TY - JOUR
T1 - Application of physicochemically modified silicon substrates as reverse-phase protein microarrays
AU - Nijdam, A. Jasper
AU - Zianni, Michael R.
AU - Herderick, Edward E.
AU - Cheng, Mark M.C.
AU - Prosperi, Jenifer R.
AU - Robertson, Fredika A.
AU - Petricoin, Emanuel F.
AU - Liotta, Lance A.
AU - Ferrari, Mauro
PY - 2009/3/6
Y1 - 2009/3/6
N2 - Physicochemically modified silicon substrates can provide a high quality alternative to nitrocellulose-oated glass slides for use in reverse-phase protein microarrays. Enhancement of protein microarray sensitivities is an important goal, especially because molecular targets within patient tissues exist in low abundance. The ideal array substrate has a high protein binding affinity and low intrinsic background signal. Silicon, which has low intrinsic autofluorescence, is being explored as a potential microarray surface. In a previous paper (Nijdam, A. J.; Cheng, M. M.-C.; Fedele, R.; Geho, D. H.; Herrmann, P.; Killian, K.; Espina, V.; Petricoin, E. F.; Liotta, L. A.; Ferrari, M. Physicochemically Modified Silicon as Substrate for Protein Microarrays. Biomaterials 2007, 28, 550-558), it is shown that physicochemical modification of silicon substrates increases the binding of protein to silicon to a level comparable with that of nitrocellulose. Here, we apply such substrates in a reverse-phase protein microarray setting in two model systems.
AB - Physicochemically modified silicon substrates can provide a high quality alternative to nitrocellulose-oated glass slides for use in reverse-phase protein microarrays. Enhancement of protein microarray sensitivities is an important goal, especially because molecular targets within patient tissues exist in low abundance. The ideal array substrate has a high protein binding affinity and low intrinsic background signal. Silicon, which has low intrinsic autofluorescence, is being explored as a potential microarray surface. In a previous paper (Nijdam, A. J.; Cheng, M. M.-C.; Fedele, R.; Geho, D. H.; Herrmann, P.; Killian, K.; Espina, V.; Petricoin, E. F.; Liotta, L. A.; Ferrari, M. Physicochemically Modified Silicon as Substrate for Protein Microarrays. Biomaterials 2007, 28, 550-558), it is shown that physicochemical modification of silicon substrates increases the binding of protein to silicon to a level comparable with that of nitrocellulose. Here, we apply such substrates in a reverse-phase protein microarray setting in two model systems.
KW - Nanotechnology
KW - Protein microarrays
KW - Proteomics
KW - Silicon
UR - http://www.scopus.com/inward/record.url?scp=65249133991&partnerID=8YFLogxK
U2 - 10.1021/pr800455y
DO - 10.1021/pr800455y
M3 - Article
C2 - 19170514
AN - SCOPUS:65249133991
SN - 1535-3893
VL - 8
SP - 1247
EP - 1254
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 3
ER -