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Source The Cell: Problems Book

When analyzed in detail, the rhythmic beating of a cilium is revealed as a series of precisely repeated movements. In Chlamydomonas the flagellar beat cycle is straightforward (Figure1-A). The beat cycle begins with a power stroke, which is initiated by a bend near the base of the flagellum (arrow at base of flagellum 1 in Figure1-A). The power stroke ends when the bent segment of flagellum extends roughly through half the circumference of a circle (flagellum 5 in Figure1-A). The return stroke is formed by the movement of the semicircular segment of the flagellum outward toward the tip, which is accomplished by further bending at the leading edge of the semicircle and relaxation at the trailing edge (flagella 6 to 8 in Figure1-A).

A. How much sliding of microtubule doublets against one another is required to account for the observed bending of the flagellum into a semicircle? Calculate how much farther the doublet on the inside of the semicircle protrudes beyond the doublet on the outside of the semicircle at the tip of the flagellum (Figure2-A). The width of a falgellum is 180 nm.

B. The elastic nexin molecules that link adjacent outer doublets must stretch to accommodate the bending of a flagellum into a semicircle. If the length of an unstretched nexin molecule at the base of a falegellum is 30 nm, what is the length of a stretched nexin molecule at the tip of a flagellum (Figure2-B)? Adjacent dublets are 30 nm apart.

C. Chlamydomonas mutants that are missing radial spokes have paralyzed flagella. The paralysis can be overcome by mutations in a second gene, which encodes a component of the outer dynein arm. Although the flagella now move, their bear pattern is aberrant(Figure1-B) . At the gross level, how does the aberrant beat stroke of the double mutant differ from that of the wild type? What does this gross difference suggest for the function mediated by the radial spokes in Chlamydomonas ?

Figure 1

Figure 2

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سلام دوستان،

منبع: The Cell:Problems Book

One important parameter for understanding any particular membrane transport process is to know the number of copies of the specific transport protein present in the cell membrane. To measure the number of voltage-gated Na channels in the rabbit vagus nerve, you use a potent toxin, saxitoxin, a shellfish poison that specifically inactivates the voltage-gated Na channels in these nerve cells. Assuming that each channel binds one toxin molecule, the number of Na channels in a segment of vagus nerve will be equal to the maximum number of bound toxin molecules.

You incubate identical segments of nerve for 8 hours with increasing amounts of 125I-labeled toxin. You then wash the segments to remove unbound toxin and measure the radioactivity associated with the nerve segments to determine the toxin-binding curve (upper curve). You are puzzled because you expected to see binding reach a maximum (saturate) at high concentrations of toxin; however, no distinct end point was reached, even at higher concentrations of toxin than those shown in the figure. After careful thought, you design a control experiment in which the binding of labeled toxin is measured in the presence of a large molar excess of unlabeled toxin. The results of this experiment (which is shown in lower curve in the figure) make everything clear and allow you to calculate the number of Na channels in the membrane of the vagus nerve axon.

A. Why does binding of the labeled toxin not saturate? What is the point of the control experiment, and how does it work?

B. Given that 1gram of vagus nerve has an axonal membrane area of 6000 cm2 and assuming that the Na channel is a cylinder with a diameter of 6nm, calculate the number of Na channels per square micrometer of axonal membrane and the fraction of the cell surface occupied by the channel. (Use 100 pmol as the amount of toxin specfically bound to the receptor)

+ نوشته شده توسط دوستان المپیادی! در جمعه نهم بهمن 1388 و ساعت 19:27 |
Salam

bache ha az emrooz fa'aliathaye ABOF ba soalaye to0o0p va dar sathe marhale 2 va 2re aqaz mishe

omidvaram shomam soalaye khoobe2no dar extiare ma bezarin ta ma oona ro bezarim roo site hame Stefade konan

TNX

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+ نوشته شده توسط دوستان المپیادی! در جمعه نهم بهمن 1388 و ساعت 19:22 |
SALAM

inam ye soale jaleb albate be nazare man!!!!
ba garm kardane ab PH va maze an che taqiri mikonad??????????

+ نوشته شده توسط دوستان المپیادی! در پنجشنبه هشتم بهمن 1388 و ساعت 19:50 |
inam az 1 ta 21 lotfan be tartib bahs konim

1- sharayet kam abi

2- qate deraxtane jangali

3-sperm

4-nemoodare photo santez

5- noxae mo0o0sh

6- tariq

7- avande cho0o0b

8- photossantez

9- nitrogen

10-ta'adoli

11- potansiel amal

12-PI
13-14 U shek

15-16 17 18- kerm

19-20 qalb

21- clade

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+ نوشته شده توسط دوستان المپیادی! در پنجشنبه یکم بهمن 1388 و ساعت 19:59 |

inam bahse 2om vase 21 soale 2om

22-23 IRBO13

24- kinesin

25- shajare name

26-27 telomer

28-29 Bv va NPU

30- a be B tabdeil mishe

31- protein A B C

32- aprta

33- hormone X

34- mahi ha

35- shabake qazayi

36- ENglish

37-38- ejtenab

39-40 bi hes konande

41-42 gorbe

mrC
be soala ba tartib javab bedin PLZ

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+ نوشته شده توسط دوستان المپیادی! در پنجشنبه یکم بهمن 1388 و ساعت 19:55 |