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Part 1 Exercise

Amino acid tables

Part 1 Summary questions

Part 2 Exercise

Part 2 Summary questions

Computing 2: Bioinformatics Searching

Optional: Search engines

Computing 3: Bioinformatics Project

Interactive discussion

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Computer Exercise 1: Introduction to Virology & Molecular Modeling

Stev 2055 PC lab

Introduction:

Although these exercises are being introduced in both PC and Mac computer labs, the exercises are not platform specific. You may choose to use either Netscape or Explorer as the browser. This introduction is geared [or tries to be] both to those with little experience using the Internet and web browsers, and to those with a significant amount of experience.

If instructions seem to move along too fast, ask for help from other students and from me. If instructions seem too detailed, and you just want to get on with it, please do.

If using the IMac labs, you will need a 100 MB zip disk to save your work. Floppy drives are being fazed out in favor of zip drives. You also may print your work to the printer in the lab you are working.

It is strongly suggested that you keep a log of your sessions on-line. Although you may bookmark sites while using a lab computer, the bookmarks are removed daily. Even if you are using your own computer, try using a log anyway. You can add comments, store specific database sources, and cut/paste whole pages of information for future use. A current version of Word is quite useful for a log, because URLs [Web addresses] can be turned into active link sites. In other words, you can carry your bookmarks with you, without having to retype them. You can save your log to disk or e-mail it to yourself. [For more on logs, go to "Computing", then "Keeping a log".]

There are summary questions at the end of each part. Read them through before you start browsing. You can answer them as you go, or answer them after browsing the following sites. Points = 10. Due 2/19.

The last thing to do is to begin to explore the Interactive site on WebCT. A portion of the discussion points will awarded for on-line participation.

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Part 1: Cool Web Sites

Exercise:

1. Getting to the edge of the pool: Log on and open Netscape. The following web sites are to get you started. Briefly explore each one, noting what they have to offer locally and what links to other sites are available. When using you own computer or one to which you have regular access, I strongly recommend that you bookmark the sites you like. [Bookmarks are regularly removed from school computers, but they are still handy during a single session, so give them a try.

  • Go to All the Virology on the WWW. It is a great place to start and you'll want to come back to explore more on your own. Bookmark what you like. We'll discuss these "finds" in discussion section.

    For now, click on "Big Picture Book of Viruses": There are several ways to search for virus structures here.

    a. Try "virus families by genome type" and look for positive sense RNA viruses. Check out the Picornaviruses.

    b. Try "list of individual viruses" to search by name. Look for Tobamoviruses.

    • Look for differences between these viruses. Examine the surface differences between genera. What types of geometries and patterns do you see?
  • To get an overview of the virus taxonomy and the background which supports it, go to ICTV:

    [This should be quite helpful as we go through the different groups of viruses.]

2. Testing the water: For more on virus modeling, go to Bock Labs.

http://www.bocklabs.wisc.edu/

a. Click on "multimedia library"; then on "computer visualization". Try "analgraphic stereo" & use the 3D glasses for a cool viewing experience.

b. Go back to "computer visualization" page and click on "topographical maps" to learn how the isometric and 3D images are generated from the topology of a single facet or face of the particle surface.

How do the maps help in understanding viral structure? What is the basis of the surface topography?

c. Go back to "multimedia library" and click on "electron micrograph". Explore to see what they have available.

Later, try other subsites of the Bock Labs site to become familiar with what they have to offer.

3. Going for a quick swim on your own: Some sites may initially appear simple, but have rich collections of other sites. They are quite useful. A single bookmark can lead to many hallways and many doors. You'll probably want to revisit these link sites a few times in order to get a real feel of what all they have to offer. Make note in your log of useful destination sites you like. These can be shared. [Also, try going to "Links" for access to these and other useful sites.]

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Part 1 Summary Questions:

Try to limit your answers to one typed page [12 pt font] for this part. [You need not retype the questions as part of your responses.] 

1. [Big Picture Book] What key differences can you identify between Picornaviruses and Tobamoviruses? Compare the surface structure of a polio virus and a rhinovirus. What similarities and differences can you find?

2. Look closely at one of the isometric viruses. What different types of repeating patterns can you detect? What geometries do you see?

3. [Bock Labs] What additional information did you get from the triangular maps? How does it add to your understanding of viral structure?

4. Ultimately, what influences the "texture" of these particles?

5. Give the URLs of two sites you liked which you found by exploring the link sites given in #3 above. Briefly state why you thought they were interesting or how you think they may be of interest to others in class. [I'll summarize these and post them on the "Links" page.] 

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Part 2: Molecular modeling

Exercise:

Time to learn how to explore individual proteins, alone and sometimes in association with other molecules. If you have never played with molecular models, or you want to start with some interactive instruction, begin at 1 below. If you are familiar with modeling and you want to see some viral coat proteins, skip to 2 below.

1. As a warm-up activity to molecular modeling, go to one of the sites below. For either the Kuby text site or the Lodish text site below, click on "molecular visualizations", and select a chapter. As you go through the guided explanation, you'll see different types of displays of the proteins. This will give you an idea of what you can do during this exercise, and after, with proteins of your choice.

http://www.clunet.edu/BioDev/omm/gallery.htm [Online Macromolecular Museum]
http://www.whfreeman.com/kuby
http://www.whfreeman.com/lodish

2. Go to NCBI:

http://www.ncbi.nlm.nih.gov/Structure/

a. Try 1QJY [You can type this accession number into the search line.] It's human rhinovirus 16 coat protein associated with an anti-viral compound. Click on the accession number to open the summary page. Explore this page to see what information is available. To view the protein in Chime/RasMol, go to the bottom of the summary page, select "RasMol", then click on "view".

Once the protein model comes up, click on the MDL prompt in the bottom right corner of the screen to access the command menu. If you are familiar with Chime, play. If you want some help getting started, do the following:

 1)Drag down to "color" and highlight "groups". How many different groups are there in your protein?

2) Drag down to "display" and click on "ribbon". Next, try some of the other display types.

3) Place the arrow on the protein, click and hold down the mouse. As you move the mouse, you can move the protein. As you move the protein around, do you see anything that you couldn't see before?

4) Try marking individual amino acids. For example, select cysteine to locate any disulfide bond sites. Or try to mark amino acids which you would predict as being found on hairpin loops. [See "Shorthand symbols for amino acids" for abbreviations. Chemical characteristics of the amino acids are listed below the symbol table. See a biochem or molecular biology reference for amino acid structures. Or go to "www.whfreeman.com/lodish" for an on-line reference.]

b. Return to the report page of 1QJY. Click on 1QJY to go to another data source page. Explore what is available here. Click on "other sources" to explore further.

c. Open a new window and go to PDBsum [by copy/pasting the URL below] or click below to go directly there:

http://www.biochem.ucl.ac.uk/bsm/pdbsum

Here you can view primary, secondary, and simple tertiary structures of each chain of a protein. The motifs are included in the graphical views, as well as being summarized.

d. Return to the NCBI/ Structure site. Try a new search with either 1RMV [ribgrass mosaic virus] or 2TMV [intact tobacco mosaic virus].

As you explore this protein, note the differences you see when compared to the rhinovirus coat protein.

3. Go back to NCBI/Structure. Type in a virus name, such as polio or another virus of interest; or a family name, such as Leviviridae or Tobamoviridae. Select a protein of interest and explore it as you did the others above. [This will give you a small taste of finding proteins of interest and exploring independently. The next assignment will focus in part on search strategies.

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Part 2 Summary Question:

Try to limit your answer to one typed page [12 pt font] for this part. [You need not retype the questions as part of your responses.] 

Structure determines function. Now that you have gone from BIG [whole virus images] to small [single peptide chain models], write a summary of viral capsid structure as determined by amino acid sequences of the coat proteins involved. Keeping molecular interactions in mind, consider and address the following:

  • What parts of the proteins are involved in self-assembly?
  • How does the assembly occur?
  • Is the presence of nucleic acid required for assembly?
  • How is the capsid structure stabilized?
  • What parts of the capsid are involved in target cell binding?
  • How does binding occur?
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Optional:
For those of you not used to general searching on the web, you should try the following as a way of becoming familiar and comfortable in digging up information and resources of interest.

Look at some general browser search engines, such as Dogpile, Yahoo, and Google [among many others]. When looking for something specific, sometimes you don't quite know where to start; or you thought you did, but came up empty. Sometimes, you just want to find out what is available in a general category. The search engines can be very useful, if you know how to use them efficiently. Different search engines will give different results.

  • Try out a broad term, such as "virology" or "virus", on three different browser search engines. You can pick them from a list, by clicking on "Search" or type in their URLs. I like Yahoo [www.yahoo.com] and Google [www.google.com], because they happen to work well in the science fields, whereas some of the others tend to have more depth in other areas. Dogpile [www.dogpile.com] can search other search engines as a group, therefore can be extremely useful when hunting for hard-to-find items. See what you get on your search in terms of how many hits, and how relevant the top picks are to what you wanted.

  • Try a short string of words or a phrase, such as "virus transmission" or "target cell binding". Try inserting Boolean operators ["and", "or", "not"] between the words to see what effect they have on your search results. Add or subtract some words. Not all search engines work the same way. Some require specific syntax in word strings. Check out their "Help" information on advanced searching. This familiarity will prove useful later on.

 

Introduction to Interactive Virology

Click on "Interactive" below to enter the WebCT portion of this site. Log on with your ID and password. Go to "Fora". Select either the topic "Computer problems" or "Cool new sites" and post a comment or respond to another comment already posted. For more on using WebCT, go to "Computing". Take note of format when entering text. Use double returns between paragraphs, since there is no indenting. Also check spelling and grammar carefully. You can compose off-line in a word processing program, then copy/paste to the text box. This may be advisable if composing a lengthy piece.

 

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 Updated 1/5/02 by thatcher@sonoma.edu