School of Life and Environmental Sciences, Deakin University, Geelong, Victoria 3216, Australia.
Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, Ministry of Education; College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China.
Acc Chem Res. 2020 Mar 17;53(3):644-653. doi: 10.1021/acs.accounts.9b00612. Epub 2020 Feb 19.
Chirality is a fundamental property of a molecule, and the significant progress in chirality detection and quantification of a molecule has inspired major advances in various fields ranging from chemistry, biology, to biotechnology and pharmacology. Chiral molecules have identical molecular formulas, atom-to-atom linkages, and bonding distances, and as such they are difficult to distinguish both sensitively and selectively. Today, most new drugs and those under development are chiral, which requires technological developments in the separation and detection of chiral molecules. Therefore, rapid and facile methods to detect and discriminate chiral compounds are necessary to accelerate advances in many research fields. The challenges in analysis stem from the obvious fact that chiral molecules have the same physical properties. Although significant progress on the detection of enantiomeric composition has been achieved in the past decade, in order to fully realize the capacity of chiral molecular interrogation, highly sensitive and selective, portable, and easy-to-use detection remains challenging because of the limitation of conventional techniques.Soft nanoarchitectonics is a new concept for the fabrication of functional soft material systems through harmonization of various actions including atomic/molecular-level manipulation, chemical reactions, self-assembly and self-organization, and their modulation by external fields/stimuli. Soft nanoarchitectonics has been widely used as a key enabling technology for integrating predefined molecular functionalities including electrochemical, optical, catalytic, or biological properties into biosensing devices, which provides exciting opportunities to design, assemble, and fabricate tailored nanosystems to enable new sensing strategies for chiral molecules.In this Account, we aim to concisely discuss how these molecule-inspired soft nanoarchitectonics work for enantioselective sensing. We will first outline the basic principle and mechanistic insights of the soft nanoarchitectonics approach for enantioselective sensing, and then we will describe the new breakthroughs and trends in the area that have been most recently reported by our groups and others. There will also be a discussion on the merits of soft nanoarchitectonics based sensing in comparison to conventional analytical methods. Finally, with this Account, we hope to spark new chiral molecule sensing strategies by fundamentally understanding chiral recognition and engineering soft nanoarchitectonics with programmable structures and predictable sensing properties.
手性是分子的基本属性,分子手性检测和定量的显著进展激发了从化学、生物学到生物技术和药理学等各个领域的重大进展。手性分子具有相同的分子式、原子间连接和键长,因此它们既难以敏感又难以选择性地区分。如今,大多数新药物和正在开发的药物都是手性的,这需要在手性分子的分离和检测方面进行技术发展。因此,需要快速简便的方法来检测和区分手性化合物,以加速许多研究领域的进展。分析中的挑战源于手性分子具有相同物理性质这一明显事实。尽管在过去十年中对手性组成的检测取得了重大进展,但为了充分实现对手性分子的检测能力,仍然需要高度敏感和选择性、便携和易于使用的检测方法,因为受到传统技术的限制。软纳观学是通过协调原子/分子级操作、化学反应、自组装和自组织及其对外场/刺激的调制等各种作用来制造功能软材料系统的新概念。软纳观学已被广泛用作将电化学、光学、催化或生物性质等预定分子功能集成到生物传感设备中的关键使能技术,为设计、组装和制造定制的纳米系统以实现手性分子的新传感策略提供了令人兴奋的机会。在本述评中,我们旨在简要讨论这些受分子启发的软纳观学如何用于对映选择性传感。我们将首先概述软纳观学方法用于对映选择性传感的基本原理和机制见解,然后描述我们和其他小组最近报道的该领域的新突破和趋势。我们还将讨论基于软纳观学的传感与传统分析方法相比的优点。最后,通过对手性识别的基本理解和对手性分子的可编程结构和可预测传感特性的软纳观学工程,我们希望为新的手性分子传感策略提供新的思路。