A heating-superfusion platform technology for the investigation of protein function in single cells.

Here, we report on a novel approach for the study of single-cell intracellular enzyme activity at various temperatures, utilizing a localized laser heating probe in combination with a freely positionable microfluidic perfusion device. Through directed exposure of individual cells to the pore-forming agent α-hemolysin, we have controlled the membrane permeability, enabling targeted delivery of the substrate. Mildly permeabilized cells were exposed to fluorogenic substrates to monitor the activity of intracellular enzymes, while adjusting the local temperature surrounding the target cells, using an infrared laser heating system. We generated quantitative estimates for the intracellular alkaline phosphatase activity at five different temperatures in different cell lines, constructing temperature-response curves of enzymatic activity at the single-cell level. Enzymatic activity was determined rapidly after cell permeation, generating five-point temperature-response curves within just 200 s.

[1]  O. Orwar,et al.  Probing enzymatic activity inside single cells. , 2013, Analytical chemistry.

[2]  Alar Ainla,et al.  An Optofluidic Temperature Probe , 2013, Sensors.

[3]  Jian-hui Jiang,et al.  Sensitive and Selective Label-free Alkaline Phosphatase Detection Based on DNA Hairpin Probe , 2012, Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.

[4]  Alar Ainla,et al.  A multifunctional pipette. , 2012, Lab on a chip.

[5]  N. Allbritton,et al.  Measuring enzyme activity in single cells. , 2011, Trends in biotechnology.

[6]  Daniel T Chiu,et al.  Protein Quantification at the Single Vesicle Level Reveals That a Subset of Synaptic Vesicle Proteins Are Trafficked with High Precision , 2011, The Journal of Neuroscience.

[7]  K. Murugan,et al.  Purification and kinetic characterization of the liverwort Pallavicinia lyelli (Hook.) S. Gray. cytosolic ascorbate peroxidase. , 2010, Plant physiology and biochemistry : PPB.

[8]  Ramon Grima,et al.  Investigating the robustness of the classical enzyme kinetic equations in small intracellular compartments , 2009, BMC Systems Biology.

[9]  R. Pringle,et al.  Spatial dynamics of nesting behavior: lizards shift microhabitats to construct nests with beneficial thermal properties. , 2009, Ecology.

[10]  A. Azhar,et al.  Partial purification and some properties of -amylase from Bacillus subtilis KIBGE-HAS , 2009 .

[11]  D. Weitz,et al.  Fluorescence-activated droplet sorting (FADS): efficient microfluidic cell sorting based on enzymatic activity. , 2009, Lab on a chip.

[12]  O. Reséndis-Antonio Filling Kinetic Gaps: Dynamic Modeling of Metabolism Where Detailed Kinetic Information Is Lacking , 2009, PloS one.

[13]  A. Grossman,et al.  Ancient recruitment by chromists of green algal genes encoding enzymes for carotenoid biosynthesis. , 2008, Molecular biology and evolution.

[14]  R. Schiffmann,et al.  Cellular and tissue distribution of intravenously administered agalsidase alfa. , 2007, Molecular genetics and metabolism.

[15]  Xiaoli Zhang,et al.  High-throughput single-cell analysis for enzyme activity without cytolysis. , 2006, Analytical chemistry.

[16]  O. Orwar,et al.  A chemical waveform synthesizer. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[17]  D. Chiu,et al.  Selective encapsulation of single cells and subcellular organelles into picoliter- and femtoliter-volume droplets. , 2005, Analytical chemistry.

[18]  Owe Orwar,et al.  A microfluidics approach to the problem of creating separate solution environments accessible from macroscopic volumes. , 2004, Analytical chemistry.

[19]  S. Schnell,et al.  Reaction kinetics in intracellular environments with macromolecular crowding: simulations and rate laws. , 2004, Progress in biophysics and molecular biology.

[20]  N. Allbritton,et al.  Measurement of kinase activation in single mammalian cells , 2000, Nature Biotechnology.

[21]  W. Telford,et al.  Detection of endogenous alkaline phosphatase activity in intact cells by flow cytometry using the fluorogenic ELF-97 phosphatase substrate. , 1999, Cytometry.

[22]  O Hindsgaul,et al.  Single cell studies of enzymatic hydrolysis of a tetramethylrhodamine labeled triglucoside in yeast. , 1999, Glycobiology.

[23]  J. Millán,et al.  Mammalian Alkaline Phosphatases Are Allosteric Enzymes* , 1997, The Journal of Biological Chemistry.

[24]  R. Huey,et al.  Evolution of thermal sensitivity of ectotherm performance. , 1989, Trends in ecology & evolution.

[25]  M. Boyer,et al.  The use of Histolyn CYL in an enzyme immunoassay to detect Histoplasma capsulatum antibodies. , 1983, Sabouraudia.

[26]  C. Wynn,et al.  The heterogeneous distribution of acid hydrolases within a homogeneous population of cultured mammalian cells. , 1973, Biochemical Journal.

[27]  M. Ayub,et al.  Production of organic acids by periplasmic enzymes present in free and immobilized cells of Zymomonas mobilis , 2012, Journal of Industrial Microbiology & Biotechnology.

[28]  F. Bruggeman,et al.  The nature of systems biology. , 2007, Trends in microbiology.

[29]  J. Millán Mammalian Alkaline Phosphatases: From Biology to Applications in Medicine and Biotechnology , 2006 .

[30]  J. Coleman,et al.  Structure and mechanism of alkaline phosphatase. , 1992, Annual review of biophysics and biomolecular structure.