Structuring peptide dendrimers through pH modulation and substrate binding

Luís C S Filipe, Sara R R Campos, Miguel Machuqueiro, Tamis Darbre, António M. Baptista

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Dendrimers are a family of ramified synthetic molecules. pH effects and electrostatic interactions are known to be crucial players to explain the conformational and functional behaviors observed in these systems. Nonetheless, to date, no computational study involving these systems has explicitly addressed the protonation equilibrium taking place at different pH values for dendrimers containing multiple ionizable sites. Herein, we present the results of constant-pH molecular dynamics simulations performed at several pH values for four peptide dendrimers of different generations (from one to four) composed of the same type of amino acids: histidines, serines, and diaminopropionic acid. These dendrimers are known to catalyze the hydrolysis of pyrene sulfonate esters. Constant-pH MD simulations in the presence of substrate molecules at the optimum pH for catalysis are also reported. The results show that first and second generation dendrimers are almost structurally unresponsive to pH variations. For third and fourth generation dendrimers, pH plays a structuring role, with markedly different behaviors being observed when passing from acidic to neutral pH. Protonation-conformation coupling effects influence several intramolecular interactions, which, in turn, modulate the shape and structure at the different pH values. The atypical and highly pH-dependent protonation profiles of some histidine residues are also investigated. The interactions between dendrimers and substrates restrict the conformational space available to the dendrimers and enforce conformational homogeneity. This structuring effect is a consequence of the dendrimer-substrate interactions which occur through stabilizing hydrogen bonds and ion pairs between the substrate sulfonate groups and the dendrimer residues. Our results provide original fundamental data contributing to the development of novel pH-modulated dendritic systems and the improvement of the existing ones.

Original languageEnglish
Pages (from-to)10138-10152
Number of pages15
JournalJournal of Physical Chemistry B
Volume120
Issue number38
DOIs
Publication statusPublished - 2 Sep 2016

Fingerprint

Dendrimers
dendrimers
Peptides
peptides
Modulation
modulation
Substrates
Protonation
Histidine
histidine
sulfonates
pH effects
Molecules
interactions
Pyrene
Coulomb interactions
Serine
Catalysis
pyrenes
Conformations

Cite this

Filipe, Luís C S ; Campos, Sara R R ; Machuqueiro, Miguel ; Darbre, Tamis ; Baptista, António M. / Structuring peptide dendrimers through pH modulation and substrate binding. In: Journal of Physical Chemistry B. 2016 ; Vol. 120, No. 38. pp. 10138-10152.
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Structuring peptide dendrimers through pH modulation and substrate binding. / Filipe, Luís C S; Campos, Sara R R; Machuqueiro, Miguel; Darbre, Tamis; Baptista, António M.

In: Journal of Physical Chemistry B, Vol. 120, No. 38, 02.09.2016, p. 10138-10152.

Research output: Contribution to journalArticle

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T1 - Structuring peptide dendrimers through pH modulation and substrate binding

AU - Filipe, Luís C S

AU - Campos, Sara R R

AU - Machuqueiro, Miguel

AU - Darbre, Tamis

AU - Baptista, António M.

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