Biospecific Recognition of Tethered Small Molecules Diluted in Self‐Assembled Monolayers
Biospecific Recognition of Tethered Small Molecules Diluted in Self‐Assembled Monolayers
复制标题
自组装单层稀释的束缚小分子的生物特异性识别
DOI:
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发表时间:
2008
期刊:
影响因子:
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通讯作者:
A. M. Andrews
中科院分区:
文献类型:
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作者:
M. Shuster;A. Vaish;Matthew E. Szapacs;M. E. Anderson;P. S. Weiss;A. M. Andrews
A model system for the capture of large biomolecule targets by small-molecule probes has been developed using a combination of insertion self-assembly and chemical functionalization. Key to selective molecular recognition of small molecules is the ability to tether these such that they are readily accessible for binding. This is particularly challenging because the tether alters a significant fraction of the probe molecule. It is also critical to space small-molecule probes so that they are dilute and exposed, rather than clustered via phase separation on capture surfaces, particularly when trying to bind large-molecule targets (e.g., proteins, nucleic acids). [1–5] Optimal dilution avoids the effects of steric hindrance [6–8] and multivalent non-specific interactions. Dilute surface coverage is also important to enable strategies to prevent nonspecific binding. We have developed a general method for addressing these problems [5,9–12] and apply these to surfaces functionalized with the small-molecule neurotransmitter serotonin (5-hydroxytryptamine; Fig. 1). Serotonin is covalently bound to tethers inserted at dilute coverage into pre-existing self-assembled monolayers (SAMs) bearing a molecular surface of oligo(ethylene glycol). We chose serotonin as our initial probe both because of its important roles as a neurotransmitter involved in anxiety and mood
影响因子:
7.4
作者:
Wegner, GJ;Lee, HJ;Corn, RM
通讯作者:
Corn, RM
影响因子:
7.4
作者:
Lahiri, J;Isaacs, L;Whitesides, GM
通讯作者:
Whitesides, GM