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Dive into the research topics where Robert M. Lorenz is active.

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Featured researches published by Robert M. Lorenz.


Analytical Chemistry | 2009

Droplets for Ultrasmall-Volume Analysis

Daniel T. Chiu; Robert M. Lorenz; Gavin D. M. Jeffries

By using methods that permit the generation and manipulation of ultrasmall-volume droplets, researchers are pushing the boundaries of ultrasensitive chemical analyses. (To listen to a podcast about this feature, please go to the Analytical Chemistry Web site at pubs.acs.org/ancham.).


The Journal of Neuroscience | 2011

Protein Quantification at the Single Vesicle Level Reveals That a Subset of Synaptic Vesicle Proteins Are Trafficked with High Precision

Sarah A. Mutch; Patricia Kensel-Hammes; Jennifer C. Gadd; Bryant S. Fujimoto; Richard W. Allen; Perry G. Schiro; Robert M. Lorenz; Christopher L. Kuyper; Jason S. Kuo; Sandra M. Bajjalieh; Daniel T. Chiu

Protein sorting represents a potential point of regulation in neurotransmission because it dictates the protein composition of synaptic vesicles, the organelle that mediates transmitter release. Although the average number of most vesicle proteins has been estimated using bulk biochemical approaches (Takamori et al., 2006), no information exists on the intervesicle variability of protein number, and thus on the precision with which proteins are sorted to vesicles. To address this, we adapted a single molecule quantification approach (Mutch et al., 2007) and used it to quantify both the average number and variance of seven integral membrane proteins in brain synaptic vesicles. We report that four vesicle proteins, SV2, the proton ATPase, Vglut1, and synaptotagmin 1, showed little intervesicle variation in number, indicating they are sorted to vesicles with high precision. In contrast, the apparent number of VAMP2/synaptobrevin 2, synaptophysin, and synaptogyrin demonstrated significant intervesicle variability. These findings place constraints on models of protein function at the synapse and raise the possibility that changes in vesicle protein expression affect vesicle composition and functioning.


Analytica Chimica Acta | 2008

Simultaneous Generation of Multiple Aqueous Droplets in a Microfluidic Device

Robert M. Lorenz; Gina S. Fiorini; Gavin D. M. Jeffries; David S. W. Lim; Mingyan He; Daniel T. Chiu

This paper describes a microfluidic platform for the on-demand generation of multiple aqueous droplets, with varying chemical contents or chemical concentrations, for use in droplet based experiments. This generation technique was developed as a complement to existing techniques of continuous-flow (streaming) and discrete-droplet generation by enabling the formation of multiple discrete droplets simultaneously. Here sets of droplets with varying chemical contents can be generated without running the risk of cross-contamination due to the isolated nature of each supply inlet. The use of pressure pulses to generate droplets in parallel is described, and the effect of droplet size is examined in the context of flow rates and surfactant concentrations. To illustrate this technique, an array of different dye-containing droplets was generated, as well as a set of droplets that displayed a concentration gradient of a fluorescent dye.


Analytical Chemistry | 2010

Ultrasensitive and High-Throughput Fluorescence Analysis of Droplet Contents with Orthogonal Line Confocal Excitation

Gavin D. M. Jeffries; Robert M. Lorenz; Daniel T. Chiu

This paper describes a simple modification to traditional confocal fluorescence detection that greatly improves signal-to-noise (s/n) for the high-speed analysis of droplet streams. Rather than using the conventional epi geometry, illumination of the droplet was in the form of a line that is orthogonal to both the direction of flow and the light-collection objective. In contrast to the epi geometry where we observed high levels of scattering background from the droplets, we detected more than 10-fold less background (depending on the laser power used) when orthogonal-line-confocal illumination was used. We characterized this improvement using a standard microfluidic platform over a range of analyte concentrations and observed an improvement in limits of detection of greater than 10. Using this method, we were able to analyze picomolar concentrations of analytes contained within picoliter-volume droplets at a rate of greater than 350 droplets per second.


Lab on a Chip | 2007

Fabrication improvements for thermoset polyester (TPE) microfluidic devices

Gina S. Fiorini; Moonbin Yim; Gavin D. M. Jeffries; Perry G. Schiro; Sarah A. Mutch; Robert M. Lorenz; Daniel T. Chiu

Thermoset polyester (TPE) microfluidic devices were previously developed as an alternative to poly(dimethylsiloxane) (PDMS) devices, fabricated similarly by replica molding, yet offering stable surface properties and good chemical compatibility with some organics that are incompatible with PDMS. This paper describes a number of improvements in the fabrication of TPE chips. Specifically, we describe methods to form TPE devices with a thin bottom layer for use with high numerical aperture (NA) objectives for sensitive fluorescence detection and optical manipulation. We also describe plasma-bonding of TPE to glass to create hybrid TPE-glass devices. We further present a simple master-pretreatment method to replace our original technique that required the use of specialized equipment.


international quantum electronics conference | 2007

Controlled fusion of femtoliter-volume aqueous droplets using holographic optical tweezers

David McGloin; J. Buchanan; Daniel R. Burnham; Robert M. Lorenz; J.S. Edgar; Gavin D. M. Jeffries; Yiqiong Zhao; Daniel T. Chiu

This paper describes the use of Laguerre-Gaussian beams for the optical manipulation and fusion of single femtoliter-volume aqueous droplets, a technique developed to facilitate new applications in droplet microfluidics. In addition, this paper describes the possibility of extending this work by using more complex holographic fields generated by computer controlled spatial light modulators (i.e. dynamic holographic optical tweezers) which should lead to the control of larger arrays of droplets. Finally this paper discusses possible applications in the fields of digital microfluidics, with specific reference to the manipulation of cellular material within femtolitre test tubes.


Analytical Chemistry | 2005

Selective encapsulation of single cells and subcellular organelles into picoliter- and femtoliter-volume droplets.

Mingyan He; J. Scott Edgar; Gavin D. M. Jeffries; Robert M. Lorenz; and J. Patrick Shelby; Daniel T. Chiu


Accounts of Chemical Research | 2009

Chemistry and Biology in Femtoliter and Picoliter Volume Droplets

Daniel T. Chiu; Robert M. Lorenz


Analytical Chemistry | 2006

Microfluidic and optical systems for the on-demand generation and manipulation of single femtoliter-volume aqueous droplets.

Robert M. Lorenz; J. Scott Edgar; and Gavin D. M. Jeffries; Daniel T. Chiu


Archive | 2004

Method and device for biochemical detection and analysis of subcellular compartments from a single cell

Daniel T. Chiu; Bingyun Sun; James Patrick Shelby; John Scott Edgar; Gavin D. M. Jeffries; Robert M. Lorenz; Jason S. Kuo; Mingyan He; Peter B. Allen; Sarah A. Mutch; Christopher L. Kuyper; Gina S. Fiorini; David S. W. Lim

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Daniel T. Chiu

University of Washington

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Jason S. Kuo

University of Washington

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J. Scott Edgar

University of Washington

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Mingyan He

University of Washington

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Sarah A. Mutch

University of Washington

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