TOPOFOLD, the designed modular biomolecular folds: polypeptide‐based molecular origami nanostructures following the footsteps of DNA. (4th September 2014)
- Record Type:
- Journal Article
- Title:
- TOPOFOLD, the designed modular biomolecular folds: polypeptide‐based molecular origami nanostructures following the footsteps of DNA. (4th September 2014)
- Main Title:
- TOPOFOLD, the designed modular biomolecular folds: polypeptide‐based molecular origami nanostructures following the footsteps of DNA
- Authors:
- Kočar, Vid
Božič Abram, Sabina
Doles, Tibor
Bašić, Nino
Gradišar, Helena
Pisanski, Tomaž
Jerala, Roman - Abstract:
- <abstract abstract-type="main" id="wnan1289-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="wnan1289-para-0001">Biopolymers, the essential components of life, are able to form many complex nanostructures, and proteins in particular are the material of choice for most cellular processes. Owing to numerous cooperative interactions, rational design of new protein folds remains extremely challenging. An alternative strategy is to design topofolds—nanostructures built from polypeptide arrays of interacting modules that define their topology. Over the course of the last several decades DNA has successfully been repurposed from its native role of information storage to a smart nanomaterial used for nanostructure self‐assembly of almost any shape, which is largely because of its programmable nature. Unfortunately, polypeptides do not possess the straightforward complementarity as do nucleic acids. However, a modular approach can nevertheless be used to assemble polypeptide nanostructures, as was recently demonstrated on a single‐chain polypeptide tetrahedron. This review focuses on the current state‐of‐the‐art in the field of topological polypeptide folds. It starts with a brief overview of the field of structural DNA and RNA nanotechnology, from which it draws parallels and possible directions of development for the emerging field of polypeptide‐based nanotechnology. The principles of topofold strategy and unique properties of such polypeptide nanostructures<abstract abstract-type="main" id="wnan1289-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="wnan1289-para-0001">Biopolymers, the essential components of life, are able to form many complex nanostructures, and proteins in particular are the material of choice for most cellular processes. Owing to numerous cooperative interactions, rational design of new protein folds remains extremely challenging. An alternative strategy is to design topofolds—nanostructures built from polypeptide arrays of interacting modules that define their topology. Over the course of the last several decades DNA has successfully been repurposed from its native role of information storage to a smart nanomaterial used for nanostructure self‐assembly of almost any shape, which is largely because of its programmable nature. Unfortunately, polypeptides do not possess the straightforward complementarity as do nucleic acids. However, a modular approach can nevertheless be used to assemble polypeptide nanostructures, as was recently demonstrated on a single‐chain polypeptide tetrahedron. This review focuses on the current state‐of‐the‐art in the field of topological polypeptide folds. It starts with a brief overview of the field of structural DNA and RNA nanotechnology, from which it draws parallels and possible directions of development for the emerging field of polypeptide‐based nanotechnology. The principles of topofold strategy and unique properties of such polypeptide nanostructures in comparison to native protein folds are discussed. Reasons for the apparent absence of such folds in nature are also examined. Physicochemical versatility of amino acid residues and cost‐effective production makes polypeptides an attractive platform for designed functional bionanomaterials. <italic>WIREs Nanomed Nanobiotechnol</italic> 2015, 7:218–237. doi: 10.1002/wnan.1289</p> <p id="wnan1289-para-0002">Conflict of interest: The authors have declared no conflicts of interest for this article.</p> <p>For further resources related to this article, please visit the <ext-link ext-link-type="uri" xlink:href="http://wires.wiley.com/remdoi.cgi?doi=10.1002/wnan.1289" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">WIREs website</ext-link>.</p> </abstract> … (more)
- Is Part Of:
- Wiley interdisciplinary reviews. Volume 7:Number 2(2015)
- Journal:
- Wiley interdisciplinary reviews
- Issue:
- Volume 7:Number 2(2015)
- Issue Display:
- Volume 7, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 7
- Issue:
- 2
- Issue Sort Value:
- 2015-0007-0002-0000
- Page Start:
- 218
- Page End:
- 237
- Publication Date:
- 2014-09-04
- Subjects:
- Nanomedicine -- Periodicals
Nanotechnology -- Periodicals
Biotechnology -- Periodicals
Ultrastructure (Biology) -- Periodicals
610.28 - Journal URLs:
- http://www3.interscience.wiley.com/journal/121524295/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/wnan.1289 ↗
- Languages:
- English
- ISSNs:
- 1939-5116
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3806.xml