Shuffled lipidation pattern and degree of lipidation determines the membrane interaction behavior of a linear cationic membrane-active peptide
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Shuffled lipidation pattern and degree of lipidation determines the membrane interaction behavior of a linear cationic membrane-active peptide. / Hedegaard, Sofie Fogh; Bruhn, Dennis Skjoth; Khandelia, Himanshu; Cardenas, Marite; Nielsen, Hanne Morck.
I: Journal of Colloid and Interface Science, Bind 578, 2020, s. 584-597.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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T1 - Shuffled lipidation pattern and degree of lipidation determines the membrane interaction behavior of a linear cationic membrane-active peptide
AU - Hedegaard, Sofie Fogh
AU - Bruhn, Dennis Skjoth
AU - Khandelia, Himanshu
AU - Cardenas, Marite
AU - Nielsen, Hanne Morck
PY - 2020
Y1 - 2020
N2 - Hypothesis: Permeation of macromolecular drugs across biological plasma membranes is a major chal-lenge in drug delivery. Cationic cell-penetrating peptides (CPPs) are attractive functional excipient can-didates for the delivery of macromolecules across membrane barriers, due to their membrane translocating ability. The properties of CPPs can be tailored by lipidation, a promising approach to facil-itate enhanced membrane insertion, potentially promoting increased translocation of the CPP and cargo. Experiments: To explore the impact that site and degree of lipidation have on the membrane interaction of a cationic CPP, we designed and investigated CPP conjugates with one or two fatty acid chains. Findings: Compared to the parent CPP and the single-lipidated conjugates, the double-lipidated conjugate exhibited the most pronounced membrane perturbation effects, as measured by several biophysical tech-niques. The experimental findings were supported by molecular dynamics (MD) simulations, demon-strating that all CPP conjugates interacted with the membrane by insertion of the lipid chain(s) into the core of the bilayer. Moreover, membrane-thinning effects and induced membrane curvature were dis-played upon CPP interaction. Our results demonstrate that the impact exerted by the CPP on the mem-brane is notably affected by positioning and especially the degree of lipidation, which might influence the properties of CPPs as functional excipients. (c) 2020 Elsevier Inc. All rights reserved.
AB - Hypothesis: Permeation of macromolecular drugs across biological plasma membranes is a major chal-lenge in drug delivery. Cationic cell-penetrating peptides (CPPs) are attractive functional excipient can-didates for the delivery of macromolecules across membrane barriers, due to their membrane translocating ability. The properties of CPPs can be tailored by lipidation, a promising approach to facil-itate enhanced membrane insertion, potentially promoting increased translocation of the CPP and cargo. Experiments: To explore the impact that site and degree of lipidation have on the membrane interaction of a cationic CPP, we designed and investigated CPP conjugates with one or two fatty acid chains. Findings: Compared to the parent CPP and the single-lipidated conjugates, the double-lipidated conjugate exhibited the most pronounced membrane perturbation effects, as measured by several biophysical tech-niques. The experimental findings were supported by molecular dynamics (MD) simulations, demon-strating that all CPP conjugates interacted with the membrane by insertion of the lipid chain(s) into the core of the bilayer. Moreover, membrane-thinning effects and induced membrane curvature were dis-played upon CPP interaction. Our results demonstrate that the impact exerted by the CPP on the mem-brane is notably affected by positioning and especially the degree of lipidation, which might influence the properties of CPPs as functional excipients. (c) 2020 Elsevier Inc. All rights reserved.
KW - Cell-penetrating peptide
KW - Self-assembly
KW - Membrane thinning and curvature
KW - Molecular dynamics
KW - Isothermal titration calorimetry
KW - Quartz crystal microbalance with dissipation monitoring
KW - CELL-PENETRATING PEPTIDES
KW - COARSE-GRAINED MODEL
KW - MARTINI FORCE-FIELD
KW - SECONDARY STRUCTURE
KW - DOMAIN SEPARATION
KW - FATTY ACYLATION
KW - PANTP PEPTIDE
KW - RICH PEPTIDES
KW - DELIVERY
KW - MECHANISM
U2 - 10.1016/j.jcis.2020.05.121
DO - 10.1016/j.jcis.2020.05.121
M3 - Journal article
C2 - 32544630
VL - 578
SP - 584
EP - 597
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
SN - 0021-9797
ER -
ID: 253188929