Details
Methods for Fragments Screening Using Surface Plasmon Resonance
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128,39 € |
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| Verlag: | Springer |
| Format: | |
| Veröffentl.: | 15.09.2021 |
| ISBN/EAN: | 9789811615368 |
| Sprache: | englisch |
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Beschreibungen
<p>This volume describes methods and protocols for the fragment-based screening of proteins using Surface Plasmon Resonance (SPR). The initial chapter of the book discusses the principle of SPR for the identification of biomolecular interactions, while the subsequent chapters introduce methods for labelling proteins with different tags including, histidine and biotin tags. It also discusses techniques and factors that affect the amine and biotin-streptavidin coupling and methods to optimize the interactions. Next, it describes fragment preparation for screening in SPR and presents methods to calculate equilibrium dissociation constant (KD) and ligand efficiency (LE). It reviews techniques of next-generation injections that improve the efficiency of the characterization process over traditional SPR by determining the kinetics and affinity in a single step. Finally, the book elucidates a comprehensive yet representative description of challenges associated with the molecular interaction of proteins using SPR.</p><p></p>
<b>Chapter 1</b>_Introduction to SPR.- <b>Chapter 2</b>_ Principle of SPR (OneStep).- <b>Chapter 3</b>_Identification of Fragment library.- <b>Chapter 4</b>_Preparation of protein with Histidine Tag.- <b>Chapter 5</b>_Preparation of protein with Biotin Tag.- <b>Chapter 6</b>_Protein stability using Thermal Shift Assay (TSA) - pH.- <b>Chapter 7</b>_Protein stability using Thermal Shift Assay (TSA) – DMSO.- <b>Chapter 8</b>_Preparation of Sensor.- <b>Chapter 9</b>_ Optimization and validation of Amine coupling.- <b>Chapter 10</b>_ Optimization and validation of Biotin-strepavidin coupling.- <b>Chapter 11</b>_ Preparation of Fragment for Screening in SPR.- <b>Chapter 12</b>_ Screening of Fragment in SPR.- <b>Chapter 13</b>_ Analysis of Data.- <b>Chapter 14</b>_ Identification and arraying of HITS.- <b>Chapter 15</b>_ Confirmation of Hits – Kinetics (kon, koff, KD, LE).<p></p>
<p><b>Dr. Ramachandraiah Gosu</b> is Associate Director, Discovery Biology & Head of Structural Biology Department at Jubilant Biosys Ltd, Bengaluru. His research interests are protein engineering, macromolecular X-ray crystallography and methods for biophysical screening. Before joining Jubilant Biosys, he worked as a post-doctoral fellow at the University of Minnesota, Minneapolis in the Structural Genomics Project- Pathogenic Island Proteins from Staphylococcus aureus. He has obtained his Ph.D. in, Structural Biology from Molecular Biophysics Unit at the Indian Institute of Science, Bangalore, India. He has co-authored several articles in peer-reviewed international journals.</p>
<p><b>Dr. Sameer Mahmood. Z</b> is Group Leader at the Jubilant Biosys Ltd, Bengaluru, India. He has earlier served as Associate Principal Scientist in the Department of invitro biology at GVK Bioscience Ltd, Hyderabad, India, and Principal Scientist I in the Department of Molecular and Cell Biology, Advinus Therapeutics Ltd, Pune. He also did postdoctoral training in the Department of Stem Cell and Molecular Biology at Joslin Diabetes Center (Harvard University), Boston, USA. His research interest is in the high throughput screening of proteins using robotics with specialization in protein-drug (Fragments and Small molecules) interactions. He has been accolade with several awards in Stem cell research, Jackson Laboratory (USA), Asia ARVO (Singapore), Research Achievement Award (USA), CEO award for Excellence in Project Management (India).</p>
He has published several research articles in peer-reviewed international journals and co-authored a book chapter.
<p><b>Dr. Sameer Mahmood. Z</b> is Group Leader at the Jubilant Biosys Ltd, Bengaluru, India. He has earlier served as Associate Principal Scientist in the Department of invitro biology at GVK Bioscience Ltd, Hyderabad, India, and Principal Scientist I in the Department of Molecular and Cell Biology, Advinus Therapeutics Ltd, Pune. He also did postdoctoral training in the Department of Stem Cell and Molecular Biology at Joslin Diabetes Center (Harvard University), Boston, USA. His research interest is in the high throughput screening of proteins using robotics with specialization in protein-drug (Fragments and Small molecules) interactions. He has been accolade with several awards in Stem cell research, Jackson Laboratory (USA), Asia ARVO (Singapore), Research Achievement Award (USA), CEO award for Excellence in Project Management (India).</p>
He has published several research articles in peer-reviewed international journals and co-authored a book chapter.
<p>This volume describes methods and protocols for the fragment-based screening of proteins using Surface Plasmon Resonance (SPR). The initial chapter of the book discusses the principle of SPR for the identification of biomolecular interactions, while the subsequent chapters introduce methods for labelling proteins with different tags including, histidine and biotin tags. It also discusses techniques and factors that affect the amine and biotin-streptavidin coupling and methods to optimize the interactions. Next, it describes fragment preparation for screening in SPR and presents methods to calculate equilibrium dissociation constant (KD) and ligand efficiency (LE). It reviews techniques of next-generation injections that improve the efficiency of the characterization process over traditional SPR by determining the kinetics and affinity in a single step. Finally, the book elucidates a comprehensive yet representative description of challenges associated with the molecular interaction of proteins using SPR.</p>
<p>Discusses real-time and label-free measurement of biomolecular interaction</p><p>Present protocols to calculate kinetics and affinities with single analyte concentration</p><p>Examines techniques for the optimum amine and biotin-streptavidin coupling</p><p>Describes methods to calculate equilibrium dissociation constant (KD) and ligand efficiency (LE)</p>
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