old BALB/c mice were injected intraperitoneally with 300 μ g of CPP-β -galactosidase conjugates in 0.3 mL of PBS. After 2 h, mice were sacrificed and perfused. The main organs (brain, liver, lung, kidney, heart, and spleen) were harvested, washed with PBS, fixed in 0.25% glutaraldehyde and 1.5% formaldehyde for 2 h, and developed in 1 mg/mL X-gal staining solution at 37 °C overnight. For tissue sections, organs were cut into 15 μ m sections on a cryomicrotome, fixed, and stained as above. Sections were analyzed using microscopy (Nuance, Olympus; 10 × ). For quantitative enzyme assays, the excised tissues were homogenized under liquid nitrogen and lysed with lysis buffer (250 mM Tris-HCl, pH 7.2, 0.1% Triton X-100) on ice for 30 min. The lysed tissues were centrifuged at 12,000 × g for 10 min at 4 °C, and 100 μ L of supernatant from each sample with normalized total protein concentration was mixed with 100 μ L of assay buffer (200 mM sodium phosphate, pH 7.3, 2 mM MgCl 2 , 100 mM β -mercaptoethanol, 1.33 mg/ ml ONPG) and incubated at 37 °C for 30 min. Na 2 CO 3 (1 M) was added to the reaction mixtures, and absorbance was measured at 420 nm using a microwell plate reader (Molecular Devices).
Statistical analysis. Two-way analysis of variance (ANOVA) was used to establish the statistical significance of difference in terms of peptide and the effect of fused peptides for each parameter. P-value summary for each comparison with control was inserted in figures (***P < 0.001; *P < 0.05).