Pharmacological studies in various animal models play a crucial role in early-stage ADC development and afford predictions of therapeutic and safety parameters for subsequent human trials. https://www.creative-biolabs.com/adc/adc-in-vivo-analysis.htm
Presenter: Marina Sirota, UCSF
Recent advances in genome typing and sequencing technologies have enabled quick generation of a vast amount of molecular data at very low cost. The mining and computational analysis of this type of data can help shape new diagnostic and therapeutic strategies in biomedicine. In this talk, I will discuss how such technological advances in combination with data science and integrative analysis can be applied to drug discovery in the context of drug target identification, computational drug repurposing, and population stratification approaches.
Pharmacological studies in various animal models play a crucial role in early-stage ADC development and afford predictions of therapeutic and safety parameters for subsequent human trials. https://www.creative-biolabs.com/adc/adc-in-vivo-analysis.htm
Presenter: Marina Sirota, UCSF
Recent advances in genome typing and sequencing technologies have enabled quick generation of a vast amount of molecular data at very low cost. The mining and computational analysis of this type of data can help shape new diagnostic and therapeutic strategies in biomedicine. In this talk, I will discuss how such technological advances in combination with data science and integrative analysis can be applied to drug discovery in the context of drug target identification, computational drug repurposing, and population stratification approaches.
Current CV .
My objective is to obtain a rewarding and challenging research scientist position where my background and experience will contribute to the success of a growing company or research center.
Currently, I am a Senior Associate Scientist at Amgen Inc. and certified Molecular Biologist with the American Society of Clinical Pathology MB (ASCP). I have more than 10 years of experience in the biotechnology/ pharmaceutical industry. I am highly proficient in various lab techniques, technologies, and automation. I demonstrated consistent success in the execution of assay development and method validation activities supporting clinical stage programs within GCP and GLP regulated environments. I possess extensive experience in optimization and validation of drug potency assays (ELISA and cell based assays), protein purification and characterization, and DNA/RNA extraction and quantitation. I am a subject matter expertise in the areas of human and rodent cell lines propagation and tissue dis-aggregation. I have proven operational capabilities in the establishment of standard operating procedures to ensure our laboratory meets regulatory and business requirements.
I am a self-motivated professional who works effectively as an individual contributor or within a team matrix. As a quick learner, I can efficiently deliver results, easily adapt to changing environment and provide fresh ideas. My strengths include statistical analysis/guidance, report writing, and communication.
Thank you in advance for your consideration. Please feel free to call me at (805-990-6258), or by e-mail at (mahawally46@gmail.com) if you have questions or would like a list of references.
Sincerely,
Maha Rizk
To support research and development in different stages of biopharmaceutical compounds and products, QPS offers biomarker services in different global competence centers using
a wide range of technology platforms to support programs in any therapeutic area. QPS biomarker capabilities range from small molecule analysis to whole cell characterization.
Improving Immunohistochemistry Standardization in your Laboratory: Renewable ...Candy Smellie
What is the impact of assay failure in your laboratory and how do you monitor for it?
To develop genetically defined IHC Reference Standards with consistent protein expression levels for analytic validation and quantitative assessment of immunohistochemistry assays.
Typical molecular biomarkers include proteins, genetic mutations, and aberrant methylation patterns. abnormal transcripts, miRNAs, and other biological molecules. Protein biomarkers are considered reliable indicators of the disease state and clinical outcome as they are the endpoints of biological processes. Remarkable innovations in proteomic technologies in the last few years have greatly accelerated the process of biomarker discovery. https://www.creative-proteomics.com/services/proteomics-service.htm
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Current CV .
My objective is to obtain a rewarding and challenging research scientist position where my background and experience will contribute to the success of a growing company or research center.
Currently, I am a Senior Associate Scientist at Amgen Inc. and certified Molecular Biologist with the American Society of Clinical Pathology MB (ASCP). I have more than 10 years of experience in the biotechnology/ pharmaceutical industry. I am highly proficient in various lab techniques, technologies, and automation. I demonstrated consistent success in the execution of assay development and method validation activities supporting clinical stage programs within GCP and GLP regulated environments. I possess extensive experience in optimization and validation of drug potency assays (ELISA and cell based assays), protein purification and characterization, and DNA/RNA extraction and quantitation. I am a subject matter expertise in the areas of human and rodent cell lines propagation and tissue dis-aggregation. I have proven operational capabilities in the establishment of standard operating procedures to ensure our laboratory meets regulatory and business requirements.
I am a self-motivated professional who works effectively as an individual contributor or within a team matrix. As a quick learner, I can efficiently deliver results, easily adapt to changing environment and provide fresh ideas. My strengths include statistical analysis/guidance, report writing, and communication.
Thank you in advance for your consideration. Please feel free to call me at (805-990-6258), or by e-mail at (mahawally46@gmail.com) if you have questions or would like a list of references.
Sincerely,
Maha Rizk
To support research and development in different stages of biopharmaceutical compounds and products, QPS offers biomarker services in different global competence centers using
a wide range of technology platforms to support programs in any therapeutic area. QPS biomarker capabilities range from small molecule analysis to whole cell characterization.
Improving Immunohistochemistry Standardization in your Laboratory: Renewable ...Candy Smellie
What is the impact of assay failure in your laboratory and how do you monitor for it?
To develop genetically defined IHC Reference Standards with consistent protein expression levels for analytic validation and quantitative assessment of immunohistochemistry assays.
Typical molecular biomarkers include proteins, genetic mutations, and aberrant methylation patterns. abnormal transcripts, miRNAs, and other biological molecules. Protein biomarkers are considered reliable indicators of the disease state and clinical outcome as they are the endpoints of biological processes. Remarkable innovations in proteomic technologies in the last few years have greatly accelerated the process of biomarker discovery. https://www.creative-proteomics.com/services/proteomics-service.htm
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
2. ANAQUANT ‘At a glance’
! Contract Research Organization
! specialized in targeted and absolute protein
quantification by Mass spectrometry,
! offering customized services in assay development
and samples bioanalysis.
! Supports pharmaceutical and biotech companies to speed
up their R&D programs with robust and validated
analytical tools
! ANAQUANT was founded by Tanguy Fortin in 2014 after
more than ten years of research driven by Pr Jérôme
Lemoine at the «Analytical Sciences Institute » of Lyon.
2
3. A purpose for your laboratory
! simplify and accelerate the development of your
bioanalytical tests
! Quickly validate or unvalidate your scientific hypotheses
with limited expenses and risk
! Cross validate your reference method
! Bring additional analytical information like precise
measurement of proteins modifications.
3
Whether you are concerned by upfront research, quality control, or clinical study,
we propose you an orthogonal antibody-free alternative to immunoassay
approach in order to:
4. 3 offers to cover your needs
4
Evaluation, validation
and quantitation of
protein biomarker(s)
tailored to your clinical
question
Absolute and sensitive
quantification of
targeted protein and
homologs in various
biological matrices
Development of assay
to contribute to Critical
Quality Attribute the
definition of
biotherapeutic and the
bioprocess validation
Biomarker Targeted protein
quantitation
Product Quality &
Bioprocess validation
MULTIPLEXING SPECIFICITY ROBUSTNESS
5. 5
Biomarker
! Single or multiplexed
biomarker analysis
(10 to 100 proteins)
! markerQUANT: a analytical tool
developed with the Camille
Jordan Institute, a worldwide
renowned mathematic institute,
to guarantee accurate and
specific results.
! Discovery of biomarkers thanks
to the fullQUANT approach
Main applications
! disease mechanism study
! i d e n t i f i c a t i o n o f n e w
therapeutic targets
! early assessment of drug
efficacy or safety
! identification of your targets in
body fluids
! development of companion
diagnostic test…
6. ! targetQUANT: precise and
absolute quantification of
targeted protein with or
without post-translational
modifications.
! Based on innovative
technology to ensure specificity
and robustness
6
Targeted protein quantification
Main applications
! Level of protein target-ligand
! Early PK/PD assessment
! Measure of post-translational
modification (PTM)
! Cross validation with reference
method
! Transgene expression for gene
therapy drug
! One analysis instead of several
immunoassay kits
7. ! Services based on EMA guidelines
related to biotherapeutics (protein,
Ab, gene therapy, vaccines)
! Goals: to contribute to the Critical
Quality Attribute evaluation of
biotherapeutics & the bioprocess
validation.
! Antibody free analysis to speed up
your bioprocess evaluation
7
Product quality & bioprocess validation
Main applications
! Identity test for Ab, proteins,
vaccines
! Specific proteins degradation
pathways
! Potency tests
! Low levels of impurities (HCPs)
! Biosimilar comparability study
! Bioprocess scale-up comparability
study
8. Our know-know at your services
! Regarding your challenge, your concern, ANAQUANT answers with
customized services.
! Milestones with Go/NoGo decision are established for each project to
secure your budget.
8
Assay
development
Assay validation
Technology
transfer
Sample
bioanalysis
Feasibility study
9. 9
Main advantages of our technology
No antibody
Multiplexing
Absolute quantification
Short assay development time
Minimal sample volume
Biological complex matrices analysis (serum,
plasma, urine, tissue)
10. The added value of our scientific expertise
10
Advices on the protein assay
to implement
Innovative approaches
which improve robustness &
sensitivity of MS analysis
Validated protocols to
control pre-analytical factors
& biological samples
preparation
Method and experience in
data interpretation
Access to:
11. Main publications
! Clinical quantitation of prostate specific antigen biomarker in the low nanogram/mL range by
conventional bore liquid chromatography-tandem mass spectrometry (MRM) coupling and correlation
with ELISA tests
Fortin T, Salvador A, Charrier JP, Lenz C, Lacoux X, Morla A, Choquet-Kastylevsky G, Lemoine J. - Mol Cell Proteomics. 2009
! Multiple reaction monitoring cubed for protein quantification at the low nanogram/milliliter level in
nondepleted human serum.
Fortin T, Salvador A, Charrier JP, Lenz C, Bettsworth F, Lacoux X, Choquet-Kastylevsky G, Lemoine J. - Anal Chem, 2009
! The current status of clinical proteomics and the use of MRM and MRM(3) for biomarker validation
Jérôme Lemoine, Tanguy Fortin, Arnaud Salvador, Aurore Jaffuel, Jean-Philippe Charrier, Geneviève Choquet-Kastylevsky -
Expert Review of Molecular Diagnostics
! Absolute quantification of podocin, a potential biomarker of glomerular injury in human urine, by liquid
chromatography-multiple reaction monitoring cubed mass spectrometry.
Simon R, Lemoine J, Fonbonne C,Jaffuel A, Léonard JF, Gautier JC, Pasquier O, Salvador A. - J Pharm Biomed Anal. 2014
12. To
discuss
about
your
project
please
contact
us:
Tanguy.fortin@anaquant.com
www.anaquant.com