Comparison of the Analysis Capabilities of Beckman Coulter MoFlo XDP and Becton Dickinson FACSAria I and II

Similar documents
Technical Bulletin. Guide for Using BD Cytometric Bead Array (CBA) Flex Sets with the BD Accuri C6 Flow Cytometer. Introduction

Manual Rosetta Calibration v

BD LSRFortessa X-20. Special Order Product. Designed for limited space and boundless potential

BD FC Beads 7-Color Kit

BD OneFlow Setup Beads

capabilities today. Flexibility for tomorrow.

BD LSRFortessa X-20. Special Order Product. Designed for limited space and boundless potential

quantiflash Calibration Light Source for Cytometry

Flow cytometer instrument set up

Acoustic resolution. photoacoustic Doppler velocimetry. in blood-mimicking fluids. Supplementary Information

Setup Procedure for Beckman Coulter CytoFLEX Flow Cytometer

ab Firefly Cytometer Setup Particles

Perform instrument startup and verification check following the manufacturer s recommendations.

Application Note (A13)

Perform instrument startup and verification check following the manufacturer s recommendations.

AbC Total Antibody Compensation Bead Kit

Supporting Information: An Optofluidic System with Integrated Microlens Arrays for Parallel Imaging Flow Cytometry

PMT Calibration in the XENON 1T Demonstrator. Abstract

Enhanced Sample Rate Mode Measurement Precision

Multiplexing as Essential Tool for Modern Biology

BD FC Beads 7-Color Kit

BD Trucount Controls IVD

MO BIO Laboratories, Inc Loker Ave. West, Carlsbad, CA 92010

Balancing Bandwidth and Bytes: Managing storage and transmission across a datacast network

Evaluation of Omega Mag-Bind TotalPure NGS Beads for DNA Size Selection

a Beckman Coulter Life Sciences: White Paper

Lab Report 3: Speckle Interferometry LIN PEI-YING, BAIG JOVERIA

577 nm: The Preferred Wavelength

In this lecture. System Model Power Penalty Analog transmission Digital transmission

Imaging Particle Analysis: The Importance of Image Quality

Optimizing the Movement of a Precision Piezoelectric Target Positioner. James Baase. Victor Senior High School Rochester, NY

Find Those Elusive ADC Sparkle Codes and Metastable States. by Walt Kester

Product Information. Introduction

A MONTE CARLO CODE FOR SIMULATION OF PULSE PILE-UP SPECTRAL DISTORTION IN PULSE-HEIGHT MEASUREMENT

LEGENDplex. Please read the entire manual before running the assay. BioLegend.com. Please read the entire manual before running the assay.

Additional reagents and materials that are not supplied

Franck-Hertz measurement of the excitation energy of mercury

Basic Microprocessor Interfacing Trainer Lab Manual

Teaching fiber-optic communications in engineering technology programs by virtual collaboration with industry

IonWorks Barracuda Plus Automated Patch Clamp System. Unmatched performance for automated electrophysiology.

Ultra-reliable AlGaInAs Diode Laser Technology Impacts the Industrial Laser Marketplace Based on an article appearing in Laser Focus World, March 2003

The Importance of Data Converter Static Specifications Don't Lose Sight of the Basics! by Walt Kester

Developing a novel method for the screening of fungal germinated spores using hydrogel microencapsulation and large particle flow cytometry.

LEGENDplex. Cat. No Human Proinflammatory Chemokine Panel (13-plex) Please read the entire manual before running the assay.

LEGENDplex. Cat. No Human Cytokine Panel 2 (13-plex) Please read the entire manual before running the assay.

Enabling Legendary Discovery. LEGENDplex. LEGENDplex. Mul -Analyte Flow Assay Kit. Please read the entire manual before running the assay.

Evaluation of High Intensity Discharge Automotive Forward Lighting

Franck-Hertz measurement of the excitation energy of mercury

LEGENDplex. Cat. No Human CD8/NK Panel (13-plex ) Please read the entire manual before running the assay.

COMPENSATION: AN INTRODUCTION

Chapter 11. Sampling Distributions. BPS - 5th Ed. Chapter 11 1

LOABeads MagSep 15/50 LOABeads MagSep 500

Application Note 106 IP2 Measurements of Wideband Amplifiers v1.0

Smarter oil and gas exploration with IBM

An Evaluation of Artifact Calibration in the 5700A Multifunction Calibrator

AdnaTest OvarianCancer-2 Select

Procedure & Checklist - Greater Than 10 kb Template Preparation Using AMPure PB Beads

Ultrasensitive LC MS/MS: Agilent 6470 and 6495 LC-QQQ

TECHNICAL PAPER. Smarter Sensors reduce costs for Motion Control Integrators. David Edeal. Introduction

NEW LASER ULTRASONIC INTERFEROMETER FOR INDUSTRIAL APPLICATIONS B.Pouet and S.Breugnot Bossa Nova Technologies; Venice, CA, USA

Introduction. APPLICATION NOTE 3981 HFTA-15.0 Thermistor Networks and Genetics. By: Craig K. Lyon, Strategic Applications Engineer

Positive Pixel Count Algorithm. User s Guide

Procedure and Checklist - 20 kb Template Preparation Using BluePippin Size-Selection System

DIGITAL Radio Mondiale (DRM) is a new

Electronic Systems - B1 23/04/ /04/ SisElnB DDC. Chapter 2

ELECTRONIC SYSTEMS. Introduction. B1 - Sensors and actuators. Introduction

ECE 317 Laboratory #1 Force Sensitive Resistors

OPTICAL BACKSCATTER REFLECTOMETER TM (Model OBR 5T-50)

WIRELESS 20/20. Twin-Beam Antenna. A Cost Effective Way to Double LTE Site Capacity

LA-950 Laser Diffraction Analyzer

Statistical Analysis of Modern Communication Signals

Analysis and Decomposition of Duty Cycle Distortion from Multiple Sources

Bias errors in PIV: the pixel locking effect revisited.

Multi-channel imaging cytometry with a single detector

potentiostat/galvanostat/impedance analyser

Nonuniform multi level crossing for signal reconstruction

Confidently Assess Risk Using Public Records Data with Scalable Automated Linking Technology (SALT)

Lecture Fundamentals of Data and signals

HF Upgrade Studies: Characterization of Photo-Multiplier Tubes

QUANTOF. High-resolution, accurate mass, quantitative time-of-flight MS technology

AdnaTest EMT-1/StemCellSelect

Chapter Two. Fundamentals of Data and Signals. Data Communications and Computer Networks: A Business User's Approach Seventh Edition

Simulation comparisons of monitoring strategies in narrow bandpass filters and antireflection coatings

BoTest Matrix E Botulinum Neurotoxin Detection Kit Protocol

CHAPTER 6 INTRODUCTION TO SYSTEM IDENTIFICATION

Using Iterative Automation in Utility Analytics

Beyond beads. Develop high performance assays, fast

Texture characterization in DIRSIG

Characterization of L5 Receiver Performance Using Digital Pulse Blanking

Comparison of FRD (Focal Ratio Degradation) for Optical Fibres with Different Core Sizes By Neil Barrie

Convention e-brief 310

Some Parameter Estimators in the Generalized Pareto Model and their Inconsistency with Observed Data

Novel techniques for refractive index determination of single nanoparticles in suspension

Chapter 3 Data and Signals 3.1

Phased Array Velocity Sensor Operational Advantages and Data Analysis

Experimental protocol PIPE

Procedure & Checklist - 10 kb Template Preparation and Sequencing (with Low-Input DNA)

The Best Way to Get the Right Answers... is in a Flash

Introduction to BioImage Analysis

DEVELOPMENT OF A DIGITAL TERRESTRIAL FRONT END

Transcription:

Comparison of the Analysis Capabilities of Beckman Coulter MoFlo XDP and Becton Dickinson FACSAria I and II Dr. Carley Ross, Angela Vandergaw, Katherine Carr, Karen Helm Flow Cytometry Business Center, Beckman Coulter, Inc., Fort Collins, CO, University of Colorado Cancer Center, Aurora, CO Abstract The speed at which a flow cytometer can accurately and efficiently measure samples becomes more significant as flow cytometry expands to more demanding applications and experiments. Therefore, a standard, repeatable, singlet bead assay was developed to compare the analytical capabilities of the Beckman Coulter MoFlo XDP and the Becton Dickinson FACSAria I and II. The Aria II, while capable of bead analysis at 65K events per second (EPS), lost data ranging from 20% of expected events at 20K EPS to 75% of expected events at 65K EPS. MoFlo XDP produced no measurable data loss at rates up to 80K EPS and relatively minimal loss (20%) at 140K EPS. The XDP data was confirmed by third-party analysis. The results of the comparison show that the MoFlo XDP measures more events, and accurately analyzes events four to five times faster than Aria I and II. Introduction Scientific and clinical researchers working in flow cytometry today experience increasing demands to perform experiments and applications that involve high throughput, rare-event analysis and detailed immunophenotyping. Analysis of rare populations, such as stem cells, demands that the majority of the sample is analyzed, and that events are not lost due to instrument limitations. Equally important in rare-event analysis is the need for results that provide high confidence in the statistical distribution of data. Furthermore, rare-event analysis and detailed immunophenotyping can be time consuming. Therefore, samples must be run rapidly in order to preserve the quality of time-sensitive material, and to make the most of laboratory resources. Beckman Coulter (BCI) and Becton Dickinson (BDIS) offer multi-use flow cytometry sorters that, according to specification sheets, can analyze up to 70K EPS with more than nine parameters enabled. The amount of data obtained from a sample varies greatly between instrument platforms. One hypothesis for the cause of the discrepancy in instrument performance is that the platforms have different electronic acquisition structures and sample delivery methods. MoFlo XDP (BCI) uses a narrow pulse width to detect events (Figure 5) and delivers sample through jet-in-air. The Aria (BDIS) uses a wider pulse width as well as a pulse Figure 1. Expected EPS The black line represents the calculated expected EPS values. The discrepancy between the expected and observed events per second is due to the lost events, defined as the events that were expected, but missed and never recorded. Due to the narrower pulse width, the MoFlo XDP missed very few events until speeds reached over 100K EPS, whereas the Aria began to lose events at an acquisition speed of 20K EPS and was unable to reach rates above 65K EPS. 0005218 Rev. A

width extension, and delivers sample through a cuvette. Prior to this study, the theoretical extent to which the Aria pulse width and window extension affect sample measurements had been studied by Dan Fox 1 but not demonstrated empirically. This study was designed to quantify how the differences between XDP and Aria electronics and sample delivery affect speed and sample analysis. Before examining the data it is important to understand the concepts of pulse width, lost events, and hard aborts. Pulse width is defined as time elapsed from the point at which an event signal crosses a set threshold and then falls below the threshold. The wider the pulse width, the longer the interval of elapsed time. Events per second (EPS) is defined as the total number of threshold breaches per second, including aborts. Lost events are defined as events that were expected, but never detected. Hard aborts (or electronic aborts for Aria) are defined as events that were detected, but the electronics could not discern if the signal represented one or more events. Theoretically, increased pulse width should cause an instrument to detect fewer distinct events. The effect should be amplified as acquisition speed increases because events will arrive at the interrogation point closer together. Considering the theoretical potential of Figure 2. Hard Abort Rate Bead assay samples were run at different speeds while the hard (electronic) abort rate was measured. During analysis, the MoFlo XDP produced no measured hard aborts. The Aria I experienced approximately 9K hard aborts per second at 50K EPS, and the Aria II experienced approximately 14K hard aborts per second at 65K EPS. This translates into a 20% sample loss at the highest Aria speed. lost and aborted data due to pulse width, it is important to quantify which instrument produces better results when samples are analyzed at top speeds. Therefore, an iterative and reproducible singlet bead assay was created to test the acquisition speed versus sample yield on the XDP and the Aria. Figure 3 A. MoFlo XDP Data Loss The MoFlo XDP had 0% hard aborts and lost events until acquisition speeds reached above 100K EPS. B. Aria II Data Loss. After 20K EPS, the Aria II lost incrementally more data as the speed increased until it reached 75% data loss at 65K EPS. Page 2

Results The comparison of analytical capabilities between the XDP and the Aria demonstrated that the XDP measures more events with fewer aborts, and more accurately analyzes events at rates up to five times faster than the Aria. A total of 15 sample concentrations were analyzed on the XDP and the Aria. The effect of pulse width and window extension can be seen in the differences between captured events per second (Figure 1) and the hard aborts for each platform (Figure 2). Speed of acquisition: XDP is faster and obtains more data per sample. The XDP and the Aria were set at an identical pressure differential to define stream width for both instruments. Theoretically, if the stream width is the same, the two instruments should measure the same number of events per second as the sample concentrations increase. Each experiment was executed in triplicate and the results are displayed with corresponding error bars. Minimal variation in the data points from multiple iterations of the experiment demonstrates the robust nature of the bead assay as a repeatable, dependable measure of analysis. Aria loses 38% more data than XDP at high speeds and high sample concentrations. As shown in Figure 1, the comparison between expected and observed EPS on both platforms emphasizes the Aria s loss of event detection. Throughout the bead assay, the EPS recorded by the XDP matched the expected EPS up to approximately 100K EPS. In contrast, the Aria began to lose events at 20K EPS and, regardless of expected events, could detect no more than 65K EPS (Figure 1). Both systems produced lost events. However, the Aria encountered a much earlier loss at 20K EPS, reaching a 50% data loss at 65K EPS. Hard Aborts: Aria aborts up to 20% of data, XDP aborts 0% of data. The XDP produced no hard aborts at processing speeds up to 110K EPS (Figure 3A). However, the Aria had an incremental increase in the hard abort rate starting at 3K EPS producing 10 hard aborts per second when a 2 µs window extension was used as recommended in the BD FACSAria User s Guide 2. When the Aria reached a processing speed of 65K EPS, the hard abort rate increased to 14K, a 20% data loss (Figure 3B). Total Data Analyzed: Aria loses up to 75% of data, XDP loses 20% of data at highest speeds and sample concentrations. Total sample recovery was calculated by combining the lost events and hard aborts for the XDP and the Aria. The XDP (Figure 3A) recovered its entire sample until the speed reached 80-100K EPS. The Aria recovered only 25% of the sample at 65K EPS but began losing events at 20K EPS (Figure 3B). Instrument differences can also be seen in Figure 4 where the total data analyzed is plotted for each platform. Again, the XDP analyzed most of its sample, whereas the Aria, at higher speeds, lost up to 75%. Figure 4. Comparison of the Total Data Analyzed The MoFlo XDP produced few aborts until the acquisition speed reached 100K EPS. The Aria (I and II) lost data beginning at 20K EPS and plateaued at 65K EPS with the total sample analyzed decreasing to 25%. Discussion The bead assay was developed with singlet beads as an effective way to measure both the hard aborts and lost events produced by the XDP and the Aria. With the same samples used on each instrument, and the expected events in the samples already established, events lost during analysis could be accurately determined. Theoretical calculations (Fox 1 ) indicate that the pulse width of the Aria is almost five times longer (3.96 µs versus XDP 0.82 µs) for a 13 µm cell. Increased pulse width is detrimental to the determination of singlet versus doublet events. A shorter pulse distinguishes each event separately giving a more accurate measurement of event count and speed. Figure 5 illustrates the calculated theoretical pulse width (Fox 1 ) on the XDP and the Aria for random events disregarding hydrodynamic focusing. Events that are well-separated do not exhibit a difference in EPS or hard abort rate during analysis (Figure 5 event A). If the events are closer together (B and C), the size of the pulse width Page 3

signal changes the data obtained. The XDP analyzes (B and C) events as two discrete measurements. On the other hand, the Aria with the increased pulse width does not distinguish two events, but instead produces one distorted signal (brighter signal, wider scatter) and ignores event C. Event C is not counted by the electronics and therefore is lost. During multi-laser analysis, adjustments to pulse width must be made to account for changes in particle velocity. The XDP uses a sliding-window system to detect events across all three laser detection pinholes. This sliding window maintains pulse width integrity while permitting precise measurements through all laser lines. In contrast, the BD FACSAria User s Guide 2 recommends that users implement a fixed 2 µs window extension when performing multi-laser analysis. This time added to the threshold is intended to help detect the signal from all laser lines. In theoretical calculations, the resulting pulse width increases from 3.96 µs to 5.96 µs for a 13 µm cell, making the pulse width seven times longer than the XDP pulse width. This difference is noticeable when events (B and C) and (D and E) pass through the stream and result in increased pulse width on the Aria. This causes hard aborts for (D Figure 5. MoFlo XDP vs. Aria Pulse Width Events that are well-separated do not exhibit a difference in EPS or hard abort rate during analysis (Figure 5 event A). If the events are closer together (B and C), the size of the pulse width signal changes the data obtained. The XDP analyzes (B and C) events as two discrete measurements. On the other hand, the Aria with the longer pulse width does not distinguish two events, but instead produces one distorted signal (brighter signal, wider scatter) and ignores event C. Event C is not counted by the electronics and therefore is lost. During multi-laser analysis, adjustments to pulse width must be made to account for changes in particle velocity. The XDP uses a sliding-window system to detect events across all three laser detection pinholes. This sliding window maintains pulse width integrity while permitting precise measurements through all laser lines. In contrast, the BD FACSAria User s Guide 2 recommends that users implement a fixed 2 µs window extension when performing multi-laser analysis. This difference is noticeable when events (B and C) and (D and E) pass through the stream and result in increased pulse width on the Aria. This causes hard aborts for (D and E) events, and is perhaps why the signal from event (B-C) is distorted and event C is lost. The deciding factor in successful multiple laser data acquisition is the pulse width window, sliding or fixed. During multiple laser acquisition the XDP loses 0 events, whereas the Aria possibly aborts 3 and ignores 1 event out of 5. Page 4

and E) events, and is why the signal from event (B-C) is distorted and event C is lost. The deciding factor in successful multiple laser data acquisition is the pulse width window, sliding or fixed. During multiple laser acquisition the XDP loses no events, whereas the Aria possibly aborts 3 and ignores 1 event out of 5. Pulse Width: Wider means more data lost. As previously discussed, the increased pulse width used by the Aria would clearly impact data analyzed. The disparity between expected and observed EPS could be explained by the lost event which occurs when two events are too close together to be measured and are taken as one event (Figure 1, Figure 5). The Aria loses 50% of its sample to lost events at 65K EPS, whereas the XDP only begins to have the same problem at speeds of 80K EPS (4% loss) up to 140K EPS (21% loss). The XDP s narrower pulse width measures more sample and more efficiently resolves doublets. Aria window extension: Increases pulse width and creates more aborts. The variation in event acquisition during multilaser analysis adds additional data loss for the Aria. The Aria s fixed window extension increases the pulse width and therefore causes more aborts (20% hard aborts at 65K EPS). Aria users may adjust the window extension, but sample resolution may suffer. In contrast, the XDP s sliding window keeps the pulse width narrow, thereby producing no aborts. Conclusion In conclusion, the Aria, while capable of analyzing beads at 65K EPS, produced data loss ranging from 20% at low speeds to 75% at 65K EPS. However, the MoFlo XDP had 0% data loss at rates up to 80K EPS and relatively minimal loss (20%) at rates twice the specified EPS limit. Materials and Methods Sample Preparation Samples were prepared with 7.06 µm Bangs Laboratory (Fishers, IN) carboxylated beads with a >95% singlet status, 10% w/v beads (4.90 x10 8 beads per ml). The primary sample was created with 2.0 ml of beads and 800 µl of DI H 2 O (+0.01% NP40) in a 5 ml polystyrene tube and then 2.0 ml of the dilution was used in succession until the 15th tube was reached in a dilution series. Samples were kept at 4ºC (39 F) until used within a 24-hour period. Flow Cytometry Both the MoFlo XDP and the Aria I and II were set up as described in their instrumentation manuals 2,3 with calibration done according to specifications. The threshold setting was also kept constant, and the differential pressure was set to 3000 EPS ± 100 for the lowest dilution sample. This ensured that both instruments had the same stream width. Acquisition Beads were analyzed on two parameters, FSC- Height versus SSC-Height with the voltages set within the accepted PMT voltages for maximum signal/minimum noise. All other parameters were removed from capture to reduce computer processor requirements. A minimum of 2 million events per sample were recorded. Samples were run on both instruments concurrently, using the same bead dilution tube consecutively to remove any variability due to sample preparation. Each experiment was done in triplicate on all instruments. Data was recorded on threshold count, events per second, electronic (hard aborts), and acquisition time (seconds). Calculations 1. Expected events per second = (Starting EPS/dilution factor) 2. Calculated events per second = (Event count/ analysis time) 3. Hard abort rate = (Hard aborts/acquisition time) 4. Percentage of lost events = (Expected EPS - actual EPS)/expected EPS 5. Percentage of hard aborts = Abort count/event count 6. Percentage of total sample recovered = 100% - (100% - Percentage lost events) + (100% - Percentage hard aborts) References 1. Fox, D. Analysis of Electronic Yield. available on coulterflow.com, June 2007. 2. BD FACSAria User s Guide, 2003, available on bdbiosciences.com. 3. MoFlo XDP Instructions for Use, 2009, available on coulterflow.com Copyright The Beckman Coulter logo and MoFlo XDP are trademarks of Beckman Coulter, Inc. All other trademarks are registered trademarks of their respective holders. Acknowledgements I would like to thank all of the collaborators for the third party data, Dan Fox and Charley Bay for their expertise in electronic acquisition, Dr. Alan Dean for reviewing the material, Marni Crowell for editing and layout, and all BCI staff at Fort Collins for their help and support. Page 5

Customer Impact This study demonstrates that hard aborts and lost events, constitute an important difference between the MoFlo XDP and the Aria I and II. By choosing a MoFlo XDP, the user is expected to gain the following benefits: MoFlo XDP... Rationale Obtains more information from each sample during analysis. Very few events are lost. Serves more customers in core labs. Samples can be run faster (4-5X faster) than Aria I and II. Captures rare events in sample populations quickly. Reduces potential for missing rare populations because few events are aborted. Maintains cell viability. Sample run time is reduced, preventing cell degradation of time sensitive samples. Heightens customer confidence. Very little data is lost (even at high speeds) therefore confidence in statistical distribution is high. Reduces staffing costs. Shorter sample run time, more samples run on one instrument, equates to fewer people required to operate an instrument. Decreases reagent requirements. Fewer events are lost so applications can be run with smaller samples, requiring less reagents. Expands instrument usage. Faster sample analysis translates into more customers able to use the instrument. Table 1. MoFlo XDP Benefits Page 6