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Rational Design of Programmable Monodisperse Semi-Synthetic Protein Nanomaterials Containing Engineered Disulfide Functionality**

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TLDR
In this paper, a new chemical methodology for the construction of redox-sensitive protein assemblies using monodisperse facially amphiphilic protein-dendron bioconjugates is presented.
Abstract
The reversible nature of disulfide functionality has been exploited to design intelligent materials such as nanocapsules, micelles, vesicles, inorganic nanoparticles, peptide and nucleic acid nanodevices. Herein, we report a new chemical methodology for the construction redox-sensitive protein assemblies using monodisperse facially amphiphilic protein-dendron bioconjugates. The disulfide functionality is strategically placed between the dendron and protein domains. The custom designed bioconjugates self-assembled into nanoscopic objects of a defined size dictated by the nature of dendron domain. The stimuli-responsive behavior of the protein assemblies is demonstrated using a suitable redox trigger.

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Posted ContentDOI

Rational Design of Self-assembling Artificial Proteins Utilizing a Micelle-Assisted Protein Labeling Technology (MAPLabTech): Testing the Scope

TL;DR: In this article, the synthesis of self-assembling artificial proteins (SAPs) using micelle-assisted protein labeling technology (MAPLabTech) has been described by developing a chemical method for site-specific labeling of a surfaceexposed cysteine residue of globular proteins.
Journal ArticleDOI

Rational Design of Self‐Assembling Artificial Proteins Utilizing a Micelle‐Assisted Protein Labeling Technology (MAPLabTech): Testing the Scope **

TL;DR: The synthesis of novel SAPs are described by developing a chemical method for site‐specific labeling of a surface‐exposed cysteine residue of globular proteins and their systematic self‐assembly and disassembly studies using size‐exclusion chromatography are disclosed.
References
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Journal ArticleDOI

Strategies and challenges for the next generation of antibody–drug conjugates

TL;DR: Strategies to select the best target antigens as well as suitable cytotoxic drugs; the design of optimized linkers; the discovery of bioorthogonal conjugation chemistries; and toxicity issues are discussed.
Journal ArticleDOI

Drug delivery strategy utilizing conjugation via reversible disulfide linkages: role and site of cellular reducing activities

TL;DR: This review focuses on understanding where and how the disulfide bond in the bioconjugate is reduced upon contact with biological milieu, which affects delivery design and the interpretation of the delivery strategies.
Journal ArticleDOI

New directions in thermoresponsive polymers.

TL;DR: By highlighting recent examples of newly developed thermoresponsive polymer systems, it is hoped to promote the development of new generations of smart materials.
Journal ArticleDOI

The coming of age of de novo protein design

TL;DR: De novo protein design explores the full sequence space, guided by the physical principles that underlie protein folding, to design new functional proteins from the ground up to tackle current challenges in biomedicine and nanotechnology.
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