Amphiphilic Polyethylene-b-poly(L-lysine) Block Copolymer: Synthesis, Self-Assembly, and Responsivity

Polyethylene-b-polypeptide copolymers are biologically interesting, but studies of their synthesis and properties are very few. This paper reports synthesis and characterization of well-defined amphiphilic polyethylene-block-poly(L-lysine) (PE-b-PLL) block copolymers by combining nickel-catalyzed living ethylene polymerization with controlled ring-opening polymerization (ROP) of ε-benzyloxycarbonyl-L-lysine-N-carboxyanhydride (Z-Lys-NCA) and sequential post-functionalization. Amphiphilic PE-b-PLL block copolymers self-assembled into spherical micelles with a hydrophobic PE core in aqueous solution. The pH and ionic responsivities of PE-b-PLL polymeric micelles were investigated by means of fluorescence spectroscopy, dynamic light scattering, UV-circular dichroism, and transmission electron microscopy. The variation of pH values led to the conformational alteration of PLL from α-helix to coil, thereby changing the micelle dimensions.


Introduction
As one of the most important plastics and resins, polyethylene (PE) has been widely applied in daily life because of its excellent chemical and mechanical properties [1,2]. Furthermore, PE also has two striking features: high hydrophobicity and flexibility. PE is a highly hydrophobic polymer because its polymer chain has no polar groups or unsaturated bonds. Additionally, PE also exhibits high flexibility because it shows a very low glass transition temperature (T g < −68 • C) [3]. Therefore, PE can be used as a featured polymer segment to construct block copolymer as functional PE-based polymeric materials [4,5].
In this paper, we report the synthesis and characterization of new amphiphilic polyethyleneblock-poly(L-lysine) (PE-b-PLL) diblock copolymers by a tandem synthetic strategy by combining nickel-catalyzed living ethylene polymerization with controlled ring-opening polymerization (ROP) of ε-benzyloxycarbonyl-L-lysine-N-carboxyanhydride (Z-Lys-NCA) and sequential postfunctionalization. These block segments of PE-b-PLL copolymers have vastly different properties, such as solubility in solvents and secondary conformational states, which endow the amphiphilic block copolymer with rich phase behaviors. The self-assembly and pH and ionic responsivities of PE-b-PLL copolymers in aqueous solution were investigated for a better understanding of their potential applications.
In this paper, we report the synthesis and characterization of new amphiphilic polyethylene-block-poly(L-lysine) (PE-b-PLL) diblock copolymers by a tandem synthetic strat egy by combining nickel-catalyzed living ethylene polymerization with controlled ring opening polymerization (ROP) of ε-benzyloxycarbonyl-L-lysine-N-carboxyanhydride (Z-Lys-NCA) and sequential post-functionalization. These block segments of PE-b-PLL co polymers have vastly different properties, such as solubility in solvents and secondary conformational states, which endow the amphiphilic block copolymer with rich phase be haviors. The self-assembly and pH and ionic responsivities of PE-b-PLL copolymers in aqueous solution were investigated for a better understanding of their potential applica tions.

Synthesis and Characterization of PE-b-PLL Block Copolymer
PE-b-PLL block copolymers were prepared by combining nickel-catalyzed living eth ylene polymerization and ring-opening polymerization (ROP) of Z-Lys-NCA followed by deprotection of the benzyloxycarbonyl groups (Scheme 1). First, PE block was prepared by living ethylene polymerization with amine-imine nickel catalyst developed by our group [34][35][36][37][38][39][40][41]. ZnEt2 as a chain transfer agent (CTA) was then charged into a catalytic system, and subsequent workup involving oxidation and hydrolysis reactions produced a hydroxyl-terminated polyethylene (PE-OH) with number-average molecular weight o 17 kg/mol (degree of polymerization (DP) = 607) and narrow polydispersity index (PDI of ~1.02 ( Figure 1) determined by gel permeation chromatography (GPC) [25,[42][43][44]. PE-OH was converted to amino-terminated polyethylene (PE-COOCH( i Pr)NH2) by end-cap ping PE-OH with N-tert-butoxycarbonyl-L-valine (BOC-L-valine) and deprotecting BOC group [26,45]. The complete conversion from hydroxyl to amino group was evidenced by the full disappearance of the characteristic triplet peak of -CH2OH at 3.65 ppm and the complete disappearance of methyl signal of COOC(CH3)3 group at 1.46 ppm in the 1 H NMR spectroscopies ( Figure S1) [26].   Second, the PE macroinitiator (PE-COOCH( i Pr)NH2) was used to initiate the ROP of Z-Lys-NCA. Three polyethylene-b-poly(Z-Lys-NCA) (PE-b-PZL) copolymers were synthesized by adjusting the ratio of NCA monomer/macroinitiator. GPC curves of ROP polymerization products showed unimodal distributions (PDI = 1.3-1.4) (Figure 1), while copolymer molecular weights were not accurately determined because of the strong interactions between the polypeptides and GPC columns [26]. The block copolymers were further purified by precipitation from petroleum ether. The chemical structure of the block copolymer was proved by 1 H NMR spectrum based on the characteristic peaks of PZL at 3.10, 4.42, 5.09, and 7.61 ppm ( Figure 2). FT-IR analysis also supported the chemical structure of PE-b-PZL diblock copolymers ( Figure 2). The characteristic bands of amide group at ~1650 and 1545 cm −1 were clearly observed in the FT-IR spectrum ( Figure 3). Furthermore, the secondary conformation structures of PZL block were also proved by characteristic vibrational peaks [20,21]. In the vibrational range of the amide group, only two bands at 1650 (amide I) and 1550 cm −1 (amide II) were observed, strongly indicating that three block copolymer samples assumed α-helix conformation but no β-sheet conformation [25,46].  Second, the PE macroinitiator (PE-COOCH( i Pr)NH 2 ) was used to initiate the ROP of Z-Lys-NCA. Three polyethylene-b-poly(Z-Lys-NCA) (PE-b-PZL) copolymers were synthesized by adjusting the ratio of NCA monomer/macroinitiator. GPC curves of ROP polymerization products showed unimodal distributions (PDI = 1.3-1.4) (Figure 1), while copolymer molecular weights were not accurately determined because of the strong interactions between the polypeptides and GPC columns [26]. The block copolymers were further purified by precipitation from petroleum ether. The chemical structure of the block copolymer was proved by 1 H NMR spectrum based on the characteristic peaks of PZL at 3.10, 4.42, 5.09, and 7.61 ppm ( Figure 2). FT-IR analysis also supported the chemical structure of PE-b-PZL diblock copolymers ( Figure 2). The characteristic bands of amide group at 1650 and 1545 cm −1 were clearly observed in the FT-IR spectrum ( Figure 3). Furthermore, the secondary conformation structures of PZL block were also proved by characteristic vibrational peaks [20,21]. In the vibrational range of the amide group, only two bands at 1650 (amide I) and 1550 cm −1 (amide II) were observed, strongly indicating that three block copolymer samples assumed α-helix conformation but no β-sheet conformation [25,46]. Second, the PE macroinitiator (PE-COOCH( i Pr)NH2) was used to initiate the ROP of Z-Lys-NCA. Three polyethylene-b-poly(Z-Lys-NCA) (PE-b-PZL) copolymers were synthesized by adjusting the ratio of NCA monomer/macroinitiator. GPC curves of ROP polymerization products showed unimodal distributions (PDI = 1.3-1.4) (Figure 1), while copolymer molecular weights were not accurately determined because of the strong interactions between the polypeptides and GPC columns [26]. The block copolymers were further purified by precipitation from petroleum ether. The chemical structure of the block copolymer was proved by 1 H NMR spectrum based on the characteristic peaks of PZL at 3.10, 4.42, 5.09, and 7.61 ppm ( Figure 2). FT-IR analysis also supported the chemical structure of PE-b-PZL diblock copolymers ( Figure 2). The characteristic bands of amide group at ~1650 and 1545 cm −1 were clearly observed in the FT-IR spectrum ( Figure 3). Furthermore, the secondary conformation structures of PZL block were also proved by characteristic vibrational peaks [20,21]. In the vibrational range of the amide group, only two bands at 1650 (amide I) and 1550 cm −1 (amide II) were observed, strongly indicating that three block copolymer samples assumed α-helix conformation but no β-sheet conformation [25,46].   Third, amphiphilic PE-b-PLL block copolymers were prepared by hydrolysis reaction in the presence of acids (HBr/HAC) for deprotection of the benzyloxycarbonyl groups. PE-b-PLL diblock copolymers with pendant amino groups were easily soluble in water at weak acidic conditions (pH = 6.2), and pure PE-b-PLL copolymers extracted by water were used to study the structure characterization and properties in follow-up experiments. PEb-PLL copolymers were characterized by 1 H NMR spectrum in D2O. As shown in Figure  2, the characteristic resonances of PLL segment were observed, while no signals of PE block appeared because of the formation of the polymeric aggregates in water (see selfassembly below). In comparison with PE-b-PZL polymer precursor, PE-b-PLL copolymer did not show proton signals of amine (h), phenyl (g), or methylene (f) on the benzyloxycarbonyl group at 7.61, 7.29, or 5.09 ppm, strongly indicating full deprotection. As a result, amphiphilic PE-b-PLL copolymers with different PLL chain lengths were precisely prepared, and Table 1 summarizes their characterization results.

Self-Assembly of PE-b-PLL in Water
Amphiphilic PE-b-PLL copolymers with hydrophobic PE segments and hydrophilic PLL segments are expected to self-assemble spontaneously into polymeric aggregates in selective solvents. Three PE-b-PLL samples were directly dissolved in water at room temperature, and their aqueous solutions were used to study self-assembly.
The critical micelle concentrations (CMC) of three amphiphiles were first determined using pyrene as a fluorescent probe. Aqueous solutions of PE-b-PLL copolymers with different concentrations were prepared containing a constant pyrene probe concentration of Third, amphiphilic PE-b-PLL block copolymers were prepared by hydrolysis reaction in the presence of acids (HBr/HAC) for deprotection of the benzyloxycarbonyl groups. PE-b-PLL diblock copolymers with pendant amino groups were easily soluble in water at weak acidic conditions (pH = 6.2), and pure PE-b-PLL copolymers extracted by water were used to study the structure characterization and properties in follow-up experiments. PE-b-PLL copolymers were characterized by 1 H NMR spectrum in D 2 O. As shown in Figure 2, the characteristic resonances of PLL segment were observed, while no signals of PE block appeared because of the formation of the polymeric aggregates in water (see self-assembly below). In comparison with PE-b-PZL polymer precursor, PE-b-PLL copolymer did not show proton signals of amine (h), phenyl (g), or methylene (f) on the benzyloxycarbonyl group at 7.61, 7.29, or 5.09 ppm, strongly indicating full deprotection. As a result, amphiphilic PE-b-PLL copolymers with different PLL chain lengths were precisely prepared, and Table 1 summarizes their characterization results.

Self-Assembly of PE-b-PLL in Water
Amphiphilic PE-b-PLL copolymers with hydrophobic PE segments and hydrophilic PLL segments are expected to self-assemble spontaneously into polymeric aggregates in selective solvents. Three PE-b-PLL samples were directly dissolved in water at room temperature, and their aqueous solutions were used to study self-assembly.
The critical micelle concentrations (CMC) of three amphiphiles were first determined using pyrene as a fluorescent probe. Aqueous solutions of PE-b-PLL copolymers with different concentrations were prepared containing a constant pyrene probe concentration of 1 × 10 −6 mol/L. The I I /I III band intensity ratios of the pyrene emissions were plotted against the logarithm of amphiphile concentration [27]. As shown in Figure 4, PE 607 -b-PLL 275 copolymer showed a clear deflection point at its CMC of 0.040 mg/mL (7.6 × 10 −7 mol/L). It was also found that the CMC value decreased with decreasing length of PLL segment (Table 2) because of the low hydrophilic fraction in block copolymers. Generally, the three PE-b-PLL copolymers had very low CMC values (as low as 10 −7 mol/L) because the PE segment has high hydrophobicity and PE-b-PLL copolymers readily form stable aggregates in aqueous solutions. 1 × 10 −6 mol/L. The II/IIII band intensity ratios of the pyrene emissions were plotted against the logarithm of amphiphile concentration [27]. As shown in Figure 4, PE607-b-PLL275 copolymer showed a clear deflection point at its CMC of 0.040 mg/mL (7.6 × 10 −7 mol/L). It was also found that the CMC value decreased with decreasing length of PLL segment (Table 2) because of the low hydrophilic fraction in block copolymers. Generally, the three PE-b-PLL copolymers had very low CMC values (as low as 10 −7 mol/L) because the PE segment has high hydrophobicity and PE-b-PLL copolymers readily form stable aggregates in aqueous solutions.  Dynamic light scattering (DLS) experiments measured at 25 °C and 0.20 mg/mL were further used to study the self-assembly properties of block copolymers in water. At pH = 6.2, PE-b-PLL copolymers formed aggregates with an average hydrodynamic radius (Rh) in the range of 117 to 141 nm with unimodal size distributions (PDI < 0.15). It was observed that Rh of PE-b-PLL polymeric aggregates decreased from 141 to 117 nm with a decrease in the length of PLL building block, which was a result of increasing hydrophilic PLL fraction. Transmission electron microscopy (TEM) was used to directly visualize the selfassembled aggregates of PE-b-PLL block copolymers. As shown in Figure 5, PE607-b-PLL275 copolymer in water self-assembled to spherical micelles with uniform size. The average radius of micelles determined by TEM was ~110 nm, which was consistent with the value measured by DLS analysis.  Dynamic light scattering (DLS) experiments measured at 25 • C and 0.20 mg/mL were further used to study the self-assembly properties of block copolymers in water. At pH = 6.2, PE-b-PLL copolymers formed aggregates with an average hydrodynamic radius (R h ) in the range of 117 to 141 nm with unimodal size distributions (PDI < 0.15). It was observed that R h of PE-b-PLL polymeric aggregates decreased from 141 to 117 nm with a decrease in the length of PLL building block, which was a result of increasing hydrophilic PLL fraction. Transmission electron microscopy (TEM) was used to directly visualize the self-assembled aggregates of PE-b-PLL block copolymers. As shown in Figure 5, PE 607 -b-PLL 275 copolymer in water self-assembled to spherical micelles with uniform size. The average radius of micelles determined by TEM was~110 nm, which was consistent with the value measured by DLS analysis.

pH Responsivity of PE-b-PLL
As a kind of polyelectrolyte, PLL homopolymer has pH-responsive properties. Therefore, PE-b-PLL block copolymer is also expected to show pH responsivity. PE607-b-PLL275 was chosen as a representative sample to study pH responsivity. The effect of the pH value of the solution on the size of PE607-b-PLL275 was examined by DLS measurements. Figure 6A shows the pH-induced size changes on the hydrodynamic radius (Rh) of PE607b-PLL275 determined by DLS. Although a clear change of Rh with alternation of solution from basicity to acidity was observed, the unimodal size distributions (~0.14) still remained ( Figure 6B and Table S1). The Rh of PE607-b-PLL275 decreased with decreasing pH value from 9.0 (basicity) to 6.2 (near neutrality). When the pH value decreased from 6.2 to 1.5 (acidity), the Rh of PE607-b-PLL275 also decreased. Further decreasing the pH value from 1.5 to 0.5 (strong acidity) did not change the Rh. The biggest Rh was observed at near neutral solution (pH ≈ 7). TEM images (Figures 5 and 7) of polymeric micelles at different pH values also supported the pH-induced size change, and the biggest polymeric micelles were observed at pH of 6.2. These pH-induced changes of PE607-b-PLL275 polymeric micelle size are unique and different to previous studies [25,27,33].

pH Responsivity of PE-b-PLL
As a kind of polyelectrolyte, PLL homopolymer has pH-responsive properties. Therefore, PE-b-PLL block copolymer is also expected to show pH responsivity. PE 607 -b-PLL 275 was chosen as a representative sample to study pH responsivity. The effect of the pH value of the solution on the size of PE 607 -b-PLL 275 was examined by DLS measurements. Figure 6A shows the pH-induced size changes on the hydrodynamic radius (R h ) of PE 607 -b-PLL 275 determined by DLS. Although a clear change of R h with alternation of solution from basicity to acidity was observed, the unimodal size distributions (~0.14) still remained ( Figure 6B and Table S1). The R h of PE 607 -b-PLL 275 decreased with decreasing pH value from 9.0 (basicity) to 6.2 (near neutrality). When the pH value decreased from 6.2 to 1.5 (acidity), the R h of PE 607 -b-PLL 275 also decreased. Further decreasing the pH value from 1.5 to 0.5 (strong acidity) did not change the R h . The biggest R h was observed at near neutral solution (pH ≈ 7). TEM images (Figures 5 and 7) of polymeric micelles at different pH values also supported the pH-induced size change, and the biggest polymeric micelles were observed at pH of 6.2. These pH-induced changes of PE 607 -b-PLL 275 polymeric micelle size are unique and different to previous studies [25,27,33].

pH Responsivity of PE-b-PLL
As a kind of polyelectrolyte, PLL homopolymer has pH-responsive properties. Therefore, PE-b-PLL block copolymer is also expected to show pH responsivity. PE607-b-PLL275 was chosen as a representative sample to study pH responsivity. The effect of the pH value of the solution on the size of PE607-b-PLL275 was examined by DLS measurements. Figure 6A shows the pH-induced size changes on the hydrodynamic radius (Rh) of PE607b-PLL275 determined by DLS. Although a clear change of Rh with alternation of solution from basicity to acidity was observed, the unimodal size distributions (~0.14) still remained ( Figure 6B and Table S1). The Rh of PE607-b-PLL275 decreased with decreasing pH value from 9.0 (basicity) to 6.2 (near neutrality). When the pH value decreased from 6.2 to 1.5 (acidity), the Rh of PE607-b-PLL275 also decreased. Further decreasing the pH value from 1.5 to 0.5 (strong acidity) did not change the Rh. The biggest Rh was observed at near neutral solution (pH ≈ 7). TEM images (Figures 5 and 7) of polymeric micelles at different pH values also supported the pH-induced size change, and the biggest polymeric micelles were observed at pH of 6.2. These pH-induced changes of PE607-b-PLL275 polymeric micelle size are unique and different to previous studies [25,27,33].   Usually, the change of polymeric micelle size originates from the alteration in aggregation number. Furthermore, it is reported that PLL adopts different secondary conformational structures (α-helix, β-sheet, and coil) depending on the pH value of the solution, which can change micelle size [47][48][49]. Therefore, the effect of pH on secondary conformation of PLL block was investigated by UV-circular dichroism (CD) ( Figure 8). As shown in CD spectra of PE607-b-PLL275 at a pH of 9.0, a characteristic inflected curve with small negative maxima at 209 and 220 nm was observed, proving an α-helical conformation. In contrast, a positive maximum at 218 nm and a negative minimum at 197 nm were observed in CD curves at acidic conditions (pH = 6.2 and 3.5), confirming a coil conformation [33]. The CD spectra determined at different pH values had an isodichroistic point at 206 nm. These observations clearly prove that the conformation transition of PLL block is an alternation from a coil conformation at acidic conditions to an α-helical conformation at basic conditions without the presence of β-sheet [25]. Based on DLS, TEM, and CD analyses mentioned above, the pH-induced changes of micelle size are reasonably explained. When the solution condition is changed from basicity to neutrality, the conformation alteration of PLL segment is responsible for a decrease in micelle size. When the solution condition is changed from neutrality to acidity, the conformation of the PLL segment is the same, and the decrease of micelle size is attributed to the aggregation number of the polymer chain. A schematic illustration of selfassembly of the PE-b-PLL into spherical micelles in aqueous solution is shown in Scheme 2 [50][51][52]. In the polymeric micelles, hydrophobic PE segments are shrunken to form the micelle core in water, and hydrophilic PLL polymeric chains are located in the exterior of the micelles. PLL chains adopt coil conformation at acidic conditions and α-helical conformation at basic conditions. Usually, the change of polymeric micelle size originates from the alteration in aggregation number. Furthermore, it is reported that PLL adopts different secondary conformational structures (α-helix, β-sheet, and coil) depending on the pH value of the solution, which can change micelle size [47][48][49]. Therefore, the effect of pH on secondary conformation of PLL block was investigated by UV-circular dichroism (CD) ( Figure 8). As shown in CD spectra of PE 607 -b-PLL 275 at a pH of 9.0, a characteristic inflected curve with small negative maxima at 209 and 220 nm was observed, proving an α-helical conformation. In contrast, a positive maximum at 218 nm and a negative minimum at 197 nm were observed in CD curves at acidic conditions (pH = 6.2 and 3.5), confirming a coil conformation [33]. The CD spectra determined at different pH values had an isodichroistic point at 206 nm. These observations clearly prove that the conformation transition of PLL block is an alternation from a coil conformation at acidic conditions to an α-helical conformation at basic conditions without the presence of β-sheet [25]. Usually, the change of polymeric micelle size originates from the alteration in aggregation number. Furthermore, it is reported that PLL adopts different secondary conformational structures (α-helix, β-sheet, and coil) depending on the pH value of the solution, which can change micelle size [47][48][49]. Therefore, the effect of pH on secondary conformation of PLL block was investigated by UV-circular dichroism (CD) ( Figure 8). As shown in CD spectra of PE607-b-PLL275 at a pH of 9.0, a characteristic inflected curve with small negative maxima at 209 and 220 nm was observed, proving an α-helical conformation. In contrast, a positive maximum at 218 nm and a negative minimum at 197 nm were observed in CD curves at acidic conditions (pH = 6.2 and 3.5), confirming a coil conformation [33]. The CD spectra determined at different pH values had an isodichroistic point at 206 nm. These observations clearly prove that the conformation transition of PLL block is an alternation from a coil conformation at acidic conditions to an α-helical conformation at basic conditions without the presence of β-sheet [25]. Based on DLS, TEM, and CD analyses mentioned above, the pH-induced changes of micelle size are reasonably explained. When the solution condition is changed from basicity to neutrality, the conformation alteration of PLL segment is responsible for a decrease in micelle size. When the solution condition is changed from neutrality to acidity, the conformation of the PLL segment is the same, and the decrease of micelle size is attributed to the aggregation number of the polymer chain. A schematic illustration of selfassembly of the PE-b-PLL into spherical micelles in aqueous solution is shown in Scheme 2 [50][51][52]. In the polymeric micelles, hydrophobic PE segments are shrunken to form the micelle core in water, and hydrophilic PLL polymeric chains are located in the exterior of the micelles. PLL chains adopt coil conformation at acidic conditions and α-helical conformation at basic conditions. Based on DLS, TEM, and CD analyses mentioned above, the pH-induced changes of micelle size are reasonably explained. When the solution condition is changed from basicity to neutrality, the conformation alteration of PLL segment is responsible for a decrease in micelle size. When the solution condition is changed from neutrality to acidity, the conformation of the PLL segment is the same, and the decrease of micelle size is attributed to the aggregation number of the polymer chain. A schematic illustration of self-assembly of the PE-b-PLL into spherical micelles in aqueous solution is shown in Scheme 2 [50][51][52]. In the polymeric micelles, hydrophobic PE segments are shrunken to form the micelle core in water, and hydrophilic PLL polymeric chains are located in the exterior of the micelles. PLL chains adopt coil conformation at acidic conditions and α-helical conformation at basic conditions. Int. J. Mol. Sci. 2023, 24, x FOR PEER REVIEW 8 of 12 Scheme 2. The self-assembly of PE-b-PLL polymeric micelles in water.

Ionic Responsivity of PE-b-PLL
It is known that the addition of salt in the polypeptide solution often suppresses the pH responsivity because of the so-called "screening effect" of the charges on polypeptides [53]. Herein, NaCl was added into PE-b-PLL aqueous solutions to study the ionic effect on self-assembled polymeric micelles. As shown in Figure 6A (red line), the addition of NaCl into PE607-b-PLL275 solution led to a decrease in Rh at any pH value. The effect of salt concentration was further studied at pH = 1.5 because of coil conformation of PLL segments and nearly invariable micelle sizes at pH = 1.5. As shown in Figure 9, Rh markedly decreased with increasing NaCl concentration from 0 to 0.4 M, and then Rh remained nearly invariable by further increasing NaCl concentration from 0.4 to 1.0 M. This observation strongly indicates that electrostatic interactions are fully screened at NaCl concentration of 0.4 M. Generally, the presence of NaCl minifies the pH responsivity because of a screening of the electrostatic character.

Synthesis of PE-b-PZL Block Copolymers
A round-bottom Schlenk flask with a stirring bar was heated for 3 h to 150 °C under vacuum and then cooled to room temperature. The 0.2 g PE-COOCH( i Pr)NH2 macroinitiator was dissolved in 5 mL of dried CHCl3 and then injected into the Schlenk reactor under N2. The desired amount of Z-Lys-NCA monomer solution in dried CHCl3 was charged into the reactor, and the reaction was continuously stirred for 4 days at 25 °C. The polymeric product was isolated when the solution was poured into an excess of petroleum ether. The resultant polymers were collected and purified by filtration, which involved washing with petroleum ether several times and drying in vacuum at 40 °C to a constant weight.

Synthesis of PE-b-PLL Block Copolymers
A total of 6 mL of HBr/HAc solution was added into 8 mL solution of PE-b-PZL block copolymers (0.5 g) in CH3Cl. After 1 h, hydrolysis reactions were stopped and poured into 200 mL ether. The precipitated polymers were collected and washed with diethyl ether.

Ionic Responsivity of PE-b-PLL
It is known that the addition of salt in the polypeptide solution often suppresses the pH responsivity because of the so-called "screening effect" of the charges on polypeptides [53]. Herein, NaCl was added into PE-b-PLL aqueous solutions to study the ionic effect on self-assembled polymeric micelles. As shown in Figure 6A (red line), the addition of NaCl into PE 607 -b-PLL 275 solution led to a decrease in R h at any pH value. The effect of salt concentration was further studied at pH = 1.5 because of coil conformation of PLL segments and nearly invariable micelle sizes at pH = 1.5. As shown in Figure 9,

Ionic Responsivity of PE-b-PLL
It is known that the addition of salt in the polypeptide solution often suppresses the pH responsivity because of the so-called "screening effect" of the charges on polypeptides [53]. Herein, NaCl was added into PE-b-PLL aqueous solutions to study the ionic effect on self-assembled polymeric micelles. As shown in Figure 6A (red line), the addition of NaCl into PE607-b-PLL275 solution led to a decrease in Rh at any pH value. The effect of salt concentration was further studied at pH = 1.5 because of coil conformation of PLL segments and nearly invariable micelle sizes at pH = 1.5. As shown in Figure 9, Rh markedly decreased with increasing NaCl concentration from 0 to 0.4 M, and then Rh remained nearly invariable by further increasing NaCl concentration from 0.4 to 1.0 M. This observation strongly indicates that electrostatic interactions are fully screened at NaCl concentration of 0.4 M. Generally, the presence of NaCl minifies the pH responsivity because of a screening of the electrostatic character.

Synthesis of PE-b-PZL Block Copolymers
A round-bottom Schlenk flask with a stirring bar was heated for 3 h to 150 °C under vacuum and then cooled to room temperature. The 0.2 g PE-COOCH( i Pr)NH2 macroinitiator was dissolved in 5 mL of dried CHCl3 and then injected into the Schlenk reactor under N2. The desired amount of Z-Lys-NCA monomer solution in dried CHCl3 was charged into the reactor, and the reaction was continuously stirred for 4 days at 25 °C. The polymeric product was isolated when the solution was poured into an excess of petroleum ether. The resultant polymers were collected and purified by filtration, which involved washing with petroleum ether several times and drying in vacuum at 40 °C to a constant weight.

Synthesis of PE-b-PLL Block Copolymers
A total of 6 mL of HBr/HAc solution was added into 8 mL solution of PE-b-PZL block copolymers (0.5 g) in CH3Cl. After 1 h, hydrolysis reactions were stopped and poured into 200 mL ether. The precipitated polymers were collected and washed with diethyl ether.

Synthesis of PE-b-PZL Block Copolymers
A round-bottom Schlenk flask with a stirring bar was heated for 3 h to 150 • C under vacuum and then cooled to room temperature. The 0.2 g PE-COOCH( i Pr)NH 2 macroinitiator was dissolved in 5 mL of dried CHCl 3 and then injected into the Schlenk reactor under N 2 . The desired amount of Z-Lys-NCA monomer solution in dried CHCl 3 was charged into the reactor, and the reaction was continuously stirred for 4 days at 25 • C. The polymeric product was isolated when the solution was poured into an excess of petroleum ether. The resultant polymers were collected and purified by filtration, which involved washing with petroleum ether several times and drying in vacuum at 40 • C to a constant weight.

Synthesis of PE-b-PLL Block Copolymers
A total of 6 mL of HBr/HAc solution was added into 8 mL solution of PE-b-PZL block copolymers (0.5 g) in CH 3 Cl. After 1 h, hydrolysis reactions were stopped and poured into 200 mL ether. The precipitated polymers were collected and washed with diethyl ether. The crude polymers were further purified by extraction of water. The PE-b-PLL block copolymers were collected by removing water and drying in vacuum at 40 • C to a constant weight.

Preparation of the PE-b-PLL Polymeric Micelles
Amphiphilic PE-b-PLL solutions were prepared by direct dissolution in water at room temperature for 72 h. Aqueous solutions with various pH values and NaCl concentrations were prepared by dialysis of the solutions against water at various pH values and NaCl concentrations for 3 days. The aqueous solutions were allowed to equilibrate for at least 3 days under conditions of 25 • C before test.

Measurements
NMR spectra of polymers were carried out on a Bruker 500 MHz instrument (Bruker BioSpin, Billerica, Switzerland) in CDCl 3 or D 2 O. Gel permeation chromatography (GPC) analysis of the molecular weight and PDI of the PE sample at 150 • C was performed on a high-temperature chromatography, PL-GPC 220 instrument (Agilent, CA, USA) equipped with a triple detection array. GPC analysis of the molecular weight and PDI of PE-b-PZL copolymer sample was performed on a Waters GPC system (Waters, Middleton, WI USA) equipped with a refractive index detector at 40 • C. Fourier transform infrared (FT-IR) spectra were recorded on a Nicolet NEXUS-670 FTIR (Thermo Nicolet, Madison, WI, USA) spectrometer. Fluorescence spectra were recorded on a VARIAN Cary Eclipse fluorescence spectrophotometer (Varian, CA, USA) for CMC test. UV-circular dichroism (CD) analyses were performed at room temperature with a JASCO J 180 spectrometer (Jasco, Tokyo, Japan) employing quartz cells with 0.5 nm optical path length (185-250 nm). Dynamic light scattering (DLS) experiments were performed on a Malvern 300HSA Zetasizer instrument (Malvern Panalytical, Malvern, UK). Transmission electron microscopy (TEM) was performed on a TEM instrument (Philips TECNAI) (Philips-FEI, Eindhoven, The Netherlands) with an accelerating voltage of 120 kV. A negative staining technique was applied in observing self-assembly of PE-b-PLL amphiphiles.

Conclusions
In conclusion, we report the initial synthesis and characterization of well-defined amphiphilic PE-b-PLL block copolymers by combining nickel-catalyzed living ethylene polymerization with controlled ring-opening polymerization (ROP) of ε-Z-Lys-NCA and sequential post-functionalization. The prepared novel PE-b-PLL block copolymers are amphiphiles and can self-assemble into spherical micelles with a hydrophobic PE core in aqueous solution. The PLL segment endows PE-b-PLL block copolymer with pH and ionic responsivities in aqueous solution. The change of pH values leads to the conformational alteration of PLL from α-helix to coil, therefore changing micelle sizes. The presence of salt minifies the pH responsivity, and the electrostatic interactions are fully screened at NaCl concentration of 0.4 M. This kind of amphiphilic PE-b-PLL polymeric material shows potential for application in biomaterials.