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1 red on fibronectin than in cells cultured on polylysine.
2 s by recombinant human CKII is stimulated by polylysine.
3 lylysine and 0.22 +/- 0.12% for [99mTc] DTPA-polylysine.
4 bronectin but had no effect on attachment to polylysine.
5 A-man-PL and 0.13 +/- 0.08% for [99mTc] DTPA-polylysine.
6 asing protein (BPI or CAP57), protamine, and polylysine.
7  consisting of asialoglycoprotein coupled to polylysine.
8 r the MARCKS peptide or with the addition of polylysine.
9 y degraded protein, it bound to MDA-modified polylysine.
10 nder an electric field or in the presence of polylysine.
11 nk formation is observed with either AP-1 or polylysine.
12 approximately 15.0 MBq (99m)Tc-DTPA-succinyl-polylysine (2 microg; DTPA is diethylenetriaminepentaace
13 wly formulated alginate-glutamine degradable polylysine (A-GD-PLL) microcapsules.
14 aximal stimulation occurs at 10 microg/ml of polylysine, a concentration which has no effect on prote
15 report the crystallographic structure of the polylysine-actin-latrunculin A complex at 3.5-A resoluti
16  was 2.84 +/- 0.83% for [99mTc]DTPA-mannosyl-polylysine and 0.22 +/- 0.12% for [99mTc] DTPA-polylysin
17 epared with either short chain or long chain polylysine and a beta-galactosidase expression plasmid.
18 nificant increase in nonspecific adhesion to polylysine and BSA.
19                 Exogenous cationic polymers, polylysine and chitosan, can impart stimulatory activity
20 mplexes were formed between the mannosylated polylysine and oligonucleotides and added to the cells i
21 tions between the charged surface-associated polylysine and phosphatidylserine are sufficient to both
22                    In contrast, polycations (polylysine and polyethylenimine) and low-molecular-weigh
23 bosylation of not only polyarginine but also polylysine and polyhistidine, and ribosylation was inhib
24 hod uses inexpensive, commercially available polylysine and reusable glass plates.
25 ation of coacervate microdroplets comprising polylysine and short single strands of DNA generates mem
26 ediation of the DHP receptor (e.g. caffeine, polylysine, and peptide A), induced Ca(2+) release witho
27 kinetics of inhibition by the PIP2 scavenger polylysine, and the inhibition by the phosphatidylinosit
28 ed by cross-linking polyethylene glycol with polylysine around a salt-leached polylactic-co-glycolic
29 tor, LPDII, where DNA was first complexed to polylysine at a ratio of 1:0.75 (w/w) and then entrapped
30 rowth cones also caused actin bundle loss in polylysine-attached growth cones without loss of actin m
31 lent presentation of CGP77175A on a modified polylysine backbone (degree of polymerization = 1200; 50
32 th a peptide mimetope of dsDNA on a branched polylysine backbone (DWEYSVWLSN-MAP) induces a systemic
33 anocarriers (H-Dots) are composed of epsilon-polylysine backbone for charge variations, near-infrared
34 A3 or A6 peptides constructed on a branching polylysine backbone.
35 ions using two distinct peptides on branched polylysine backbones (multiple Ag peptide)-peptides.
36 sed binding, none of the amines that inhibit polylysine binding inhibits PC binding, suggesting that
37                                              Polylysine bound permanently to RG-II, precluding electr
38 ine, spermine, tRNA, DNA, polyglutamic acid, polylysine, bovine serum albumin, or histone did not rel
39 nic polyamino acids such as polyarginine and polylysine by fluorescence polarization.
40 s responsible for reversed galvanotropism on polylysine by growing neurons on tissue culture dishes w
41 ferences in electrostatic attraction between polylysine, carrageenan, and pectin.
42                         Polylysine-pectin or polylysine-carrageenan complexes were formed at mass rat
43 t high mass ratios, whereas those containing polylysine-carrageenan complexes were turbid and unstabl
44        Pectin did not strongly interact with polylysine-carrageenan complexes, whereas carrageenan di
45 (degree of polymerization = 1200; 50% of the polylysines carry the inhibitor) greatly enhanced in viv
46 the Ad type 7 fiber and retard DNA through a polylysine chain present at the C-terminus of this linke
47  have very high molecular weight (> 300,000) polylysine chains attached to them.
48  then fluorescently stained and stretched on polylysine-coated glass slides so that the positions of
49          The resulting cDNAs were arrayed on polylysine-coated glass slides.
50 fibronectin, laminin, or vitronectin but not polylysine-coated substrates.
51 ronectin but not to fibronectin, laminin, or polylysine-coated surfaces.
52 diated endocytosis of a ribozyme-transferrin-polylysine complex, specifically reduces both cellular F
53 in between those of the free DNA and the DNA.polylysine complex.
54 nd anti-IV in the form of asialoglycoprotein-polylysine complexes were administered to Huh7 cells, an
55 uptake showed a parallel relationship in the polylysine concentration range of 0-10 microM.
56  Under these conditions, the increase in the polylysine concentration resulted in the increase of bot
57 anodal turning were graded over the range of polylysine concentrations (0 = 0.1 < 1 < 10 = 100 microg
58 considered by growing neurites on a range of polylysine concentrations.
59                                          The polylysine conjugate was also longer acting than the mon
60 genes were complexed with asialoglycoprotein-polylysine conjugates, and 1 mg of the complexed DNA was
61 ine enkephalin, bradykinin, substance P, and polylysine-containing particles were determined with att
62             Dendrimers were synthesized on a polylysine core and bore either native GnRH (1, 2, and 5
63 a mixture of cytochrome b5, cytochrome c and polylysine, cytochrome b5 undergoes reversible electroch
64                           The synthesis of a polylysine dendron containing eight GdDOTA units conjuga
65 ide-modified alpha-ImI to an alkyne-modified polylysine dendron.
66 n techniques demonstrated that an adenovirus-polylysine-deoxyribonucleic acid (DNA) complex can be us
67 However, surprisingly, we found that epsilon-polylysine did not have a significant impact on lipid di
68 bstrates of gamma-PAK, such as histone 1 and polylysine, do not stimulate autophosphorylation or acti
69 hylenetriamine pentaacetic acid polymannosyl polylysine (DTPA-man-PL) was synthesized and tested for
70 In the presence of 1-5 mM Ca2+ (or 10 microM polylysine) ECaSt/PDI augmented the bovine pancreatic tr
71 antibody complexes and (99m)Tc-DTPA-succinyl-polylysine enabled in vivo visualization of very small a
72                                      epsilon-Polylysine (epsilon-PL) is a broad-spectrum antimicrobia
73 gements can be blocked by positively charged polylysine, further implicating electrostatic interactio
74                      With the most promising polylysine glycopolymer PL84(mimHNK-1)45 the inhibitory
75 ducing the 125I-ModOxLDL retention; however, polylysine had no effect.
76                               Both mucin and polylysine had pronounced influences on the particle siz
77  the presence of multiple Lys-Lys sequences, polylysines have tremendously enhanced affinity.
78 meric desorption rate k0 of polytyrosine and polylysine homopeptides from flat surfaces.
79 influenced by the cell type tested, although polylysine homopolymers demonstrate levels of internaliz
80 ected with other vectors by using adenovirus-polylysine in BAEC.
81 ed imidazole groups to the epsilon-amines of polylysine in varying mole ratios (73.5 mol % imidazole,
82 llapse, we cultured Helisoma growth cones on polylysine in which lamellipodial collapse was prevented
83 er levels of calcium loading (>150 nmol/mg), polylysine induced monophasic Ca2+ release curves (witho
84  that inhibits actin polymerization, arrests polylysine-induced nucleation at the level of an antipar
85 sing two different systems (C167PM actin and polylysine-induced polymerization of alpha-actin) show t
86                                              Polylysine inhibits elongation at both temperatures.
87 ortant implications for the incorporation of polylysine into food systems, particularly those contain
88                                              Polylysine is a cationic biopolymer with a strong antimi
89                                              Polylysine is added to prevent the normal decompaction o
90           A cationic polyamino acid, such as polylysine, is then added to the reaction mixture, where
91 GF2) that was first chemically conjugated to polylysine (K).
92 tinas were removed, dissociated, plated on a polylysine/laminin substrate, and maintained in vitro fo
93 or 8-day-old Long Evans rats and cultured on polylysine/laminin-coated coverslips in serum-free mediu
94     In addition, both lysine octapeptide and polylysine ligands were accessible for binding to hepari
95        In summary, a lectin-based intranasal polylysine-linked synthetic peptide vaccine was effectiv
96 by replacing its PHD with a polyhistidine or polylysine linker.
97                                          The polylysine modification and formation of ecotropic retro
98 ate that formation of amphotropic retrovirus polylysine molecular conjugates (aMMLV-PL) enhanced gene
99                                              Polylysine-molossin is a 31 amino acid synthetic peptide
100                  This peptide, when added to polylysine-molossin/DNA complexes at an optimal w/w rati
101           The addition of cationic lipids to polylysine-molossin/DNA conjugates gave excellent report
102  complexes at an optimal w/w ratio of 5:1:2 (polylysine-molossin/DNA/fusogenic peptide) resulted in 2
103 r to macromolecular acceptors (ubiquitin and polylysine) more strongly than transfer to small-molecul
104 aptotagmin interactions mediated by the C2 B polylysine motif are required to attain full synaptotagm
105                   Our analyses reveal that a polylysine motif at residues 189-192 confers an inhibito
106                                         This polylysine motif binds clathrin-adapter protein AP-2, ne
107                                    Thus, the polylysine motif functions after endocytosis and before
108                      The synaptotagmin 1 C2A polylysine motif functions independently of calcium-medi
109 and provide evidence that a highly conserved polylysine motif in this loop supports binding to negati
110                     Finally, mutation of the polylysine motif inhibits the Ca2+-independent ability o
111 We have demonstrated that incorporation of a polylysine motif into the pIX ectodomain results in a si
112   Together, our results demonstrate that the polylysine motif is required for efficient Ca2+-independ
113 uptake was unchanged in the mutants, and the polylysine motif mutant synaptotagmin was able to rescue
114                                              Polylysine motif mutants exhibited an apparent decreased
115 tagmin I (syt) transgenes harboring specific polylysine motif mutations into flies otherwise lacking
116 ic transmission, contains a highly conserved polylysine motif necessary for function.
117 endent interactions mediated through the C2A polylysine motif of synaptotagmin 1 function to modulate
118                  Addition of human beta2GP1, polylysine, native low-density lipoprotein, or apolipopr
119                          Neither adhesion to polylysine nor thrombin-induced aggregation caused simil
120                                      Neither polylysine nor two control peptides containing scrambled
121 18 DTPA and 82 mannosyl groups attached to a polylysine of 100 units ([99mTc]DTPA18-man82-PL100) were
122 he adhesion of cells to an adsorbed layer of polylysine on glass plates, followed by hypotonic lysis
123          We therefore examined the effect of polylysine on the digestion of corn oil-in-water emulsio
124 f labeled DNA the surfaces were treated with polylysine or 3-aminopropyl triethoxysilane or were coat
125 y blocking PI4K or using the PIP2 scavengers polylysine or bovine serum albumin reduced the incidence
126 comprising poly(ethylene oxide) and either a polylysine or polyester dendron were prepared and hydrop
127  an irrelevant plasmid bound to mannosylated polylysine or the expression plasmid bound to galactosyl
128                     The ability of beta2GP1, polylysine, or low-density lipoprotein to be a "cofactor
129 is triggered when polyphosphates bind to the polylysine patch in C2B domain and is stabilized by Mg(2
130                 We examined the stability of polylysine-pectin complexes in the presence of carrageen
131                         Solutions containing polylysine-pectin complexes were slightly turbid and rel
132 s, whereas carrageenan displaced pectin from polylysine-pectin complexes, which was attributed to dif
133                                              Polylysine-pectin or polylysine-carrageenan complexes we
134  either an integrin-binding RGD peptide or a polylysine peptide in the exposed HI loop.
135 an amide I band of ionized polyglutamate and polylysine, peptides which adopt a polyproline II helica
136 use the arginine-glycine-aspartame (RGD) and polylysine (pK7) motifs have been shown to enhance Ad5 i
137 at is condensed by electrostatic forces with polylysine (PL) covalently linked to streptavidin (binds
138 ximately 100 different complexes of DNA with polylysine (PL) or PL covalently attached to the glycopr
139 rus protein final sigma1, when conjugated to polylysine (PL), can bind the apical surface of M cells
140 mid DNA containing the gene of interest with polylysine (PL), PL linked to a replication-incompetent
141                               The effects of polylysine (PLL) and PLL-asialoorosomucoid (AsOR) on DNA
142 ay, however, where M1-4 lanes alternate with polylysine-(Plys)-only lanes, RGC axons from goldfish, z
143 on of polyplexes composed of plasmid DNA and polylysine (POL), a non-buffering polyamine, or the stro
144 nt produced in yeast and covalently bound to polylysine [poly(K)] to enable binding of DNA.
145                          Polycations such as polylysine, polyarginine, histone H1, histones H2A-H2B,
146 ng the ED(50) values of five macromolecules: polylysine, polyarginine, protamine, low-density lipopro
147       In contrast, less than 1 muM of a ChoP-polylysine polymer inhibited specifically the adhesion o
148 ltivalent nature of the MAG-IgM interaction, polylysine polymers of different sizes were substituted
149 bserved effects were highly dependent on the polylysine position in the mature domain.
150 ectrolytes consisting of cyanine dye pendant polylysines ranging in number of polymer repeat units (N
151 arboxyl-terminal methionine and the upstream polylysine region are important determinants for geranyl
152  cells confirmed the importance of the K-Ras polylysine region for microtubule binding, as deletion o
153                  These studies show that the polylysine region of K-Ras is critical for its interacti
154  of Ha-Ras and vice versa, we found that the polylysine region of K-Ras located immediately upstream
155 ible polycations consisting of histidine and polylysine residues (HIS RPCs) were evaluated for their
156 e expression plasmid bound to galactosylated polylysine resulted in no detectable transgene expressio
157 rted by polycations (neomycin, spermine, and polylysine) reversing the effect of PIP2 on TNP-ATP bind
158 netics observed for precursors with multiple polylysine segments support a model in which translocati
159 farnesyl modification and positively charged polylysine sequence.
160 ing of either eight consecutive lysines or a polylysine sequence.
161        The primary epsilon-amine terminus of polylysine served as a model for the cationic centers, w
162  with polycation poly(ethylene glycol) (PEG)-polylysine (single-coat (SC) nanozyme), we introduce for
163 erol product formed in the reaction binds to polylysine SPA beads, producing a signal that is measure
164                                Consequently, polylysine SPE/MALDI-MS targets offer a practical soluti
165 ing sequence of a variety of genes, encoding polylysine stretches that are important for protein func
166 l root ganglion (DRG) neurite outgrowth on a polylysine substrate and that asymmetric cGMP elevation
167                 Adhesion of macrophages to a polylysine substrate had no effect.
168 which transfected neurons were replated onto polylysine substrates suggest that activation of MEK is
169 be achieved using the antisense mannosylated polylysine system.
170 oximal external region (MPER), extended by a polylysine tail.
171                           Furthermore, these polylysine targets can capture over 60% of a protein fro
172 ration, for example, is some 50% larger with polylysine than with polyarginine.
173 lecular conjugate consisting of mannosylated polylysine that exploits endocytosis via the macrophage
174 ecular conjugate, consisting of mannosylated polylysine that exploits endocytosis via the macrophage
175      Ca2+ release from the SR was induced by polylysine (the ryanodine receptor-specific Ca2+ release
176 ography and wet etching and then coated with polylysine to facilitate cell adherence.
177 rylation does not occur when cells attach to polylysine, to which cells adhere in a nonspecific fashi
178 tail, resulting in C-terminal appendage of a polylysine tract and a terminally stalled ribosome.
179                  The neurons are cultured on polylysine-treated coverslips, which are suspended above
180 ace membranes of heat-killed neurons than on polylysine, underlining the importance of plasma membran
181 e due to the fluorescent dye, do not bind to polylysine unless hybridized to the negatively charged D
182 g lysine octapeptide, Ad vector displaying a polylysine was capable of recognizing cellular heparan s
183 ked DNA nor DNA complexed with unsubstituted polylysine was effective in gene transfer.
184 , and even with HIV nucleocapsid protein and polylysine, was unacceptable; the exception was a form o
185 es with differential adhesion to immobilized polylysine, we show that neuronal colony-forming precurs
186 ing enthalpies (polyhistidine, polyarginine, polylysine), weighted by numbers of such cationic groups
187        Nucleoids released in the presence of polylysine were easily processed and provided well-defin
188                          Adhesion to BSA and polylysine were not affected.
189  negatively charged, but neurites growing on polylysine, which is positively charged, turned toward t
190 ce with results obtained earlier for ionized polylysine, which suggest a high polyproline II propensi
191 f (111)In-diethylenetriaminepentaacetic acid-polylysine Z2D3-F(ab')(2), and SPECT imaging was perform

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