Modelling ligand-receptor interactions: from multivalent to Linker-mediated

Ligand-receptor interactions are not only fundamental principles of various biological processes but also provide a practical mechanism for self-assembly in various artificially engineered systems. In this thesis, we aim to offer an in-depth understanding of matters related to ligand-receptor intera...

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Main Author: Xia, Xiuyang
Other Authors: Massimo Pica Ciamarra
Format: Thesis-Doctor of Philosophy
Language:English
Published: Nanyang Technological University 2023
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Online Access:https://hdl.handle.net/10356/165288
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1652882023-04-04T02:58:00Z Modelling ligand-receptor interactions: from multivalent to Linker-mediated Xia, Xiuyang Massimo Pica Ciamarra Ni Ran School of Physical and Mathematical Sciences Massimo@ntu.edu.sg, r.ni@ntu.edu.sg Science::Physics::Atomic physics::Statistical physics Ligand-receptor interactions are not only fundamental principles of various biological processes but also provide a practical mechanism for self-assembly in various artificially engineered systems. In this thesis, we aim to offer an in-depth understanding of matters related to ligand-receptor interactions, particularly with a multivalent and linker-mediated nature. Firstly, we focus on the super-selectivity that emerges from the cooperativity of multivalent binding. We show that maximum selectivity occurs at intermediate binding energy and can be significantly larger than the weak binding limit for highly uniform receptor distributions. These results challenge the common belief in the biophysics community that weaker individual ligand-receptor binding always enhances the selectivity of multivalent nanoparticle binding. Secondly, we introduce the linker-mediated strategy and reveal non-trivial entropy-driven phase behavior in two valence-limited systems: linker-mediated DNA-coated colloids and linker-mediated vitrimers. We suggest a new axis for realizing programmable self-assembly of the DNA-coated colloidal system and provide an entropy-driven mechanism for crosslinking and thermo-gelling in vitrimers. Doctor of Philosophy 2023-03-23T01:59:45Z 2023-03-23T01:59:45Z 2023 Thesis-Doctor of Philosophy Xia, X. (2023). Modelling ligand-receptor interactions: from multivalent to Linker-mediated. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/165288 https://hdl.handle.net/10356/165288 10.32657/10356/165288 en This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0). application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Physics::Atomic physics::Statistical physics
spellingShingle Science::Physics::Atomic physics::Statistical physics
Xia, Xiuyang
Modelling ligand-receptor interactions: from multivalent to Linker-mediated
description Ligand-receptor interactions are not only fundamental principles of various biological processes but also provide a practical mechanism for self-assembly in various artificially engineered systems. In this thesis, we aim to offer an in-depth understanding of matters related to ligand-receptor interactions, particularly with a multivalent and linker-mediated nature. Firstly, we focus on the super-selectivity that emerges from the cooperativity of multivalent binding. We show that maximum selectivity occurs at intermediate binding energy and can be significantly larger than the weak binding limit for highly uniform receptor distributions. These results challenge the common belief in the biophysics community that weaker individual ligand-receptor binding always enhances the selectivity of multivalent nanoparticle binding. Secondly, we introduce the linker-mediated strategy and reveal non-trivial entropy-driven phase behavior in two valence-limited systems: linker-mediated DNA-coated colloids and linker-mediated vitrimers. We suggest a new axis for realizing programmable self-assembly of the DNA-coated colloidal system and provide an entropy-driven mechanism for crosslinking and thermo-gelling in vitrimers.
author2 Massimo Pica Ciamarra
author_facet Massimo Pica Ciamarra
Xia, Xiuyang
format Thesis-Doctor of Philosophy
author Xia, Xiuyang
author_sort Xia, Xiuyang
title Modelling ligand-receptor interactions: from multivalent to Linker-mediated
title_short Modelling ligand-receptor interactions: from multivalent to Linker-mediated
title_full Modelling ligand-receptor interactions: from multivalent to Linker-mediated
title_fullStr Modelling ligand-receptor interactions: from multivalent to Linker-mediated
title_full_unstemmed Modelling ligand-receptor interactions: from multivalent to Linker-mediated
title_sort modelling ligand-receptor interactions: from multivalent to linker-mediated
publisher Nanyang Technological University
publishDate 2023
url https://hdl.handle.net/10356/165288
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