Solid-phase synthesis of alkanethiols for the preparation of self-assembled monolayers

被引:18
作者
Derda, Ratmir [1 ]
Wherritt, Daniel J. [1 ]
Kiessling, Laura L. [1 ]
机构
[1] Univ Wisconsin, Dept Chem & Biochem, Madison, WI 53706 USA
关键词
D O I
10.1021/la701386v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-assembled monolayers (SAMs) of alkanethiols (ATs) on gold can be used to fabricate surfaces for nanoscience and biology. The chemical structure of the interface can be tailored simply by modifying the AT headgroup. To streamline access to different precursor ATs, we developed a general solid-phase synthetic route. A key feature of this route is the use of a modified resin containing an AT linker ("AT resin") because it minimizes purification steps. The precursor to the AT resin was prepared in five steps, and all of the synthetic intermediates are stable solids that can be purified by crystallization. Accordingly, the AT resin can be prepared on a multigram scale. The utility of the AT resin was evaluated by using it to generate a variety of ATs. For example, ATs presenting different types of integrin-binding ligands (linear and cyclic RGD derivatives) were prepared and used to form arrays of SAMs that support cell adhesion. Additionally, the AT resin also provides a starting point for the synthesis of ATs presenting reactive groups (e.g., an amine-reactive AT or a maleimide-containing alkanedisulfide) or protein immobilization tags (e.g., biotin-AT). Thus, our synthetic strategy provides a convenient and flexible means for the synthesis of the necessary building blocks for custom SAMs and SAM arrays.
引用
收藏
页码:11164 / 11167
页数:4
相关论文
共 44 条
[1]   In vitro and in vivo effects of a cyclic peptide with affinity for the αvβ3 integrin in human melanoma cells [J].
Allman, R ;
Cowburn, P ;
Mason, M .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (03) :410-422
[2]   Solid-phase oligosaccharide synthesis: Preparation of complex structures using a novel linker and different glycosylating agents [J].
Andrade, RB ;
Plante, OJ ;
Melean, LG ;
Seeberger, PH .
ORGANIC LETTERS, 1999, 1 (11) :1811-1814
[3]   FORMATION OF MONOLAYER FILMS BY THE SPONTANEOUS ASSEMBLY OF ORGANIC THIOLS FROM SOLUTION ONTO GOLD [J].
BAIN, CD ;
TROUGHTON, EB ;
TAO, YT ;
EVALL, J ;
WHITESIDES, GM ;
NUZZO, RG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (01) :321-335
[4]   Coassembly of amphiphiles with opposite peptide polarities into nanofibers [J].
Behanna, HA ;
Donners, JJJM ;
Gordon, AC ;
Stupp, SI .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (04) :1193-1200
[5]   COMPARISON OF ORGANIC MONOLAYERS ON POLYCRYSTALLINE GOLD SPONTANEOUSLY ASSEMBLED FROM SOLUTIONS CONTAINING DIALKYL DISULFIDES OR ALKENETHIOLS [J].
BIEBUYCK, HA ;
BIAN, CD ;
WHITESIDES, GM .
LANGMUIR, 1994, 10 (06) :1825-1831
[6]   A multistep chemical modification procedure to create DNA arrays on gold surfaces for the study of protein-DNA interactions with surface plasmon resonance imaging [J].
Brockman, JM ;
Frutos, AG ;
Corn, RM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (35) :8044-8051
[7]   Selective tumor cell targeting using low-affinity, multivalent interactions [J].
Carlson, Coby B. ;
Mowery, Patricia ;
Owen, Robert M. ;
Dykhuizen, Emily C. ;
Kiessling, Laura L. .
ACS CHEMICAL BIOLOGY, 2007, 2 (02) :119-127
[8]   Solid supported lipid bilayers: From biophysical studies to sensor design [J].
Castellana, Edward T. ;
Cremer, Paul S. .
SURFACE SCIENCE REPORTS, 2006, 61 (10) :429-444
[9]  
Chechik V, 2000, ADV MATER, V12, P1161, DOI 10.1002/1521-4095(200008)12:16<1161::AID-ADMA1161>3.0.CO
[10]  
2-C