A spectroscopic sensing platform for MARCKS protein monolayers

被引:1
作者
Klug, Joaquin [1 ,2 ]
Fernanda Torresan, Maria [3 ]
Lurgo, Florencia [3 ]
Borioli, Graciela [4 ]
Lacconi, Gabriela I. [3 ]
机构
[1] Univ Nacl Cuyo, CONICET, Padre Jorge Contreras 1300, RA-5500 Mendoza, Argentina
[2] Univ Nacl Cuyo, Fac Ciencias Exactas & Nat, Padre Jorge Contreras 1300, RA-5500 Mendoza, Argentina
[3] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Fis Quim, INFIQC CONICET, Ciudad Univ, RA-5000 Cordoba, Argentina
[4] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Quim Biol, CIQUIBIC CONICET, Ciudad Univ, RA-5000 Cordoba, Argentina
关键词
Silver nanoparticles electrodeposition; SERS active platforms; Intrinsically unstructured proteins; MARCKS; Langmuir-Blodgett monolayers; KINASE SUBSTRATE MARCKS; INTRINSICALLY DISORDERED PROTEINS; ENHANCED RAMAN-SCATTERING; MYRISTOYL-ELECTROSTATIC SWITCH; NATIVELY UNFOLDED PROTEINS; AMINO-ACIDS; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; UNSTRUCTURED PROTEINS; SI(111) SURFACES; LATERAL DOMAINS;
D O I
10.1016/j.jcis.2017.08.081
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We developed a highly sensitive silicon platform, suitable to assess the molecular organization of protein samples. Prototype platforms were obtained using different electrochemical protocols for the electrode position of Ag-nanoparticles onto the hydrogenated silicon surface. A platform with high Surface Enhanced Raman Scattering efficiency was selected based on the surface coverage and the number density of particles size distribution. The performance of the platform was determined by studying the interaction of Myristoylated Alanine-Rich C Kinase Substrate (MARCKS) protein with the substrate according to its molecular organization. The chemical and structural characteristics of MARCKS molecules were examined under two configurations: i) a disordered distribution given by a MARCKS solution drop deposited onto the platform and, ii) a compact monolayer transferred to the platform by the Langmuir-Blodgett method. Raman spectra show vibrational bands of Phenylalanine and Lysine residues specific for the protein effector domain, and evidence the presence of alpha helix structure in both configurations. Moreover, we distinguished the supramolecular order between the compact monolayer and random molecular distribution. The platforms containing Ag-nanoparticles are suitable for studies of protein structure and interactions, advancing a methodological strategy for our long term goal, which is to explore the interaction of proteins with model membranes. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:532 / 541
页数:10
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